Exosome miR-371b-5p promotes proliferation of lung alveolar progenitor type II cells by using PTEN to orchestrate the PI3K/Akt signaling
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Pathways directing endogenous stem/progenitor cells to restore normal architecture and function of damaged/diseased lungs remain underexplored. Published data have revealed that alveolar progenitor type II cell (ATIIC)-derived signaling promotes re-epithelialization of injured alveoli, yet the underlying mechanism is unknown. Here we aim to define the role of ATIIC-derived exosome miRNA signaling in controlling ATIIC-specific proliferation or differentiation in response to injury.
Pluripotent stem cell-derived cultures, which contain early lung stem/progenitor populations that can subsequently differentiate into ATIICs, were used as a model for unbiased screening and identification of ATIIC phenotype-specific exosome miRNA signaling, and human induced pluripotent stem cell-derived ATIICs (hiPSC-ATIICs) were employed to examine the molecular basis of key exosome miRNA signaling in promoting ATIIC-specific proliferation. QRT-PCR was performed to examine expression pattern of ATIIC-derived key exosome miRNA in an alveolar injury model and in injured human lungs.
We show that human ATIIC line (A549)-derived exosome miR-371b-5p promotes ATIIC-specific proliferation, but not differentiation, in differentiating cultures of pluripotent stem cells. Using 3′UTR-driven luciferase reporters, we identified PTEN as a direct target of miR-371b-5p. Transfection of miR-371b-5p mimic into hiPSC-ATIICs leads to significantly decreased expression of endogenous PTEN, which stimulates phosphorylation of Akt and its downstream substrates, GSK3β and FOXOs, promoting cell proliferation. While not expressed in normal ATIIC phenotypes, the exosome miR-371b-5p expression is significantly induced after hiPSC-ATIICs or hATIICs (human primary ATIICs) are subjected to bleomycin-induced injury. To rule out that the ATIIC-derived exosome-miRNAs are merely a cell culture phenomenon, we transplanted hiPSC-ATIICs into bleomycin-challenged lungs of mice, and found that the transplanted hiPSC-ATIICs engraft and express exosome miR-371b-5p, along with additional survival of numerous mouse ATIICs in bleomycin-injured lungs. Consistent with these findings, significant levels of exosome miR-371b-5p were also detected in lavage samples of patients with acute pneumonia, but not in those from patients without pulmonary disorders.
Collectively, our data strongly suggest that ATIIC-derived exosome miR-371b-5p may serve as a niche signaling to augment ATIIC survival/proliferation, promoting re-epithelialization of injured alveoli, and thus provide a promising novel target to develop treatment for currently incurable lung diseases.
KeywordsExosome miRNAs MiR-371b-5p PTEN/PI3K/Akt signaling Lung alveolar progenitor type II cells Lung injury
Alveolar epithelial type I cells
Alveolar epithelial type II cells
human primary ATIICs
Human embryonic stem cells
Human induced pluripotent stem cell-derived ATIICs
Human peripheral blood monocytes
mouse primary ATIICs
Surfactant protein C
SPC promoter/neomycinR transgene
Alveolar epithelial type II cells (ATIICs) serve as alveolar progenitor critical for maintaining the integrity of alveolar epithelium, a structure essential for O2/CO2 exchange. Failure to repair injured alveolar epithelium has been implicated in the development of many life-threatening pulmonary diseases, including acute respiratory distress syndrome, chronic obstructive pulmonary disease, and pulmonary fibrosis. Crosstalk between ATIICs and mesenchymal cells is thought to play an important role in distal lung development, yet niche signaling supporting ATIIC function in response to injury remains largely unknown. We have observed in our previous studies that transplanted ATIICs derived from human pluripotent stem cells not only engraft and differentiate into alveolar epithelial type I cells (ATICs) for repair of injured mouse alveoli, but also provide an appropriate signal microenvironment to promote the repair capacity of endogenous ATIICs [1, 2], suggesting a pivotal role of signal communication between ATIICs or between ATIICs and their upstream stem cells in controlling ATIIC-specific proliferation or differentiation in response to injury.
Exosomes are cell-derived extracellular vesicles containing functional proteins, mRNAs and microRNAs (miRNAs), and serve as a key mediator in intercellular communication [3, 4, 5]. Distinct miRNA expression patterns have been found in different tissues, cell types, and developmental stages , and shown to play a critical role in controlling various cellular processes such as stem cell self-renewal, proliferation, differentiation, and tissue development [7, 8, 9, 10, 11, 12, 13, 14, 15, 16]. Hence, exosomes are likely to be an efficient and robust means to transfer miRNAs and regulate physiological functions of neighboring and distant tissue progenitor cells for tissue regeneration. Because secreting and recycling of vesicle-rich surfactant by ATIICs is a key process in surfactant metabolism in lung , we hypothesize that ATIIC-derived exosome miRNAs (Exo-miRs) may be critical to carry cell-to-cell communication necessary for maintaining alveolar homeostasis in response to injury.
MiRNAs, on average 22 nucleotide long, endogenous non-coding RNA molecules, suppress gene expression post-transcriptionally by binding to partially complementary sites within 3′UTR regions of mRNAs in all eukaryotic cells. Over 1000 miRNAs have been identified in human , which may target about 60% mammalian genes [19, 20]. Despite mounting evidence demonstrating their importance in numerous cellular processes, little is known about the role of Exo-miR-mediated cellular communications in lung physiology. We here report that a human ATIIC line, A549, expresses exosome miR-371b-5p, which promotes ATIIC-specific proliferation by orchestrating PTEN/PI3K/AKT signaling pathway. While human induced pluripotent stem cell-derived ATIICs (hiPSC-ATIICs) and human primary ATIICs (hATIICs) do not express exosome miR-371b-5p, exosomes isolated from bleomycin (BLM)-treated hiPSC-ATIICs and hATIICs express a significant level of miR-371b-5p. Consistently, lung lavage exosomes of patients with acute pneumonia, but not those without any pulmonary disorders, express miR-371b-5p. In further exploration of the possibility of ATIIC-derived exosome miR-371b-5p serving as a niche signaling, we show the capacity of transplanted hiPSC-ATIICs to engraft and secrete exosome miR-371b-5p in response to injury, along with additional survival of numerous mouse ATIICs in the BLM-injured lungs. These results suggest an essential role of exosome miR-371b-5p-mediated communication between ATIICs in response to lung injury, and that exosome miR-371b-5p may represent a novel therapeutic target for repair of injured alveoli.
A hiPSC line, hiPSC-26B  was cultured on Matrigel-coated plates in differentiation medium (DM) containing 20% FBS (HyClone, Logan, UT, USA), 1% nonessential amino acid, 1 mM L-glutamine, 100 μg/ml penicillin, 100 μg/ml streptomycin, and 20 μg/ml G418 in Knockout DMEM (Gibco, Invitrogen, Waltham, MA, USA) for 14 days, which allows us to select a pure population of functional ATIICs. The hATIICs and mATIICs (mouse primary ATIICs) were prepared as previously described [21, 22]. Human peripheral blood monocytes (hmonos) and NK cells were isolated from peripheral blood samples (Gulf Coast Regional Blood Center, Houston, TX, USA) by using the density gradient centrifugation (Ficoll-Paque) and the NK Cell Isolation Kit (MACS; Miltenyi Biotec, Bergisch Gladbach, Germany), respectively, as previously reported .
Preparation of ATIIC phenotype-derived exosomes and Exo-miRs
A549 cells, hiPSC-ATIICs, and hATIICs were cultured on Matrigel-coated plates with exosome-depleted DM. The medium was collected from each phenotype [A549-, hiPSC-ATIIC-, and hATIIC-conditioned DM or conditioned medium (CM)] in 24 hours, from which exosomes were then isolated using ExoQuick-TC Exosome Precipitation Solution (System Biosciences, Palo Alto, CA, USA) for small RNA (<200 nt) preparation using the mirVana™ miR Isolation kit (Ambion, Austin, TX, USA) by following the manufacturer’s instructions. To prepare exosomes and Exo-miRs from injured ATIICs, we established an ATIC/ATIIC co-culture model. Briefly, 5 × 105 hiPSC-ATIICs were placed in the lower chamber of each six-well transwell plate with DMEM containing 10% FBS and left to spontaneously differentiate for 8 days [1, 2], which allows 100% placed hiPSC-ATIICs to differentiate into ATICs (hiPSC-ATICs) expressing AQP5 and T1α as shown in Additional file 1: Figure S2. Then the derived ATICs were switched to exosome-depleted DM, and 1 × 106 freshly isolated hiPSC-ATIICs or hATIICs were placed in each transwell insert (Matrigel-coated, 0.4 mm pores) with 1 ml exosome-depleted DM. Next day, various doses (10, 20, 30, and 40 μg/ml) of BLM were added to the medium to induce injury for 24 hours before exosome and Exo-miR isolation.
Exosome miRNA profiling analysis
Exo-miRs were prepared for array analysis (performed by LC Sciences, Houston, TX, USA). The human miRNA array (MRA-1001) that targets all known human mature miRNAs in the miRNA database (Release 18, hrrp://microrna.sanger.ac.uk) was used. The miRNA expression levels identified in the analyses were validated by QRT-PCR for consistency.
Construction of miRNA-inhibitor vectors
For each miRNA-inhibitor vector, a double-stranded oligonucleotide was designed to contain a targeting motif for specific binding to an individually selected miRNA molecule, with Xho I or Xba I overhang at each end, and was then cloned into Sal I and Xba I sites downstream of the U6 promoter in the pSuppressorNeo vector as shown in Fig. 2c. The sequences of targeting motifs are listed in the figure legends.
Examination of the effect of ATIIC-derived signaling on ATIIC-specific differentiation or proliferation
To examine the effect of ATIIC phenotype-derived signaling on ATIIC-specific differentiation or proliferation in the cultures of pluripotent stem cells, a human embryonic stem cell (hESC) line, SPCP/NEO74 , which harbor ATIIC-specific surfactant protein C (SPC) promoter/neomycinR (SPCP/NEOR) transgene, was cultured on Matrigel-coated six-well plates in DM for 6 days, and then some of the differentiating cultures were switched to A549-CM, hiPSC-ATIIC-CM, hATIIC-CM, or DM containing ATIIC phenotype-derived exosomes for 6 or 10 days, with the medium changed every day. Exosomes isolated from 5 × 106 each ATIIC phenotype were added into one corresponding well for the study. In order to test the effect of A549-derived Exo-miRs on ATIIC-specific proliferation, the hESC-derived cultures were co-transfected with A549-derived Exo-miRs (1.0 μg) and one selected individual miRNA inhibitor vector (0.5 μg) on days 6 and 12 using Lipofectamine® RNAiMAX Transfection Reagent (Invitrogen). To determine the content of the derived SPC-expressing cells in the differentiated cultures of hESCs, the differentiated cells were stained with 1:500 diluted anti-human proSPC antibody (Chemicon, Temecula, CA, USA) on days 12 and 16. The number of SPC-positive cells was counted per 1000 cells based on 4′,6-diamidino-2-phenylindole (DAPI, Biostatus, Loughborough, UK) staining on each plate. To examine the capacity of miR-371b-5p to induce ATIIC proliferation, the G418-selected hiPSC-ATIICs in six-well plates were transfected with various doses (50, 100, and 150 pmols/well) of miR-371b-5p mimic (Ambion) and then incubated with 10 μM bromodeoxyuridine (BrdU) (Abcam, Cambridge, MA, USA) for 12 hours to label the proliferating cells. Proliferation was assessed 2 days after transfection using the CellTiter 96®AQueous One Solution Cell Proliferation Assay Kit (Promega, Madison, WI, USA).
Immunofluorescent staining and Western blot analysis
Differentiated hESCs and hiPSC-ATIICs were washed twice with PBS and fixed in 4% paraformaldehyde for 15 minutes. Washed cells were permeabilized in 0.5% Triton X (Sigma-Aldrich, St. Louis, MO, USA) for 30 minutes before being blocked in 5% goat serum for 2 hours. Cells were then stained with 1:500 diluted rabbit anti-human proSPC antibody and/or mouse anti-BrdU antibody (1:100, Abcam), and visualized with Alexa Fluor 546- or 488-conjugated goat anti-rabbit IgG or Alexa Fluor 546-conjugated goat anti-mouse IgG (1:1000, Molecular Probes, Eugene, OR, USA) with 1:1000 diluted DAPI counterstaining. In addition, the rabbit anti-human proSPC and mouse anti-human nuclei monoclonal antibody (Chemicon) were used for immunofluorescent staining of tissue sections of BLM-challenged lungs transplanted with hiPSC-ATIICs as previously reported [1, 2]. For Western blot analysis, protein extracts (20 μg) from miR-371b-5p mimic-treated hiPSC-ATIICs were prepared. Rabbit anti-human Akt/pAkt, Erk/pErk, GSK3β/pGSK3β, FOXO3/pFOXO3, FOXO1/pFOXO1, PTEN, and GAPDH (Cell Signaling, Danvers, MA, USA) were used in the study. In addition, 10 μg ATIIC phenotype-derived exosomal proteins were analyzed for exosome marker expression by using rabbit anti-TSG101, mouse anti-CD63 and mouse anti-HSP70 antibody (Abcam).
Dual-luciferase miRNA target reporter assay
To generate the dual-luciferase miRNA target reporter vector, a double-stranded oligonucleotide containing wild-type (wt) PTEN 3′UTR sequence with a predicted miR-371b-5p target site or mutant PTEN 3′UTR sequence was cloned into Pmel and XbaI sites in pmirGLO Dual-Luciferase miRNA Target Expression Vector (Promega, Fig. 4b). The hiPSC-ATIICs of 70% confluence in 24-well plates were co-transfected with the dual-luciferase miRNA target reporter vector (0.3 μg) and miR-371b-5p mimic (15 pmol/well). Cell extracts were prepared 24 hours after transfection, and the luciferase activity was measured using the Dual-Luciferase Reporter Assay System (Promega).
0.5 μg total cellular/exosome RNA (0.1 μg for human/mouse lavage exosome RNA) were prepared for QRT-PCR analysis using TaqMan One-Step RT-PCR Master Mix Kit (AB Applied Biosystems, Foster City, CA, USA) as previously described , using the following primers and probes: (1) miR-371b-5p primers (ABM Inc., Richmond, BC, Canada); (2) SPC forward primer (5′-GTC CTC ATC GTC GTG GTG ATT-3′), SPC reverse primer (5′-CGT GTG TTT CTG GCT CAT GTG -3′), and SPC probe (5′- 6-FAM-AGA CCC ATG AGC AGG GCT CCC -TAMRA-3′); (3) PTEN forward primer (5′- ACC CAC ACG ACG GGA AGA CA -3′), PTEN reverse primer (5′- CTG TTT GTG GAA GAA CTC TAC TTT GAT ATC AC -3′), and PTEN probe (5′-6-FAM-CAT GTA CTT TGA GTT CCC TCA GCC GTT ACC TGT G-TAMRA-3′); and (4) 18S forward primer (5′-TAA CGA ACG AGA CTCTGG CAT-3′), 18S reverse primer (5′-CGG ACA TCT AAG GGC ATC ACA G-3′), and 18S probe (5′-FAM-TGG CTG AAC GCC ACT TGT CCC TCT AA-TAMRA-3′).
Data were analyzed using one-way ANOVA test and the results with pairwise P values less than 0.05 were considered statistically significant.
A549 cell-derived exosome miR-371b-5p promotes ATIIC-specific proliferation
To further identify the A549-derived key Exo-miR regulating ATIIC-specific proliferation, microarray analysis was performed to characterize A549-specific Exo-miR signature. Purified hiPSC-ATIICs, which exhibit hATIIC-specific miRNA expression pattern (Additional file 1: Figure S1), were used as control. The identified miRNA expression levels were validated by QRT-PCR for consistency. We found 31 Exo-miR molecules secreted by A549 cells. Among these, nine Exo-miRs were differentially expressed between A549 cells and hiPSC-ATIICs (Fig. 2b, indicated with * or #), eight of which (marked with *) expressed at significantly higher levels in A549 cells than in hiPSC-ATIICs. To screen these A549-derived Exo-miRs in an unbiased manner, we generated eight miRNA-inhibitor vectors (Fig. 2c) by using the pSuppressorNeo vector backbone , each designed to express a targeting motif for specific binding to one of the eight highly expressed A549 Exo-miR molecules. We delivered A549-derived Exo-miRs together with one miRNA-inhibitor vector into hESC-derived cells on days 6 and 12, and found that in all cases, A549-derived Exo-miRs lost their capacity to promote ATIIC-specific proliferation when the vector expressing miR-371b-5p inhibitor was co-transfected, as evidenced by a significantly reduced content of SPC-expressing cells, along with a greatly decreased SPC expression level in the cultures (Fig. 2d). Although it could be a concern that the isolated Exo-miR samples may be contaminated with a small amount of mRNAs, our result clearly rules out the role of exosome mRNAs, and suggests a pivotal role of exosome miR-371b-5p-mediated communication between ATIICs in supporting ATIIC-specific proliferation.
Activation of PI3K/Akt signaling pathway in miR-371b-5p mimic-treated hiPSC-ATIICs
To understand the molecular basis of miR-371b-5p-mediated ATIIC-specific proliferation, we examined if PI3K/Akt and/or MAPK/Erk, the two major proliferation-linked signaling pathways , are activated in miR-371b-5p mimic-treated hiPSC-ATIICs. We first tested Akt phosphorylation as an index of PI3K/Akt pathway activation. HiPSC-ATIICs were transfected with various doses of miR-371b-5p mimic, and after 24 hours, phosphorylation was examined using anti-phosphorylated Akt kinase antibody. The miR-371b-5p mimic-treated hiPSC-ATIICs expressed significantly increased levels of phosphorylated Akt kinase protein in a dose-dependent manner (Fig. 3c), suggesting the presence of PI3K-dependent Akt kinase activation [30, 31]. To assess the MAPK/Erk signaling pathway, we analyzed the phosphorylation status of Erk1/2 in the miR-371b-5p mimic-transfected hiPSC-ATIICs and found that these cells did not show a significantly increased expression level of phosphorylated Erk1/2 (Fig. 3d). Next we examined phosphorylation of Akt kinase substrates, and found that treatment with 150 pmol miR-371b-5p mimic stimulated Akt kinase activation, which in turn phosphorylated endogenous GSK3β, FOXO3A, and FOXO1A, as evidenced by significantly increased phosphorylation levels of these proteins (Fig. 3e). These data demonstrate that the PI3K/Akt signaling pathway, but not MAPK/Erk signaling pathway, is activated in miR-371b-5p mimic-treated hiPSC-ATIICs. To further confirm this finding, LY294002 (25 μM), a PI3K inhibitor, was added into the cultures of miR-371b-5p mimic-treated hiPSC-ATIICs for 24 hours. This treatment inhibited phosphorylation of Akt kinase and its substrates (data not shown) and completely blocked the miR-371b-5p mimic-induced cell proliferation (Fig. 3f). Taken together, our data demonstrate that treatment with miR-371b-5p mimic results in activation of PI3K/Akt signaling pathway in hiPSC-ATIICs. As the FOXO factors serve as mediators of apoptosis and cell-cycle arrest , activated Akt kinase that phosphorylates and inhibits transcriptional activity of FOXO factors may account for miR-371b-5p-induced cell proliferation.
MiR-371b-5p mimic promotes ATIIC proliferation by targeting PTEN
ATIICs express exosome miR-371b-5p in vitro and in vivo in response to injury
Relative content of human and mouse ATIICs in bleomycin-mouse lung tissue
1083 ± 54.1
13.2 ± 3.2
14.8 ± 5.2
991 ± 39.8
227.6 ± 11.8
763.4 ± 32.8
Expression of exosome miR-371b-5p in lung lavage of patients with acute pneumonia
Signal pathways derived from niche supporting cells are critical in the regulation of tissue stem/progenitor cell function during development and regeneration. In the lung, several stem/progenitor cell types reside in anatomically diverse regions [47, 48, 49, 50, 51] and likely respond to distinct niche signals for maintenance or repair of functionally and structurally different airway and alveolar epithelia. Identifying niche signaling pathways that regulate lung stem/progenitor cell behavior is key to developing new therapies for targeted activation of endogenous regenerative capacity. However, although extensive effort has been devoted to identifying lung stromal cell-derived niche factors that direct airway stem/progenitor cell fate [52, 53, 54, 55, 56, 57], alveolar niche signal pathways as well as their molecular bases controlling alveolar progenitor ATIIC behavior remain elusive.
We hypothesize that alveolar progenitor ATIICs may derive a functional niche signaling to robustly promote re-epithelialization of injured alveoli. In this present study, we used a differentiating model of pluripotent stem cells to screen ATIIC phenotype-derived signaling and showed that ATIIC line A549-derived exosomes, but not those derived from human normal ATIIC types (hiPSC-ATIICs and hATIICs), mediated a cell-to-cell communication using miRNAs to promote ATIIC-specific proliferation in the pluripotent stem cell-derived cultures. MiRNA expression profiling analysis shows that A549 cells express a phenotype-specific Exo-miR signature. To identify the Exo-miR signaling, we tested each individual A549-specific Exo-miR in an unbiased manner and demonstrated for the first time that exosome miR-371b-5p is the key factor to promote ATIIC-specific proliferation in the pluripotent stem cell-derived cultures by using PTEN as its direct downstream target to activate the PI3K/Akt signaling pathway. Although A549 cell-derived exosomes express a high level of miR-21, which can also target PTEN [58, 59, 60], use of miR-21 inhibitor vector did not affect the capacity of A549 cell-derived Exo-miRs to promote ATIIC-specific proliferation (data not shown), suggesting that exosome miR-21 is not involved in this process. This is because miR-21 is highly expressed by normal ATIIC phenotypes, hiPSC-ATIICs (Fig. 2b) and hATIICs (data not shown), at similar levels. Expression of miR-21 may be required for ATIICs to maintain their basic proliferation capacity as a progenitor cell type. In fact, miR-371b-5p+Exo-miRs promote the cell proliferation in the cultures of ATIIC phenotypes, but not in those of non-ATIIC phenotypes, suggesting more Exo-miRs involved in the complex process of induced ATIIC-specific proliferation in the pluripotent stem cell-derived cultures. How miR-371b-5p works together with other Exo-miRs in a coordinating manner to promote ATIIC-specific proliferation is unknown and merits further investigation, which may provide significant insight into the mechanisms underlying alveolar development/regeneration.
We observed that the BLM-treated hiPSC-ATIICs and hATIICs expressed exosome miR-371b-5p, suggesting a possibility that ATIIC-derived exosome miR-371b-5p may serve as an alveolar niche signaling in response to lung injury. To further test this, we transplanted hiPSC-ATIICs into acute injured mouse lungs, in which the repair capacity of endogenous ATIICs had been eliminated by BLM. As previously reported by our laboratory [1, 2], we showed that the transplanted hiPSC-ATIICs can efficiently engraft and differentiate into ATICs for repair of injured alveoli. Interestingly, the BLM-treated lungs transplanted with hiPSC-ATIICs, but not the BLM-treated lungs and BLM-treated lungs transplanted with hmonos, expressed a significant level of human ATIIC-specific exosome miR-371b-5p, demonstrating the ability of the engrafted hiPSC-ATIICs to derive an Exo-miR signaling in response to lung injury in vivo. Consistent with this finding, a significant level of exosome miR-371b-5p was also detected in injured human lungs. As ATIICs are active in secreting and recycling of vesicle-rich surfactant [17, 61, 62, 63], exosome-mediated communication between ATIICs is thought to be an efficient and robust means to exchange miRNAs for maintaining alveolar homeostasis; in other words, the hiPSC-ATIIC-derived exosome miR-371b-5p in the injured lungs could be efficiently and specifically transferred to neighboring and distant mouse ATIICs to promote the endogenous repair capacity. While we do not have the direct evidence to show Exo-miR-mediated communication between ATIICs in vivo yet, we observed numerous mouse ATIICs survived in BLM-injured lungs that expressed human ATIIC-specific exosome miR-371b-5p, but only a few in the BLM-exposed lungs that were exosome miR-371b-5p negative. Interestingly, our data suggest that those survived mATIICs may also produce miR-292b-5p, the mouse homolog of miR-371b-5p, to participate in the process of re-epithelialization. Collectively, our data strongly suggest that ATIIC-derived exosome miR-371b-5p may contribute to the alveolar signal microenvironment in response to injury, playing a critical role during the re-epithelialization of injured alveoli, and thus may provide a novel target to develop treatment for currently incurable lung diseases.
In summary, we have identified the ATIIC phenotype-derived exosome miR-371b-5p as a key factor that promotes ATIIC-specific proliferation by using PTEN as its direct downstream target to orchestrate the PI3K/Akt signaling pathway. The ATIIC phenotype-derived exosome miR-371b-5p may serve as a niche signaling to promote re-epithelialization of injured lung alveoli in response to injury, and thus provide a novel target to develop treatment for repair of injured alveoli.
We are grateful to Dr. Rick A. Wetsel for his administrative support, and thank Steven Kolodziej and Patricia Navarro for their assistance with the electron microscopy experiments.
This work was supported by University Texas Medical School Bridging Grant Program (DW), the Welch Foundation Endowment in Chemistry and Related Sciences - Grant L-AU-0002 (DW), and the American Heart Association Grant-in-Aid 16GRNT30310015 (DW).
Availability of data and materials
The authors confirm that all data underlying the findings are fully available.
YQ and DW conceived and designed the project, interpreted data, and wrote the manuscript. YQ, ZW, LG, and XP performed differentiation, proliferation, and all molecular biology experiments. DW and JZ performed transplantation experiments. MR, MF, and JLA performed all other experiments and analyzed data. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Animal Welfare Committee of University of Texas Health Science Center at Houston (AWC-15-0180). The hiPSC cell line was generated and published by our group (Yan et al., Stem Cells, 2014), and the de-identified peripheral blood samples were purchased from Gulf Coast Regional Blood Center for NK and monocyte isolation. Generation of the hiPSC cell line, as well as use of the de-identified human lavage samples and the de-identified peripheral blood samples in this project were approved by the University Committee for the protection of Human Subjects (HSC-MS-11-0070). No human subjects were involved and the lavage samples as well as the peripheral blood samples were de-identified, therefore no consent was needed for the project.
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