Abstract
Fibrocystin/Polyductin (FPC), encoded by PKHD1, is associated with autosomal recessive polycystic kidney disease (ARPKD), yet its precise role in cystogenesis remains unclear. Here we show that FPC undergoes complex proteolytic processing in developing kidneys, generating three soluble C-terminal fragments (ICDs). Notably, ICD15, contains a novel mitochondrial targeting sequence at its N-terminus, facilitating its translocation into mitochondria. This enhances mitochondrial respiration in renal epithelial cells, partially restoring impaired mitochondrial function caused by FPC loss. FPC inactivation leads to abnormal ultrastructural morphology of mitochondria in kidney tubules without cyst formation. Moreover, FPC inactivation significantly exacerbates renal cystogenesis and triggers severe pancreatic cystogenesis in a Pkd1 mouse mutant Pkd1V/V in which cleavage of Pkd1-encoded Polycystin-1 at the GPCR Proteolysis Site is blocked. Deleting ICD15 enhances renal cystogenesis without inducing pancreatic cysts in Pkd1V/V mice. These findings reveal a direct link between FPC and a mitochondrial pathway through ICD15 cleavage, crucial for cystogenesis mechanisms.
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Introduction
Polycystic kidney disease (PKD) refers to a collection of genetic disorders characterized by the development of kidney cysts originating from the renal tubules, often accompanied by the growth of cysts in the hepatic and pancreatic ducts1. These cysts disrupt the renal parenchyma, leading to filtration obstruction and eventual kidney failure. PKD presents in two major forms, each with similar yet distinct pathological features: autosomal recessive polycystic kidney disease (ARPKD) and autosomal dominant polycystic kidney disease (ADPKD)1,2.
ARPKD, affecting 1 in 20,000 live births, is typically diagnosed in utero or shortly after birth3. It is characterized by bilateral cystic enlargement of the kidneys and congenital hepatic fibrosis4. During early fetal development, the ARPKD kidney undergoes a transient phase of proximal tubule cyst formation, but as fetal stages progress, the site of cystic dilation shifts to distal tubules5. The typical renal pathology in postnatal specimens is non-obstructive fusiform dilatation of the collecting ducts. ARPKD is primarily caused by mutations in polycystic kidney and hepatic disease 1 (PKHD1) gene6,7, although pathogenic variants in other genes have also been associated with ARPKD-like phenotypes4,8. The PKHD1 gene produces a full-length transcript consisting of 67 exons that encode a protein called Fibrocystin/Polyductin (FPC) of 4074 amino acids (aa). The specific function of FPC and its role in cystogenesis are still unknown6,7.
FPC is a receptor-like single transmembrane (TM) glycoprotein with a short cytoplasmic C-terminal tail that contains various motifs including a ciliary targeting sequence (CTS)9 and nuclear translocation signal (NLS)10,11. It is primarily expressed in renal tubular structures, particularly in the collecting ducts and the thick ascending limb of the loop of Henle, with lower levels observed in the proximal tubules12,13,14,15. FPC has been reported to localize to primary cilia, and other subcellular compartments12,13,15,16. Studies using recombinant FPC10,11 and epitope-tagged Pkhd1 knock-in mouse models14,17 have shown that a subset of FPC undergoes complex Notch-like proteolytic cleavage. Cleavage in the extracellular region at a putative proprotein convertase site KRKR3613↓N (↓ denotes scissile bond) results in a soluble extracellular domain (“PECD”) that remains associated with the TM-containing C-terminal fragment (“PTM”) by disulfide bonds11,14 or is secreted into urine11,17. Further intramembrane cleavage leads to the generation of one or multiple intracellular C-terminal domain fragments (“ICDs”), which may translocate into the nucleus and play a role in transcriptional regulation10,11. The exact processing pattern of native FPC and its functional implications are still unknown.
ADPKD is a more common condition, affecting 1 in 500–1000 individuals, and it typically manifests later in life18. This condition is characterized by the development of focal cysts originating from all segments of the renal tubules. The majority of ADPKD cases are caused by mutations in PKD1 (~78%) or PKD2 (~15%), which encode polycystin-1 (PC1) or polycystin-2 (PC2), respectively (“polycystins” collectively)1,2. PC1 is a 4302-aa atypical G-protein coupled receptor (GPCR) with 11 transmembrane domains, an extensive extracellular region, and a short cytoplasmic C-terminus. It plays an essential role in tubular morphogenesis19. Pkd1 knockout mice develop severe cystic kidney and pancreas, culminating in embryonic lethality20,21. The protein is functionally regulated by cis-autoproteolytic cleavage at the juxtamembrane GPCR Proteolysis Site (GPS) within the GPCR-Autoproteolysis INducing (GAIN) domain22,23,24. Pkd1V/V knock-in mice, which carry the T3041V mutation at the cleavage site of GPS, display impaired cleavage of the PC1 protein and develop PKD after birth23,24. PC1 can form a complex with PC2, a member of the transient receptor potential family. This complex is thought to function as a non-selective cation channel at the primary cilium and plasma membrane25,26.
The regulation of mitochondrial ultrastructure is crucial for optimal mitochondrial function, affecting oxidative phosphorylation and overall metabolic capacity27. Dilated cristae have been linked to defective assembly of respiratory chain complexes in supercomplexes, resulting in reduced respiratory efficiency, impaired cellular metabolism, and decreased cell viability28. In ADPKD, metabolic reprogramming and mitochondrial dysfunction are significant contributors to disease pathogenesis29,30, modifying renal cyst growth in Pkd1 mouse models31,32. Polycystins were found to localize to the mitochondria-associated ER membranes33 and potentially contribute to the regulation of Ca2+ uptake in mitochondria33,34,35. PC1 may directly impact mitochondrial function and cystogenesis by translocating a small C-terminal cleavage product into the mitochondrial matrix36,37 and indirectly by inhibiting miR-17 and modulating mitochondrial morphology38. Pathogenic PKHD1 truncating mutations introduced into human embryonic kidney HEK293 cells led to significant structural and functional mitochondrial abnormalities39. Despite these findings, a consensus has not been reached concerning the role of mitochondria in PKD.
Various Pkhd1 mutant mouse models have been developed to investigate the function of FPC and its role in ARPKD. However, these orthologous mouse mutants15,40,41,42, including the Pkhd1 knockout strain Pkhd1LSL/LSL17 (referred to as Pkhd1 KO) and the hypomorphic Pkhd1Δ3-4/Δ3-4 mutant carrying a deletion of exons 3–414,43 (Table 1), display minimal renal disease. Instead, these models develop varying degrees of biliary dysgenesis or pancreatic cysts in a subset of adult animals, but not during development15,17,40,43. Notably, the Pkhd1Δ67/Δ67 mutant strain, with a deletion of exon 67 encoding the last 137 aa of the 185-aa C-terminal tail, exhibits no extra-renal abnormalities14. The reason for the limited renal pathologies remains unclear. Investigation of Pkhd1 mutations on a Pkd1 mutant background reveals a genetic interaction between the two genes in cystogenesis43,44. In a recent study by Olson et al.45, a digenic model combining the Pkhd1 KO strain with the hypomorphic Pkd1RC/RC mutant displayed an ARPKD-like phenotype characterized by rapidly progressing PKD and early lethality. The study found no evidence of physical interaction between FPC and polycystins, suggesting independent functions that synergistically contribute to cystogenesis via a cilia-dependent mechanism45.
In this study, we have investigated the intricate processing of endogenous FPC in developing kidneys and its impact on mitochondrial function and cyst formation in mice. We report that complex proteolytic processing of FPC generates three soluble C-terminal fragments. Among these fragments, ICD15 was found to translocate into mitochondria through a mitochondrial targeting sequence located at its N-terminus. We investigated the functional consequences of FPC inactivation on mitochondrial respiration and analyzed the effects of ICD15 translocation into mitochondria on mitochondrial function in cultured renal epithelial cells. We also analyzed the ultrastructural morphology of mitochondria in the Pkhd1 KO kidneys despite the absence of cystic phenotype. Through genetic epistasis analyses of three Pkhd1 mouse mutants with the hypomorphic Pkd1V/V mutation, we elucidated the role of FPC and the functional significance of its ICD15 in cystogenesis during development. Our findings establish a direct connection between the ciliary FPC protein and mitochondria facilitated by ICD15 through proteolytic cleavage, shedding new light on the function of FPC in cystogenesis in conjunction with PC1.
Results
Complex processing of native FPC resulting in C-terminal fragments in vivo
To investigate the role of proteolytic cleavage in native FPC, we examined the cleavage pattern of endogenous FPC in developing kidneys using a panel of anti-FPC antibodies through western blot analysis (Fig. 1a). The E1 antibody specifically recognizes an epitope within the C-terminal 137 amino acids encoded by the final exon, exon 6714. Additionally, we have developed two new rat monoclonal antibodies, E3 and E4, which target distinct epitopes within the extracellular region of mouse FPC. E3 is directed towards the PECD region, while E4 specifically targets the PTM region.
E1 antibody detected the ~500 kDa full-length FPC (indicated with “a” in Fig. 1b) as well as the ~50–55 kDa PTM product (“c”) in P6 wild-type (WT) mouse kidney lysates, consistent with previous findings11,14. The antibody also recognized a novel product of ~190 kDa (indicated by “b”). Additionally, E1 detected three small fragments (indicated by “d”, “e” and “f”). These products were not observed in kidney lysates from Pkhd1 KO mice, indicating that they are specific FPC products containing the C-terminal region. To confirm the observed FPC processing pattern, we utilized the Pkhd1Flox67HA knock-in model, which incorporates a 3xHA epitope tag at the C-terminus of FPC14. In the Pkhd1Flox67HA kidneys, the E1 antibody identified a matching set of six FPC products, with the four smaller products exhibiting slightly slower migration compared to the untagged FPC products detected in WT kidneys (Fig. 1b). These products were also specifically recognized by anti-HA antibody, but not in WT and KO samples, confirming the presence of the 3xHA tag (~4.4 kDa) and providing an explanation for the observed slower migration of the smaller products. This outcome validates the in vivo cleavage pattern of FPC in developing kidneys. Importantly, the presence of the C-terminal 3xHA tag enables us to further conclude that the three ICD fragments share the same C-terminal amino acid sequence but have different N-termini, likely resulting from distinct cleavage events.
To map the N-termini of these ICD fragments more accurately than was possible with a standard protein ladder, we designed a molecular ruler consisting of constructs beginning with methionine (Met) residues within the ICD (Fig. 1c, d). By using this ladder as a reference, the largest ICD fragment (“d”, ~15.3 kDa, designated ICD15) aligned approximately with the M0 or M1 construct beginning at position 3920 or 3924 respectively, the next fragment (“e”, ~11.9 kDa, designated ICD12) aligned closely with the MC construct starting at position 3953, and the smallest fragment was smaller than any of our ladder constructs (“f”, ~6.3 kDa, designated ICD6). Figure 1f schematizes all six FPC products, including the ICD products found in developing kidneys.
To gain insights into the functional role of these C-terminal products, we performed in silico analyses for this region of FPC. Using MitoProt II46, we identified a potential mitochondrial targeting sequence (MTS) located at the N-terminus of ICD15 (Fig. 1d). In mouse FPC (mFPC), the MTS spans amino acids Met3924-Leu3952, while in human FPC (hFPC), it encompasses amino acids Met3930-Ala3966, with probability scores of 0.3943 and 0.9799, respectively (Fig. 1e). The MTS partially overlaps with the nuclear localization signal (NLS) by seven amino acids. Notably, the sequence of ICD15 is entirely encoded by exon 67 (Fig. 1d). The relationship between these targeting sequences and the three ICD products is schematized in Fig. 1f.
We next investigated the processing of endogenous FPC in the extracellular region using E3 and E4 antibodies (Fig. 1g). Both antibodies detected full-length FPC in WT and Pkhd1+/- kidney samples, similar to E1 antibody. However, no signal was observed in the Pkhd1 KO samples, confirming the specificity of these newly developed antibodies (Fig. 1g). However, E3 did not recognize any fragments shorter than full-length FPC that were detected by the E1 antibody. This suggests that once generated by cleavage, the PECD is not significantly accumulated in the developing kidneys and may mostly be secreted in the urine11,14,17. On the other hand, the E4 antibody detected a small quantity of the shorter fragments that are also recognized by the E1 antibody (Fig. 1g, “b”, “c”). These results suggest that in vivo, only a subset of native FPC molecules are processed at the putative proprotein convertase site, resulting in an abundance of the full-length form, a small amount of PTM product, and minimal accumulation of PECD.
The labeling pattern of E1, E3, and E4 antibodies was also investigated for FPC in kidneys derived from Pkhd1Δ67/Δ67 (referred to as ΔCT hereafter), which lack exon 6714. As anticipated, E1 did not detect any FPC products in the mutant kidneys (Fig. 1g). In contrast, both E3 and E4 antibodies detected a mutant form of FPC in ΔCT kidneys, which was similar in size to, but less abundant than, the full-length FPC present in WT and Pkhd1 + /- samples (Fig. 1g). Our data indicate that the ΔCT mutant expresses a truncated FPC protein, FPC-ΔCT, which lacks the ICD15 region but retains the intact extracellular region, transmembrane domain, and adjacent ciliary targeting sequence. The functional significance of the ICD15 region will be described later in the study.
FPC ICD15 translocates to mitochondria through an unmasked N-terminal mitochondrial targeting sequence
Given that classical MTSs are typically located at the N-terminus of proteins47, we hypothesized that the predicted MTS in full-length FPC might be masked or inaccessible. We further hypothesized that cleavage events leading to the generation of ICD15 could expose the MTS at the N-terminus, thereby facilitating the mitochondrial import of this cleavage product. To test this hypothesis, we generated human and mouse constructs of ICD15 tagged with GFP at the C-terminus and assessed their localization upon transfection in mIMCD3 (murine inner medullary collecting duct) cells (Fig. 2a–d). Both the human (Fig. 2b, hICD15-GFP) and mouse (Fig. 2c, mICD15-GFP) constructs localized to mitochondria, along with some weak nuclear and cytoplasmic staining. In contrast, when a mutant mouse ICD15 construct (mICD15-Mut-GFP) with a mutation in the MTS region that reduces the probability of mitochondrial import was examined (Fig. 2a), it displayed a complete loss of mitochondrial accumulation and instead exhibited strong nuclear localization (Fig. 2d). This observation strongly suggests that the N-terminal MTS of ICD15 is crucial for its translocation into mitochondria. Notably, the human ICD15-GFP construct demonstrated a more robust mitochondrial accumulation compared to the mouse construct, which appeared more diffused. This is consistent with the higher probability score for mitochondrial import in the human MTS sequence (0.9799) compared to the corresponding mouse sequence (0.3943) (Fig. 1e).
We then used a split GFP complementation assay48 to validate the mitochondrial import of ICD15 (Fig. 2e–j). In this assay, the first 10 β-strands of GFP (GFP1-10) were fused with mCherry and targeted to mitochondria through a mitochondria-targeting sequence (MTS-mCherry-GFP1-10), while the 11th β-strand (GFP11) was fused to the ICD15 (ICD15-GFP11) for assessment (Fig. 2e). Mitochondrial GFP fluorescence would only occur if ICD15-GFP11 is translocated into mitochondria and spontaneously assembles with the MTS-mCherry-GFP1-10. When mouse ICD15-GFP11 (mICD15-GFP11) and MTS-mCherry-GFP1-10 were co-transfected into mIMCD3 cells, we observed strong green fluorescence complementation specifically in mCherry-labeled mitochondria (Fig. 2f). Similarly, the human ICD15-GFP11 construct demonstrated robust reconstitution of GFP fluorescence within mitochondria (Fig. 2g). Co-transfection with the GFP11 construct lacking the ICD15 portion did not produce green fluorescence, despite the observation of mCherry fluorescence within the mitochondria (Fig. 2j).
To further confirm the role of the MTS in ICD15 for mitochondrial translocation, we introduced specific mutations in the MTS region of the human ICD15-GFP11 construct (hICD15-GFP11), designed to decrease the probability of mitochondrial import, as predicted by MitoProt II. Substituting Arg3931 and K3933 with Glu (Mut1), which decreased the probability of mitochondria import from 0.9799 to 0.0428 (Fig. 2a), resulted in reduced GFP fluorescence complementation as evidenced by weakened mitochondrial GFP signal (Fig. 2h). Additional replacement of Met3935 and Val3939 with Glu (Mut2), which further reduces the import probability to 0.0226, completely abolished the mitochondrial GFP signal (Fig. 2i). A weak diffuse cytosolic GFP signal was occasionally observed for the MTS mutants, possibly because they interacted with the newly synthesized GFP1-10 construct outside of mitochondria. Collectively, these findings provide compelling evidence for the essential role of the MTS in mediating the translocation of ICD15 into mitochondria.
We next characterized the ICD12 and ICD6, which lack the MTS. For this purpose, we generated stable MDCK (Madin-Darby canine kidney) cell lines expressing the transmembrane C-terminus of mouse FPC (TMCT, aa 3852–4059, see Fig. 1d) to allow posttranslational cleavage. We performed a cellular fractionation to enrich for mitochondria and detected bands corresponding to ICD15, ICD12, and ICD6 in the mitochondrial fraction, but not in the cytoplasmic fraction (Fig. 2k). These bands were absent from the control cells. This result suggests that ICD12 and ICD6 are likely derived from ICD15 within the mitochondria.
Role of FPC in mitochondrial function and the functional impact of ICD15 in cultured renal epithelial cells
To investigate the potential function of FPC and the role of ICD15 in mitochondria, we inactivated Pkhd1 in mIMCD3 cells by employing CRISPR technology and evaluated the effect on mitochondrial function (Fig. 3). We observed that the Pkhd1 knockout (KO) cells displayed a significant reduction in oxygen consumption rate (OCR) compared to the wild-type control (CT) mIMCD3 cells, as determined by a standard Mito Stress Test conducted on a Seahorse flux analyzer (Fig. 3a). This result indicates that the inactivation of FPC directly contributes to significant alterations in mitochondrial function, thus suggesting a crucial role of FPC in the regulation of mitochondrial function.
To assess the functional significance of ICD15 on mitochondria, we stably expressed mouse ICD15 constructs (ICD15 or ICD15-Mut) in mIMCD3 Pkhd1 KO and CT cells using the PiggyBac transposon system25,49 (Fig. 3b) and evaluated their impact on OCR (Fig. 3c). Remarkably, the expression of ICD15 in Pkhd1 KO cells resulted in a modest but significant increase in maximal respiration and spare respiratory capacity when compared to Pkhd1 KO cells. Conversely, the expression of ICD15-Mut, which has reduced mitochondrial translocation (Fig. 2a, d), had a minimal or marginal impact on these parameters (Fig. 3c). These findings indicate that ICD15 can enhance mitochondrial respiration through mitochondrial translocation, partially compensating for the impairment of mitochondrial function caused by Pkhd1 deficiency.
Significantly, the expression of the ICD15 construct also increased OCR in the CT cells, both in terms of maximal respiration and spare respiratory capacity, compared to the CT cells (Fig. 3c). Notably, the increase observed as a result of the mitochondrial translocation of the ICD15 construct was more pronounced in CT cells than in Pkhd1 KO cells. In contrast, minimal to no effects on OCR were observed with the ICD15-Mut construct when compared to CT cells. These findings strongly suggest that ICD15 plays a crucial role in enhancing mitochondrial function in renal epithelial cells, and its functional impact is dependent on its translocation into the mitochondria.
Altered mitochondrial ultrastructure in Pkhd1 KO mice
We examined mitochondrial ultrastructural morphology in the renal tubules of Pkhd1 KO and WT littermate controls using transmission electron microscopy (Fig. 4a–d). Focusing on PTs known for their high ATP demands and susceptibility to mitochondrial dysfunction50, we imaged three P6 kidneys per genotype. A total of 962 mitochondria were compared for each genotype, from 3–5 proximal tubules per kidney. Mitochondrial morphology was evaluated using the following established mitochondrial shape descriptors51: surface area, perimeter, circularity [4π(surface area/perimeter2)], and solidity [(area/convex area)]. Circularity indicates the degree of resemblance to a perfect circle (with a value of 1), while solidity measures the concavity or convexity of a shape, reflecting its complexity and branching. Measurements were obtained from images blinded from genotype.
Despite the absence of a cystic phenotype, we observed significant differences in mitochondrial size between Pkhd1 KO samples and their WT littermate controls. KO mitochondria exhibited a smaller surface area (p = 0.0080) (Fig. 4e) and perimeter (p = 0.0002) (Fig. 4f) compared to WT littermate mitochondria. Additionally, KO mitochondria displayed a more rounded shape (p = 0.0062) (Fig. 4g) compared to WT mitochondria. However, there was no significant difference in branching, as measured by solidity, between WT and KO mitochondria (p = 0.9643) (Fig. 4h). These structural alterations suggest a higher degree of mitochondrial fragmentation in KO kidney tubular cells.
Furthermore, aberrantly shaped mitochondria in KO proximal tubules (Fig. 4j, l) exhibited distinct changes in cristae diameters compared to WT mitochondria (Fig. 4i, k). Analysis of 50 mitochondria from each group showed that KO mitochondria exhibited significantly swollen cristae, with an average diameter of 20.24 nm, compared to the WT average of 19.06 nm (p = 0.0191) (Fig. 4m). This finding suggests an impairment in the inner mitochondrial membrane in KO mitochondria. Taken together, our results provide compelling evidence suggesting that FPC likely plays a role in regulating both the structure and function of mitochondria in the tubular cells of the kidney.
Disruption of FPC enhances the cystic kidney phenotype of non-cleavable Pkd1 mutant, Pkd1 V/V
To investigate the role of FPC and the functional significance of the ICD15 in cystogenesis, we conducted genetic epistasis analysis by combining Pkhd1 mutant strains with the hypomorphic Pkd1V/V knock-in mouse mutant24 (Table 1). The Pkd1V allele, which expresses a non-cleavable PC1V mutant, was specifically chosen for its unique effects on cystogenesis in specific nephron segments and developmental stages. This allele has been shown to rescue cystogenesis in the embryonic kidney and pancreas, preventing embryonic lethality24. Moreover, it provides protection to proximal tubules (PTs), while allowing cystic dilation in distal nephron segments and collecting ducts (CDs) postnatally, ultimately leading to kidney failure and death around 3 weeks of age24. We hypothesized that these distinctive characteristics exhibited by the Pkd1V allele would significantly facilitate the identification of the specific contributions of FPC and the impact of ICD15 on cystogenesis.
We initially examined the phenotypic impact of the hypomorphic Pkhd1Δ3-4 allele on the Pkd1V/V mutants by comparing the phenotypes of the Pkhd1Δ3-4/Δ3-4 (Δ3–4 hereafter) or Pkd1V/V single mutants with the digenic mutant mice. Histologically, at postnatal day 0 (P0), the kidneys of Δ3–4 mutants (Fig. 5b) appeared similar to their WT littermates’ kidneys (Fig. 5a), as confirmed by lectin staining (Fig. 5f, Δ3–4; Fig. 5e, WT). The Pkd1V/V kidneys exhibited intact proximal tubules (marked by Lotus tetragonolobus lectin, LTL, green) and displayed slight cystic dilation in the CDs (marked by Dolichos biflorus agglutinin, DBA, red) at this stage (Fig. 5d, h). Both digenic Pkhd1Δ3-4/+;Pkd1V/+ heterozygous mutants and Pkhd1Δ3-4/Δ3-4;Pkd1V/+ trans-mutants were fertile and appeared indistinguishable from the WT animals. Therefore, we performed a series of intercrosses either between the digenic heterozygous mutants (Pkhd1Δ3-4/+;Pkd1V/+) or between the trans-mutants (Pkhd1Δ3-4/Δ3-4;Pkd1V/+). Breeding resulted in a total of 93 pups from 16 litters with only three digenic homozygous animals (Pkhd1Δ3-4/Δ3-4;Pkd1V/V, denoted as Δ3–4/V hereafter) surviving to birth. Histologic examination of these rare Δ3–4/V pups revealed extensive PT and CD cystic dilation throughout the entire kidney, with little parenchyma remaining (Fig. 5i, m). We observed occasional glomerular cystic expansion in the Δ3–4/V mutants (indicated by the green arrow), which was not observed in any of the single mutants. Next, we examined the embryonic stages for gross pathology. The Δ3–4/V embryos that survived to embryonic day 17.5 (E17.5) showed extensive renal cystic dilation in both PT and CD and occasional glomerular cysts (Fig. 5j, n). Δ3–4/V kidneys exhibited cystic dilation in both PT and CD at E16.5 (Supplementary Fig. 1a, b) with slight dilations beginning to appear at E15.5 (Supplementary Fig. 1d). Pkd1V/V mice did not exhibit any abnormalities in the PT and showed negligible dilations in the CD starting around E16.5 (Supplementary Fig. 1g). These findings show that the combined Pkhd1Δ3-4/Δ3-4 and Pkd1V/V mutations result in a more severe kidney phenotype reminiscent of Pkd1 null mutants20,52.
To test the possibility of Pkhd1 having an additional role in cystogenesis that may not have been fully uncovered with the hypomorphic Pkhd1Δ3-4 allele, we examined the phenotypic effects of the Pkhd LSL KO allele17 on the Pkd1V/V mutants. The Pkhd LSL/LSL (KO) single mutants did not show any significant kidney abnormalities as expected (Fig. 5c, g). We performed a series of intercrosses similar to those performed with the Pkhd1Δ3–4 allele. Breeding resulted in a total of 136 pups from 19 litters with only 6 digenic homozygous Pkhd1LSL/LSL;Pkd1V/V mutants (referred to as KO/V) surviving to birth. The digenic KO/V mutants developed severely cystic kidneys at postnatal day 0 (P0) (Fig. 5k, o), similar to the Δ3–4/V mice (Fig. 5i, m). Cyst development was evident at the embryonic stages of E17.5 (Fig. 5l, p) and E16.5 (Supplementary Fig. 1j). PT and CD cysts appeared in all stages and occasional glomerular cysts were also noted (Fig. 5k, l, green arrows). Therefore, like the Δ3–4/V, the KO/V mutants display a severe Pkd1 null-like cystic kidney phenotype20,52.
To understand the basis for the similar phenotype of the Δ3–4/V and the KO/V kidneys, we compared FPC protein expression in KO, Δ3–4, and WT kidneys. Using the E1 antibody, we detected a ~ 500 kDa mutant FPC in Pkhd1Δ3–4/Δ3–4 kidneys that is similar in size to, but far less abundant than, the full-length FPC in WT sample, but not in the KO sample (Fig. 5q)14. The mutant FPC likely contains a deletion of 123 amino acids in the extracellular domain, presumably encoded by a minor mutant transcript previously identified in Pkhd1Δ3-4/Δ3-4 kidneys43. These findings indicate that Pkhd1Δ3-4 represents a severely hypomorphic allele, which provides an explanation for the observed phenotypic similarities observed between the Δ3–4/V and KO/V mutants.
In summary, the loss of FPC in hypomorphic Pkd1V/V mice results in a kidney phenotype similar to the Pkd1 null condition, with cystic expansion in glomeruli, proximal tubules, and accelerated cyst growth in distal tubules and collecting ducts. These results reveal the protective role of Pkhd1 in maintaining the architecture of both the proximal tubule and distal tubule/collecting duct lumens during kidney development.
Expression level and intracellular trafficking of mutant PC1 are not altered by FPC inactivation in developing kidneys
PC1 plays a central role in cyst formation in a genetic interaction network for polycystic kidney and liver diseases44,53. Proper functioning of PC1 requires cleavage at the GPS, resulting in PC1NTF and PC1CTF products that remain non-covalently associated, coexisting with a small amount of the uncleaved form, PC1U22,24,54. To elucidate the mechanisms underlying the genetic interaction between Pkhd1 and Pkd1 in kidney cystogenesis, we examined whether the loss of FPC alters the expression and cleavage of PC1. To address this, we performed western blot analysis on P6 kidneys from Pkhd1 KO and WT littermates using the E8 antibody55,56 (Fig. 5r). The E8 antibody specifically recognizes a region in PC1CTF, thereby detecting both PC1U and PC1CTF on the western blot. This feature enables the assessment of the overall level of PC1 and the extent of cleavage by analyzing the signal ratio of PC1CTF to PC1U forms56. We found that the levels and ratios of PC1CTF and PC1U were comparable between the Pkhd1 KO and WT kidneys (Fig. 5r, left panel “Kidney”), consistent with the findings reported by Olson et al45. To ascertain that the effects of Pkhd1 inactivation were specific to renal tubules and not confounded by PC1 expression outside of renal tubules of the kidney, we also isolated intact renal tubule fragments and analyzed them separately. We found that the levels and ratios of PC1CTF and PC1U were also similar in the isolated renal tubules from Pkhd1 KO and WT kidneys (Fig. 5r, left panel “Tubule”). The renal tubule preparation was validated by imaging and a set of nephron fragment-specific markers (Fig. 5r, right panel). These data indicate that Pkhd1 inactivation does not affect the level and GPS cleavage of PC1 in kidney tubules.
To determine if the non-cleavable PC1V mutant is more susceptible to Pkhd1 inactivation, we compared the level of PC1V in the kidneys of Pkd1V/+ and Pkhd1Δ3-4/Δ3-4;Pkd1V/+ littermates using western blot analyses. These kidneys were chosen specifically because they exhibit a structurally normal phenotype, allowing for an accurate assessment of the effect on PC1V without the confounding factors of cyst development. Using the E8 antibody, we detected two distinguishable bands of over 500 kDa in size in both samples, with the lower band comigrating with the less abundant PC1U, which is exclusively detected in the WT control (Fig. 5s). To differentiate between PC1V and PC1U in these samples, we took advantage of their differential glycosylation patterns. PC1V acquires partial resistance to Endoglycosidase H (EndoH) digestion, while PC1U remains entirely EndoH-sensitive22,54. Our N-glycan analysis using EndoH and PNGase F confirmed that the upper band in the two samples exclusively corresponded to the EndoH-resistant form of PC1V (PC1V-R), while the lower band primarily represented the EndoH-sensitive form of PC1V (PC1V-S), with a minor contribution of PC1U (Fig. 5s). We found similar levels of both PC1V-R and PC1V-S between the Pkd1V/+ and Pkhd1Δ3-4/Δ3-4;Pkd1V/+ kidney samples (Fig. 5s). These results suggest that the inactivation of Pkhd1 does not significantly affect the expression level or intracellular trafficking of PC1V in developing kidneys. Our findings indicate that the Pkd1 null-like phenotype observed in the digenic mutants is not attributed to a reduction in the level or maturation of PC1V. Other factors or mechanisms may contribute to the observed phenotype in the digenic mutants.
Deletion of Pkhd1 exon 67 enhances renal cystogenesis of Pkd1 V/V mutant mice but does not induce pancreatic cyst formation as observed with Pkhd1 inactivation
We next investigated the potential role of mitochondria-associated ICD15 in cystogenesis by performing an epistatic analysis. For this purpose, we utilized the Pkhd1Δ67/Δ67 mutant strain, which specifically lacks the ICD15 amino acid sequence (Table 1; Fig. 1g), in combination with the Pkd1V/V mutant strain. We performed intercrosses between digenic Pkhd1Δ67/+;Pkd1V/+ heterozygotes or between the Pkhd1Δ67/Δ67;Pkd1V/+ trans-mutants to generate the digenic homozygous animals Pkhd1Δ67/Δ67;Pkd1V/V (denoted as ΔCT/V). Breeding resulted in a total of 192 pups from 28 litters with 26 ΔCT/V animals surviving to birth, corresponding roughly to Mendelian ratios. We found that, unlike the neonatal lethal KO/V and Δ3–4/V mutants, the ΔCT/V survived an average of 20 days postnatally. We examined 13 ΔCT/V kidneys at P0. Significantly, whilst ΔCT single homozygote kidneys were cyst-free (Fig. 6b, e), resembling WT kidneys (Fig. 6a, d), ΔCT/V mice had developed numerous discernible renal cysts (Fig. 6c, f), though to a lesser extent than KO/V and Δ3–4/V embryos. The cystic area of ΔCT/V kidneys was significantly greater than that of WT and ΔCT, which were indistinguishable by this measurement, or that of Pkd1V/V (V) (Fig. 6g). Significantly, like in KO/V and Δ3–4/V embryos, lectin staining revealed that these cysts also developed from proximal tubule and collecting duct origins (Fig. 6f). However, glomerular cysts were uncommon in the ΔCT/V mutants, reflecting either the reduced severity of the cystic state or a lack of importance of ICD15 in maintaining the Bowman’s capsular space. At P6, the ΔCT/V mice showed cystic dilation extended to the entire kidney similar to the Pkd1V/V, but also significant PT dilation that is absent in the Pkd1V/V single mutants (Supplementary Fig. 1k, l). Taken together, our data provide strong evidence supporting the critical role of the mitochondria-associated ICD15 product in regulating renal cystogenesis, in conjunction with PC1, during development.
Lastly, we examined the role of FPC and the impact of ICD15 in cystogenesis within the liver and pancreas by analyzing their phenotypes of the Δ3–4/V, KO/V, and ΔCT/V digenic mutants during development. In the liver, we did not observe any apparent abnormalities in either the digenic or single mutants (Supplementary Fig. 1a, c, d–f, i, j). This contrasts with the findings reported in non-orthologous murine models of ARPKD57. However, due to perinatal death, we were unable to examine hepatic fibrosis at a later stage. In the pancreas, both Δ3–4/V and KO/V mutants exhibited extreme cystic expansion, leading to the formation of a single central cystic lumen and the obliteration of the parenchyma at E17.5 (Fig. 6m, n). This cystic pancreatic phenotype was also observed in the digenic mutants as early as E15.5 (Supplementary Fig. 1d-f), with only a small amount of remaining parenchyma at the periphery. This phenotype closely resembles that observed in the Pkd1 mutant embryos20. However, the pancreas in the ΔCT/V mice remained intact at E17.5 (Fig. 6o), appearing similar to the WT (Fig. 6h) and the single mutants (Fig. 6i–l; Supplementary Fig. 1h,i). Our findings demonstrate that, while FPC plays a crucial role in cystogenesis in the pancreas, its ICD15 does not have a substantial impact on this process when combined with the Pkd1V/V mutation.
Discussion
In our study, we made significant discoveries regarding the role of FPC and its C-terminal cleavage product ICD15 in mitochondria and cystogenesis. We found that ICD15 contains a mitochondrial targeting sequence (MTS) at its N-terminus (Fig. 1), which directs its translocation into mitochondria (Fig. 2). ICD15 enhances mitochondrial respiration in cultured renal epithelial cells through mitochondrial translocation and partially restores the impaired mitochondrial function resulting from the loss of FPC (Fig. 3). Furthermore, we observed significant ultrastructural abnormalities in the mitochondria of Pkhd1 knockout kidney tubules despite the absence of a cystic phenotype (Fig. 4). Moreover, we found that the loss of FPC in hypomorphic Pkd1V/V mouse mutants resulted in a severe cystic phenotype in the kidney and pancreas during development, closely resembling the phenotype of Pkd1 null mice (Figs. 5, 6). Specific deletion of exon 67, which encodes the ICD15 amino acid sequence, enhances cystogenesis in the kidney but not in the pancreas of Pkd1V/V mice (Fig. 6), supporting a significant role of ICD15 specifically in kidney cyst formation. Overall, our findings establish a crucial connection between FPC and mitochondria, likely mediated by ICD15 through proteolytic cleavage. This mechanism likely plays a crucial role in protecting the proper morphology of renal tubular structures and in cystogenesis in conjunction with PC1.
Our findings, which reveal altered mitochondrial ultrastructure and function in the Pkhd1 knockout kidney and cultured cells, indicate that FPC plays a critical role in regulating mitochondrial structure and function. Furthermore, our analysis of ICD15 in mitochondrial respiration provides compelling evidence that this cleavage product is involved in mediating the mitochondrial function of FPC. By targeting ICD15 to the mitochondria, it may participate in the regulation of essential mitochondrial processes, such as respiration and the production of critical metabolites involved in cell metabolism. Notably, our study revealed that ICD15 expression has a more pronounced effect on mitochondrial respiration in wild-type control mIMCD3 cells than in Pkhd1 KO cells. This observation suggests that the functional impact of ICD15 on mitochondria may be affected by the full-length FPC or other FPC cleavage products. These FPC forms contain the ciliary targeting sequence and may exert their function at primary cilia; the full-length FPC may mostly reside in the endoplasmic reticulum14. They may affect the responsiveness of mitochondria to ICD15, leading to a more specific effect of ICD15 on mitochondrial functions via unknown mechanisms. These observations suggest a complex interplay between FPC, ICD15, and mitochondrial function.
The genetic interaction between Pkhd1 KO or Pkhd1Δ3-4 allele and the Pkd1V allele leads to a phenotype similar to the Pkd1 null phenotype in the kidney and pancreas, two major organs affected in ADPKD. This finding suggests that FPC acts in conjunction with PC1, potentially by modulating the specific function of PC1 or interacting with downstream components of the PC1-specific pathway to maintain the proper morphology of renal tubular structures. A previous study found no evidence of physical interaction between full-length forms of FPC and polycystins in mouse kidneys45. However, a recent study identified a soluble C-terminal cleavage product of PC1 (CTT) that undergoes translocation to the mitochondria matrix36, impacting mitochondrial morphology, function, and cystogenesis36,37. It is plausible that FPC and PC1 may synergistically regulate a specific mitochondrial function through their respective cleavage products within mitochondria. It remains to be determined how their cleavage products are generated, and whether they physically interact with each other or with other molecules within mitochondria to regulate mitochondrial function.
The effects of Pkhd1 inactivation on mitochondrial structure and function observed in our study exhibit both similarities and differences when compared to a previous study conducted on PKHD1 mutant HEK293 cells39. While both studies observed cristae dilatation, there were discrepancies, such as larger mitochondria and increased OCR in the HEK293 cells. These differences may stem from variances in cell types, PKHD1/Pkhd1 mutations, and PC1 expression levels, underscoring the complex nature of FPC’s involvement in mitochondrial regulation.
One key finding highlighting the critical role of FPC in cystogenesis is the profound impact of Pkhd1Δ3-4/Δ3-4 or KO mutations on kidney and pancreas cystogenesis in hypomorphic Pkd1V/V mice, resulting in a phenotype similar to Pkd1 null. While PC1 has been established as a central player in cyst formation within the genetic interaction network for polycystic kidney and liver diseases44,53, the observed Pkd1 null-like phenotype in the digenic mutants cannot be explained by reduced levels or maturation of PC1V. Instead, our epistasis analysis using the Pkhd1Δ67/Δ67 and Pkd1V/V mutant strains suggests the involvement of the mitochondria-associated ICD15 specifically in the kidney cyst development. Interestingly, the presence of the Pkhd1Δ67/Δ67 mutation in Pkd1V/V mutants results in a less severe cystic phenotype. This observation could be attributed to the expression of FPC-ΔCT protein, which retains the intact ciliary targeting sequence and is likely directed to the cilia. This ciliary function may counteract renal cystogenesis through additional mechanisms involving its ecto- and transmembrane domains (See Fig. 7 for further discussion). In the pancreas, this ciliary function may be fully sufficient to protect the organ from cystogenesis through mechanisms beyond its C-terminal tail.
Previous studies have reported structural and functional alterations in mitochondria within the cystic kidney epithelia of Pkd1 mutants, with implications for modifying renal cyst growth31,32,36. However, the precise relationship between these mitochondrial alterations, polycystins, and their role in cystogenesis remains unclear. Our study reveals mitochondrial abnormalities in Pkhd1 KO kidney tubules despite the absence of cyst formation. Based on our findings, we propose that Pkhd1 inactivation creates a pro-cystic metabolic state due to the absence of FPC’s ICDs, which in turn exacerbates the Pkd1-dependent cystogenic pathway that is associated with the CTT of PC1. The combined effects contribute to the increased severity of the cystic phenotype in digenic mutants. Our findings suggest that ICD15 may serve as a crucial link to the Pkd1-dependent cystogenic pathway, implying that mitochondrial impairment may play a more proximate role in cystogenesis in the kidney. Future studies are necessary to determine the mechanisms by which dysfunctional C-terminal cleavage products of both FPC and PC1 within mitochondria lead to mitochondrial abnormalities involved in cystogenesis.
The importance of ICD products in the pathogenesis of ARPKD is underscored by the identification of truncating mutations and missense variants specifically situated in exon 67 of the PKHD1 gene in severe ARPKD patients58,59,60. For example, a frameshift mutation (V3925fs) combined with an F1785L mutation on the second allele was found in a severely affected ARPKD patient with enlarged cystic kidneys, chronic kidney disease, and portal hypertension59. The V3925fs frameshift mutation is predicted to result in the deletion of ICD15 by truncating FPC before the MTS. Another severely affected patient carried a variant P3968Lfs along with a C1431Y mutation on the second allele, resulting in truncation and loss of ICD12 due to disruption of the MTS cleavage site at P3968.
Our study suggests intriguing differences between human and mouse ICD15 in terms of mitochondrial import probability and accumulation, with human ICD15 displaying a higher import probability score and stronger mitochondrial accumulation than its mouse counterpart. These findings suggest that FPC, particularly through its ICD15 component, may exert a more significant role in mitochondrial function in humans, thereby implying that the loss of FPC in humans could have a more pronounced impact on mitochondrial function. This notion has important implications, especially considering the crucial involvement of mitochondrial disturbances in cyst formation during human fetal development. Evidence indicates that mutations in genes encoding mitochondrial proteins can independently result in cystogenesis in the kidneys of human fetuses61,62. Furthermore, human kidneys naturally have lower levels of functional PC1 due to abnormal alternative splicing of the PKD1 gene, resulting in premature termination of PC163. This intrinsic reduction in functional PC1, combined with the heightened impact of FPC on mitochondrial function, may contribute to the more severe pathology observed in ARPKD compared to mice.
Primary cilia play a role in inhibiting cyst formation in renal tubules but promote cyst growth in the absence of functional polycystins. Ma et al64 have proposed a cilia-dependent cyst activation (CDCA) signal that is activated to drive cystogenesis when polycystins are lost. Under normal conditions, polycystins are thought to tonically repress the CDCA signal, maintaining kidney homeostasis and facilitating tubular adaptation to environmental cues.
We propose a molecular mechanism to explain the interaction between Pkhd1 and Pkd1 in cystogenesis through a cilia-mitochondria connection (Fig. 7). According to our model, FPC present in primary cilia may act as a sensor for the extracellular environment and transmit information to mitochondria through the release of its ICD15 via proteolytic cleavage. When cilia lack functional PC1, a CDCA signal is generated and propagated to mitochondria, amplified by the absence of PC1’s CTT. FPC acts as a counterbalance to this signal both in cilia and through its mitochondrial ICD15 component. In Pkhd1 KO kidney, loss of FPC and its ICD15 alone has minimal effect on cystogenesis, at least in mice, due to the tonic suppression of CDCA by the presence of PC1. In Pkd1V/V kidney, PC1V’s impaired ciliary trafficking22,23 activates the CDCA signal, which may be further suppressed to some extent by PC1V outside the ciliary compartment. FPC’s ICDs further repress this signal within mitochondria, resulting in delayed and restricted renal cystogenesis24. In ΔCT/V kidney, the production of ICD15 is disrupted, preventing its ability to suppress the CDCA signal within mitochondria. However, FPC-ΔCT is still capable of localizing to the cilium and reducing CDCA levels. As a result, enhanced cystogenesis is observed compared to Pkd1V/V single mutants. In the Δ3–4/V and KO/V kidneys, the concurrent loss of FPC eliminates its regulatory influence on the CDCA signal, including its effect within the mitochondria. As a consequence, unopposed CDCA activity ensues, leading to severe cystogenesis that closely resembles the cystic phenotype observed in Pkd1 null mice. Further research is required to shed light on the specific molecular events and signaling pathways involved in the interplay between FPC and PC1 for the connection between cilia and mitochondria in polycystic kidney diseases.
Methods
Mice
Animal studies were performed in adherence to the NIH Guide for the Care and Use of Laboratory Animals and approved by the University of Maryland School of Medicine Institutional Animal Care and Use Committee (Protocol # 0421008). The mice were housed at a controlled temperature of 72 °F (±2 °F) with humidity maintained between 35% and 55%. They followed a 12-h light-dark cycle and had unrestricted access to LabDiet 5010-Laboratory Autoclavable Rodent Diet. Both male and female mice were used for experiments since phenotypes were consistent between the sexes. Littermates were compared when possible. All mice were congenic on a C57BL/6 J background. Embryos and neonates younger than 7 days of age were euthanized by decapitation using sharp scissors without prior sedation or anesthesia. Mice older than 7 days were euthanized using Isoflurane for anesthesia, followed by cervical dislocation to ensure euthanasia. Table 1 details the mice used in this investigation.
Antibodies
Homemade primary antibodies
Mouse FPC
We generated two new rat monoclonal antibodies, E3 and E4, directed to either side of the putative proprotein convertase site KRKR3613↓N in the extracellular region of mouse FPC11. E3 is directed to PECD N-terminal to the site (mouse FPC aa 3254-3353), while E4 is directed to PTM C-terminal to the position (mouse FPC aa 3610–3800). E1 is directed to the FPC C-terminus and has been previously described14. PC1: E8, a rat monoclonal antibody directed to CTF generated using a mouse polycystin-1 fragment (aa 3682–3882) as immunogen, has been previously described54. These antibodies are available through the Polycystic Kidney Disease Research Resource Consortium (https://www.pkd-rrc.org/fibrocystin-antibody/) and were used for immunoblotting at used at 1:500–1000 dilution.
Commercial primary antibodies
Mitochondria, Pyruvate Dehydrogenase (Abcam, 13G2AE2BH5; Immunoblot at 1 µg/ml); Aminopeptidase N (Abcam, ab108310; Immunoblot, 1:1000–10,000 dilution); THP, Tamm-Horsfall glycoprotein/Uromodulin (Santa Cruz, sc-20631; Immunoblot, 1:1000 dilution); Aquaporin2, AQP2, (Sigma, A7310; Immunoblot, 1:200–1:1000 dilution); β-Actin (Sigma, A5441; Immunoblot, 1:5000–10,000 dilution); E-cadherin, E-Cad (Cell Signaling, 3195 P; Immunoblot, 1:1000 dilution); TOM20 (Cell Signaling, 42406 T; Immunoblot, 1:500–1000 dilution), Tubulin (Sigma, T6793; Immunoblot, 1:2000 dilution), Actin-Rhodamine (BioRad, 12004163; Immunoblot, 1:1000–10,000 dilution).
Secondary antibodies
Goat anti-Rat HRP (Sigma, NA935V); Alexa Fluor donkey anti-mouse 555 (Invitrogen, A31570); Alexa Fluor donkey anti-rabbit 647 (Invitrogen, A31573).
Western blot
Cells and kidneys were lysed in either 1% Triton lysis buffer or RIPA buffer with Complete protease inhibitor cocktail added (Roche, 11697498001). Lysates were loaded on 4–12% Bis-Tris protein gels (Invitrogen, NP0336BOX) and run with MES running buffer (Invitrogen, NP0002). Proteins were transferred to polyvinylidene fluoride (PVDF) membranes, blocked with 5% non-fat milk block for 30 min, and incubated with primary antibodies at 4 °C overnight. Membranes were washed with Tris-buffered saline containing Tween (TBST) and probed with fluorescent- or horseradish peroxidase (HRP)-conjugated secondary antibodies prior to detection using either a BioRad ChemiDoc Imaging System or radiographic film.
Immunohistochemistry
Tissues were harvested, fixed with 4% paraformaldehyde (PFA), and embedded in paraffin before being sectioned, and stained with hematoxylin and eosin using standard protocols. Lectin staining was carried out on 5 µm paraffin sections. After deparaffinization with xylenes, sections were rehydrated in an ethanol series before boiling in citrate buffer (DAKO Cytomation, S2369) for antigen retrieval. After blocking, sections were incubated with Lotus Tetragonolobus Lectin (LTL)-Fluorescein (Vector Laboratories, FL-1321; used at 2 mg active conjugate/ml) and Dolichos Biflorus Agglutinin (DBA)-Rhodamine (Vector Laboratories, RL-1032; used at 2 mg active conjugate/ml), for 1 h. After PBS washes, sections were incubated with DAPI, PBS washed, and mounted with Fluoromount-G (Invitrogen, 00-4958-02).
Cell culture, transfection, and immunofluorescence
mIMCD3 (ATCC; CRL-2123), MDCK23 and HEK293 (ATCC, CRL-1573) cells were cultured in DMEM/F12 medium with GlutaMAX (Thermo Fisher Scientific, #31331093), supplemented with 10% FBS, 1% Penicillin-Streptomycin (PenStrep) (Thermo Fisher Scientific, #15070-063) and 1% Sodium Pyruvate (Thermo Fisher Scientific, #11360-039). Transfection was performed using standard lipofectamine2000 (Invitrogen, 11668019) transfection protocols and as previously described23. Fluorescent images were obtained using Zeiss Axio Observer D1 microscope and the associated software ZEN (blue edition).
Split GFP complementation assay
For the split GFP complementation assay and ICD15-GFP localization, mIMCD3 cells were co-transfected with complementary constructs or single construct controls and plated on coverslips in 6-well plates. Growth medium was replaced after 24 h, and cells were allowed to recover for 24 h before fixation with room temperature 4% PFA (10 min). Fixed cells were permeabilized with 0.25% Triton (3 min) and stained with DAPI before mounting with Fluoromount-G (Invitrogen 00-4958-02). For the split GFP assay48, three separate experiments per construct were imaged 24–48 h after transfection. All constructs were co-transfected with mts-mCherry-GFP1-10. Therefore, mitochondria were labeled with mCherry.
Cellular fractionation
A serial centrifugation protocol was used to enrich for mitochondria65. Briefly, MDCK cell lines stably expressing FPC constructs were scraped in phosphate-buffered saline (PBS) and pelleted by centrifugation. After resuspension in STE medium (250 mM sucrose, 5 mM Tris, 2 mM EGTA; pH 7.4 at 4 °C), cells were homogenized using a Dounce homogenizer. Mitochondria were isolated by differential centrifugation. The final mitochondrial fraction was collected and resuspended in a minimal volume of STE.
CRISPR/Cas9 generation of Pkhd1 KO mIMCD3
To generate Pkhd1 KO mIMCD3, U6gRNA-Cas9-2A-GFP plasmids (Sigma-Aldrich) carrying three distinct custom-designed guide RNA (gRNA) sequences targeting exons 4, 16 and 18 were used (gRNA#1: GACGTCTCTCCGGCCTTCG; gRNA#2: TTGACTCTTGGGAGCAGAT; gRNA#3: TGCAATCTGGCACCGTTTT). The most efficient guides (gRNA#1 and #2) were employed. Cells were plated on 150 mm2 plates the day before the transfection. Transfection was performed using Lipofectamine 3000 (Thermo Fisher Scientific, #L3000015) following the manufacturer’s instructions. 5 μg of plasmid DNA per dish with 1:3 DNA/Lipofectamine ratio were used. The CMV-Cas9-2A-RFP scrambled gRNA was used as a control. Three days after transfection cells were sorted by FACS for GFP (potential Pkhd1 KO mIMCD3) or RFP (control mIMCD3) and plated as single cells into 96-wells plates. The vital clones were sequentially expanded and screened for FPC protein expression by western blot. Four out of nine Pkhd1 KO clones were established by guides #1 or #2. As controls, nine RFP clones were generated (Cassina and Boletta, in preparation). The guide RNA sequence targeting exon 2 of murine Pkhd1 sequence (gRNA#4: 5′-ACTCCCTGGAAATGCGCTCTGG-3′) was also successfully used in the system.
Seahorse metabolic flux analysis
The day before the assay, 15,000 cells per well in 96-well Seahorse cell culture and incubated in a 5% CO2 incubator at 37 °C overnight. The day after the culture medium was changed with Seahorse XF DMEM medium (Agilent Technologies, #103575-100) supplemented with 10 mM glucose, 1 mM sodium pyruvate, and 2 mM L-glutamine. The plate was incubated at 37 °C for 1 h in a non-CO2 incubator before starting the assay. We performed Mito Stress Test assay. After OCR baseline measurements oligomycin A (O), carbonyl cyanide 4-(trifluoromethoxy) phenylhydrazone (FCCP), and antimycin A/rotenone (A/R) were added sequentially to each well, to reach the final concentrations of 1 μM O, 1.5 μM FCCP, and 0.5 μM A/R. Results were normalized by cell number using CyQUANT Cell Proliferation Assays (Thermo Fisher Scientific, #C35011). Results are mean ± SD of technical replicates, OCR data are expressed as pmol of oxygen per minute per arbitrary units (pmol/min/a.u.). All the analyses were performed with the Agilent Seahorse Wave software (Agilent). Basal respiration was calculated by subtracting the minimum OCR measurement after A/R injection from the last OCR measurement before oligomycin injection, maximal respiration by subtracting the last OCR measurement before oligomycin injection from the maximum rate measured after FCCP injection, spare respiratory capacity by subtracting the basal respiration from the maximal respiration.
N-glycosylation analysis
Samples were denatured using glycoprotein denature buffer (New England Biolabs) for 1 min at 95 °C and then quickly chilled on ice. The denatured glycoprotein was incubated with PNGaseF or EndoH (New England Biolabs) for 1 h at 37 °C.
Kidney dissection and tubules isolation
Kidneys were harvested under sterile conditions from P6 WT and Pkhd1 null mice, followed by mincing the kidneys into 1 mm3 cubes and incubating in collagenase II digestion (0.1 g/ml, Sigma C2139) solution at 37 °C with shaking for 30 mins. Tubule cells were collected by centrifugation and resuspended in DMEM/F12 containing DNase I (2U/ml, Sigma D4263). After 3 mins of DNase I digestion, tubule cells were collected by centrifugation and the resuspended pellet was filtered through 70 µm pore filters to isolate tubules and exclude glomeruli. The tubules were washed in ice-cold PBS and pulsed in a centrifuge three times to remove collagenase and red blood cells. After each spin, the pellets become increasingly opaque white. The remaining pellets are isolated kidney tubule fragments.
Transmission electron microscopy
P6 kidneys were collected and fixed using TEM fixative (2% Paraformaldehyde, 2.5% Glutaraldehyde, 2 mM CaCl2 in 0.1 M PIPES buffer, pH 7.35) and postfixed with reduced osmium. Fixed specimens were washed with buffer, dehydrated in a graded series of ethanols, embedded in plastic resin, and cut to 80–100 nm sections by Leica UC6 ultramicrotome. The sections were stained with uranyl acetate and Sato’s triple lead stain, and images were collected of whole tubules, followed by higher magnification images of individual cells and mitochondria by transmission electron microscope FEI tecnai T12 at the Electron Microscopy Core Imaging Facility of the University of Maryland Baltimore.
Analysis and Statistics
Mitochondrial localization signal prediction was undertaken using Mitoprot II46 (https://ihg.helmholtz-muenchen.de/ihg/mitoprot.html). Mitochondria shape descriptors were calculated using ImageJ software (http://rsb.info.nih.gov/ij/) (version 1.54 f). Averages are represented in graphs with SEM error bars. Images were blinded to genotype and processed for shape descriptor analysis and cristae diameter measurements. Data analysis was undertaken using Microsoft Excel (office 365), R studio (version 1.4.1106) (https://www.rstudio.com/).
Cystic area calculation
Images of sections of P0 kidneys were analyzed using ImageJ software. Kidney slices were binarized, and cyst areas were measured using “analyze particles”. All fenestrations >10 µm diameter were counted. The “cyst” areas were compared with the area of the kidney slice to produce a % cystic area.
Reporting summary
Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.
Data availability
All data generated or analyzed during this study are included in this article (and its supplementary information files). Source data are provided with this paper.
References
Harris, P. C. & Torres, V. E. Polycystic kidney disease. Annu Rev. Med 60, 321–337 (2009).
Igarashi, P. & Somlo, S. Genetics and pathogenesis of polycystic kidney disease. J. Am. Soc. Nephrol. 13, 2384–2398 (2002).
Guay-Woodford, L. M. Autosomal recessive polycystic kidney disease: the prototype of the hepato-renal fibrocystic diseases. J. Pediatr. Genet. 3, 89–101 (2014).
Hartung, E. A. & Guay-Woodford, L. M. Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects. Pediatrics 134, e833–e845 (2014).
Nakanishi, K., Sweeney, W. E. Jr., Zerres, K., Guay-Woodford, L. M. & Avner, E. D. Proximal tubular cysts in fetal human autosomal recessive polycystic kidney disease. J. Am. Soc. Nephrol. 11, 760–763 (2000).
Ward, C. J. et al. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein. Nat. Genet. 30, 259–269 (2002).
Onuchic, L. F. et al. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats. Am. J. Hum. Genet 70, 1305–1317 (2002).
Lu, H. et al. Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease. Nat. Genet. 49, 1025–1034 (2017).
Follit, J. A., Li, L., Vucica, Y. & Pazour, G. J. The cytoplasmic tail of fibrocystin contains a ciliary targeting sequence. J. Cell Biol. 188, 21–28 (2010).
Hiesberger, T. et al. Proteolytic cleavage and nuclear translocation of fibrocystin is regulated by intracellular Ca2+ and activation of protein kinase C. J. Biol. Chem. 281, 34357–34364 (2006).
Kaimori, J. Y. et al. Polyductin undergoes notch-like processing and regulated release from primary cilia. Hum. Mol. Genet. 16, 942–956 (2007).
Menezes, L. F. et al. Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm. Kidney Int. 66, 1345–1355 (2004).
Ward, C. J. et al. Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia. Hum. Mol. Genet. 12, 2703–2710 (2003).
Outeda, P. et al. A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanism. Kidney Int. 92, 1130–1144 (2017).
Gallagher, A. R. et al. Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1. Am. J. Pathol. 172, 417–429 (2008).
Wang, S., Luo, Y., Wilson, P. D., Witman, G. B. & Zhou, J. The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area. J. Am. Soc. Nephrol. 15, 592–602 (2004).
Bakeberg, J. L. et al. Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystin. J. Am. Soc. Nephrol. 22, 2266–2277 (2011).
Gabow, P. A. Autosomal dominant polycystic kidney disease. N. Engl. J. Med 329, 332–342 (1993).
Boletta, A. & Germino, G. G. Role of polycystins in renal tubulogenesis. Trends Cell Biol. 13, 484–492 (2003).
Lu, W. et al. Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation. Nat. Genet. 17, 179–181 (1997).
Piontek, K. B. et al. A functional floxed allele of Pkd1 that can be conditionally inactivated in vivo. J. Am. Soc. Nephrol. 15, 3035–3043 (2004).
Kim, H. et al. Ciliary membrane proteins traffic through the Golgi via a Rabep1/GGA1/Arl3-dependent mechanism. Nat. Commun. 5, 5482 (2014).
Qian, F. et al. Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations. Proc. Natl Acad. Sci. USA 99, 16981–16986 (2002).
Yu, S. et al. Essential role of cleavage of Polycystin-1 at G protein-coupled receptor proteolytic site for kidney tubular structure. Proc. Natl Acad. Sci. USA 104, 18688–18693 (2007).
Ha K., et al. The heteromeric PC-1/PC-2 polycystin complex is activated by the PC-1 N-terminus. Elife https://doi.org/10.7554/eLife.60684, 1-23 (2020).
Wang, Z. et al. The ion channel function of polycystin-1 in the polycystin-1/polycystin-2 complex. EMBO Rep. 20, e48336 (2019).
Mishra, P. & Chan, D. C. Metabolic regulation of mitochondrial dynamics. J. Cell Biol. 212, 379–387 (2016).
Varanita, T. et al. The OPA1-dependent mitochondrial cristae remodeling pathway controls atrophic, apoptotic, and ischemic tissue damage. Cell Metab. 21, 834–844 (2015).
Rowe, I. et al. Defective glucose metabolism in polycystic kidney disease identifies a new therapeutic strategy. Nat. Med. 19, 488–493 (2013).
Menezes, L. F., Lin, C. C., Zhou, F. & Germino, G. G. Fatty acid oxidation is impaired in an orthologous mouse model of autosomal dominant polycystic kidney disease. EBioMedicine 5, 183–192 (2016).
Cassina, L., Chiaravalli, M. & Boletta, A. Increased mitochondrial fragmentation in polycystic kidney disease acts as a modifier of disease progression. FASEB J. 34, 6493–6507 (2020).
Ishimoto Y., et al. Mitochondrial abnormality facilitates cyst formation in autosomal dominant polycystic kidney disease. Mol. Cell Biol. 37, 24 (2017).
Padovano, V. et al. The polycystins are modulated by cellular oxygen-sensing pathways and regulate mitochondrial function. Mol. Biol. Cell 28, 261–269 (2017).
Hofherr, A. et al. The mitochondrial transporter SLC25A25 links ciliary TRPP2 signaling and cellular metabolism. PLoS Biol. 16, e2005651 (2018).
Kuo I. Y., et al. Polycystin 2 regulates mitochondrial Ca(2+) signaling, bioenergetics, and dynamics through mitofusin 2. Sci. Signal 12, 580 (2019).
Lin, C. C. et al. A cleavage product of Polycystin-1 is a mitochondrial matrix protein that affects mitochondria morphology and function when heterologously expressed. Sci. Rep. 8, 2743 (2018).
Onuchic, L. et al. The C-terminal tail of polycystin-1 suppresses cystic disease in a mitochondrial enzyme-dependent fashion. Nat. Commun. 14, 1790 (2023).
Hajarnis, S. et al. microRNA-17 family promotes polycystic kidney disease progression through modulation of mitochondrial metabolism. Nat. Commun. 8, 14395 (2017).
Chumley, P. et al. Truncating PKHD1 and PKD2 mutations alter energy metabolism. Am. J. Physiol. Ren. Physiol. 316, F414–F425 (2019).
Williams, S. S., Cobo-Stark, P., James, L. R., Somlo, S. & Igarashi, P. Kidney cysts, pancreatic cysts, and biliary disease in a mouse model of autosomal recessive polycystic kidney disease. Pediatr. Nephrol. 23, 733–741 (2008).
Woollard, J. R. et al. A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation. Kidney Int. 72, 328–336 (2007).
Moser, M. et al. A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD). Hepatol. 41, 1113–1121 (2005).
Garcia-Gonzalez, M. A. et al. Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway. Hum. Mol. Genet. 16, 1940–1950 (2007).
Fedeles, S. V. et al. A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation. Nat. Genet. 43, 639–647 (2011).
Olson, R. J. et al. Synergistic genetic interactions between Pkhd1 and Pkd1 Result in an ARPKD-Like phenotype in murine models. J. Am. Soc. Nephrol. 30, 2113–2127 (2019).
Claros, M. G. & Vincens, P. Computational method to predict mitochondrially imported proteins and their targeting sequences. Eur. J. Biochem. 241, 779–786 (1996).
Bolender, N., Sickmann, A., Wagner, R., Meisinger, C. & Pfanner, N. Multiple pathways for sorting mitochondrial precursor proteins. EMBO Rep. 9, 42–49 (2008).
Ruan, L. et al. Cytosolic proteostasis through importing of misfolded proteins into mitochondria. Nature 543, 443–446 (2017).
Woodard, L. E. & Wilson, M. H. piggyBac-ing models and new therapeutic strategies. Trends Biotechnol. 33, 525–533 (2015).
Bhargava, P. & Schnellmann, R. G. Mitochondrial energetics in the kidney. Nat. Rev. Nephrol. 13, 629–646 (2017).
Lam J., et al. A universal approach to analyzing transmission electron microscopy with imageJ. Cells 10, 2177 (2021).
Ahrabi, A. K. et al. Glomerular and proximal tubule cysts as early manifestations of Pkd1 deletion. Nephrol. Dial. Transpl. 25, 1067–1078 (2010).
Fedeles, S. V., Gallagher, A. R. & Somlo, S. Polycystin-1: a master regulator of intersecting cystic pathways. Trends Mol. Med. 20, 251–260 (2014).
Kurbegovic, A. et al. Novel functional complexity of polycystin-1 by GPS cleavage in vivo: role in polycystic kidney disease. Mol. Cell Biol. 34, 3341–3353 (2014).
Pema, M. et al. mTORC1-mediated inhibition of polycystin-1 expression drives renal cyst formation in tuberous sclerosis complex. Nat. Commun. 7, 10786 (2016).
Walker R., Xu, H., Huang, Q., Qian, F. in Polycystic Kidney Disease (eds. Hu J., Yu, & Yong) 23 (CRC Press, 2019).
Raynaud, P. et al. A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis. Hepatol. 53, 1959–1966 (2011).
Gunay-Aygun, M. et al. PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis. Mol. Genet. Metab. 99, 160–173 (2010).
Dafinger, C. et al. The carboxy-terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC-activation. J. Cell Mol. Med. 24, 14633–14638 (2020).
Fokkema, I. F. et al. LOVD v.2.0: the next generation in gene variant databases. Hum. Mutat. 32, 557–563 (2011).
Podrini, C., Cassina, L. & Boletta, A. Metabolic reprogramming and the role of mitochondria in polycystic kidney disease. Cell Sig. 67, 109495 (2020).
Hackl, A. et al. Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities. Pediatr. Nephrol. 32, 791–800 (2017).
Lea, W. A. et al. Human-specific abnormal alternative splicing of wild-type PKD1 induces premature termination of polycystin-1. J. Am. Soc. Nephrol. 29, 2482–2492 (2018).
Ma, M., Tian, X., Igarashi, P., Pazour, G. J. & Somlo, S. Loss of cilia suppresses cyst growth in genetic models of autosomal dominant polycystic kidney disease. Nat. Genet. 45, 1004–1012 (2013).
Jastroch, M., Hirschberg, V. & Klingenspor, M. Functional characterization of UCP1 in mammalian HEK293 cells excludes mitochondrial uncoupling artefacts and reveals no contribution to basal proton leak. Biochim. Biophys. Acta. 1817, 1660–1670 (2012).
Parnell, S. C. et al. A mutation affecting polycystin-1 mediated heterotrimeric G-protein signaling causes PKD. Hum. Mol. Genet. 27, 3313–3324 (2018).
Acknowledgements
This work was supported by National Institute of Health (NIH) grants R01 DK111611 and R01 DK125404 (FQ), Polycystic Kidney Disease Foundation grant 236G19a (FQ), the University of Maryland Baltimore Institute for Clinical & Translational Research grant (Project ID 14) (FQ), a Polycystic Kidney Disease Foundation fellowship grant (215F19a) (RW) and by funds from the Italian Association for Research on PKD (A.B.). We also acknowledge the Polycystic Kidney Disease Research Resource Consortium (U54DK126114) for providing us with the E1, E3, and E4 antibodies used in this study. We thank Gianfranco Distefano for technical help with the generation of mIMCD3 cells KO for Pkhd1. We thank Gary Fiskum for his critical reading of the manuscript and helpful discussions, and Ru-Ching Hsia and Christine Brantner for assistance in transmission electron microscopy.
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F.Q., R.V.W. and Q.Y. developed the concept of this study. R.V.W., H.X., Q.Y., A.M., B.M.P., K.F.S., S.R., R.L., L.C., A.B. and F.Q. designed and performed experiments, and analyzed data. P.O. and T.W. provided reagents. R.V.W. and F.Q. prepared the draft and final version of the manuscript. All authors read and approved the final manuscript.
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Walker, R.V., Yao, Q., Xu, H. et al. Fibrocystin/Polyductin releases a C-terminal fragment that translocates into mitochondria and suppresses cystogenesis. Nat Commun 14, 6513 (2023). https://doi.org/10.1038/s41467-023-42196-4
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DOI: https://doi.org/10.1038/s41467-023-42196-4
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