Paired box 6 (PAX6) regulates glucose metabolism via proinsulin processing mediated by prohormone convertase 1/3 (PC1/3)
- First Online:
- Cite this article as:
- Wen, J.H., Chen, Y.Y., Song, S.J. et al. Diabetologia (2009) 52: 504. doi:10.1007/s00125-008-1210-x
- 900 Downloads
Human patients with aniridia caused by heterozygous PAX6 mutations display abnormal glucose metabolism, but the underlying molecular mechanism is largely unknown. Disturbed islet architecture has been proposed as the reason why mice with complete inactivation of paired box 6 (PAX6) in the pancreas develop diabetes. This is not, however, the case in human aniridia patients with heterozygous PAX6 deficiency and no apparent defects in pancreatic development. We investigated the molecular mechanism underlying the development of abnormal glucose metabolism in these patients.
A human aniridia pedigree with a PAX6 R240Stop mutation was examined for abnormal glucose metabolism using an OGTT. The underlying mechanism was further investigated using Pax6 R266Stop mutant small-eye mice, which also have abnormal glucose metabolism similar to that in PAX6 R240Stop mutation human aniridia patients.
Paired box 6 (PAX6) deficiency, both in aniridia patients with a heterozygous PAX6 R240Stop mutation and in mice with a heterozygous Pax6 R266Stop mutation, causes defective proinsulin processing and abnormal glucose metabolism. PAX6 can bind to the promoter and directly upregulate production of prohormone convertase (PC)1/3, an enzyme essential for conversion of proinsulin to insulin. Pax6 mutations lead to PC1/3 deficiency, resulting in defective proinsulin processing and abnormal glucose metabolism.
This study indicates a novel function for PAX6 in the regulation of proinsulin processing and glucose metabolism via modulation of PC1/3 production. It also provides an insight into the abnormal glucose metabolism caused by heterozygous PAX6 mutations in humans and mice.
KeywordsGlucose metabolismPAX6PC1/3Proinsulin processing
Impaired glucose tolerance
Intraperitoneal glucose tolerance test
Alpha-melanocyte stimulating hormone
Paired box 6
Quantitative reverse transcription PCR
Single-strand conformational polymorphism
PAX6 encodes a transcription factor and belongs to the paired-box gene family. The protein contains a paired domain, a linker region, a homeodomain and a transactivation region [1, 2]. The paired domain together with the homeodomain binds to the promoter DNA, allowing the transactivation region to regulate the expression of its target gene [3, 4].
Paired box 6 (PAX6) is an evolutionarily conserved protein whose amino acid sequences are almost identical between humans and mice . The Pax6-null mutant mouse has defects in the development of the eye, brain and pancreas, leading to neonatal lethality [6–10]. Mice with heterozygous Pax6 mutations can survive but show a phenotype of small eyes . This small-eye phenotype mirrors the condition seen in human aniridia patients, who are characterised by lack of irises caused by heterozygous PAX6 gene mutations [9, 10].
In 2002, it was reported that four sporadic aniridia patients with PAX6 mutations developed impaired glucose tolerance (IGT) , but the mechanism of how PAX6 heterozygosity leads to abnormal glucose metabolism is still unclear. Another study showed that mice with a complete loss of PAX6 in the pancreas developed diabetes ; these mutant mice exhibited disturbed islet architecture, suggesting that diabetes in Pax6 mutant mice is due to abnormal pancreatic development [7, 12, 13]. This, however, is not the case in heterozygous Pax6 mutant animals, which do not show apparent defects in pancreatic development . Therefore, it is still largely unknown why aniridia patients with PAX6 mutations develop abnormal glucose metabolism.
To address these questions, we investigated an extended aniridia family and identified a pedigree carrying a heterozygous PAX6 gene mutation. We also obtained mutant mice that had both the Pax6 gene mutation and the small-eye phenotype. Using this heterozygous Pax6 mutant mouse model, we further investigated how the Pax6 gene mutation caused abnormal glucose metabolism in these mice and probably in the human aniridia patients, too.
Participants: identification of a pedigree with the PAX6 gene mutation
The family with aniridia was identified at Peking University Third Hospital. This study was approved by the Ethics Committee of Peking University Health Science Center and carried out according to the guidelines of the World Medical Association Declaration of Helsinki (www.wma.net/e/policy/b3.htm). All participants (or their parents) were fully aware of the scope of this study and signed an informed consent form prior to enrolment.
Collection of human and mouse blood samples
Venous blood samples were collected from all available members in the family at fasting and at 30, 60 and 120 min after glucose loading. The amount of glucose ingested for adults was 75 g per person. For children this was adjusted according to the formula 1.75 g/kg body weight, with total intake held to less than 75 g. Genomic DNA was prepared from venous blood samples.
For the intraperitoneal glucose tolerance test (IPGTT) in mice, the blood samples were collected at fasting and at 30, 60 and 120 min after injection of glucose. Blood samples were collected from the tail vein into tubes containing anticoagulant (about 1,000 U of heparin per millilitre of blood). Immediately after centrifugation (2,500 g) at 4°C, plasma was separated and stored at −70°C for further analysis.
Measurement of plasma total insulin, proinsulin, adrenocorticotropic hormone and α-melanocyte stimulating hormone
Human insulin and proinsulin levels were measured with RIA kits (Linco Research, St Charles, MO, USA). Specific electroimmunoassay (EIA) kits from Phoenix Pharmaceuticals (Mountain View, CA, USA) were used to detect adrenocorticotropic hormone (ACTH) and alpha-melanocyte stimulating hormone (α-MSH) levels in humans. The American Diabetes Association criteria were used for diagnosis of IGT and diabetes [17, 18].
Mouse insulin was measured with an ELISA kit from Shibayagi Company (Ishihara Shibukawa-shi, Gumma, Japan). Mouse proinsulin was measured using an ELISA kit for rat proinsulin (Mercodia, Uppsala, Sweden) according to the manufacturer’s instructions. Since this kit is for rat proinsulin, the calculated ratios of proinsulin over total insulin in mice are likely to be not precise, but are acceptable for the present purposes of comparison. Specific EIA kits and protocols (Phoenix Pharmaceuticals, Mountain View, CA, USA) were used to measure levels of ACTH and α-MSH in tissue extracts of mice.
Animals, N-ethyl-N-nitrosourea mutagenesis, mapping and genotyping
C57BL/6J and C3H/HeJ mice were obtained from the Jackson Laboratory (Bar Harbor, ME, USA). Injection of the chemical mutagen N-ethyl-N-nitrosourea into male mice often induces sporadic A–T transition in the germ cell genome of the animals. After breeding with normal mice, the mutation can be transmitted to newborns. Based on the small-eye phenotype, mice with the Pax6 gene mutation can be selected. The mutant mice were crossed to C3H/HeJ to generate F1 mice. The F1 mice with the small-eye phenotype were back-crossed to C57BL/6J to generate F2. Tail DNA samples of F2 mice were extracted and PCR-amplified with D2Mit249 micro-satellite marker of the Whitehead/MIT database (http://www-genome.wi.mit.edu). PCR products were separated by electrophoresis with 4% (wt/vol.) agarose II gel (BioBasic, Toronto, ON, Canada). Mice were genotyped by PCR analysis with primers specific for Pax6: forward primer 5′-GATGAGATGGGAGTTGGGTG-3′, reverse primer: 5′-AAGTTACCAGGTGTGGTGGG-3′.
Mice were maintained in a pathogen-free facility under a 12 h light–dark cycle and were given free access to food and water. The studies were approved by the Peking University animal ethics committee. Animal experiments were carried out in accordance with institutional guidelines and complied with The 1996 Guide for the Care and Use of Laboratory Animals .
IPGTT and insulin tolerance test in mice
After fasting for about 15 h, baseline blood glucose levels were measured. The glucose solution (20%, wt/vol.) was then injected intraperitoneally at 10 μl/g body weight and blood glucose levels were measured at 30, 60 and 120 min after the injection. For the insulin tolerance test, mice were fasted for 6 h and then injected with human insulin (Novo-Nordisk, Bagsværd, Denmark) at 0.75 U/kg body weight. Blood glucose levels were measured at fasting and at 15, 30, 45 and 60 min following insulin injections. Blood glucose concentrations were measured with a One Touch Ultra meter (Lifescan, Milpitas, CA, USA).
Isolation and purification of mouse islets
The islets of mice were isolated and characterised following the method of Hori . Briefly, the pancreas was digested by type V collagenase (Sigma-Aldrich, St Louis, MO, USA) and then purified by centrifugation (2,700 g) on Histopaque-1077 gradients (Sigma-Aldrich). Individual islets, free of attached acinar, vascular and ductal tissues, were handpicked under a dissecting microscope.
The mouse pancreas was fixed for 10 h in 4% (wt/vol.) paraformaldehyde/PBS at 4°C before cryosection. The cryosections were immunostained with normal rabbit or mouse IgG, rabbit antibody to glucagon or mouse antibody to insulin (Zhongshan Goldenbridge Biotechnology, Beijing, China) and incubated overnight at 4°C with anti-rabbit IgG or anti-mouse IgG, and then with mounting medium (DAPI; Vector Laboratories, Burlingame, CA, USA).
NIT-1 mouse insulinoma cells were cultured in RPMI 1640 with 10% (vol./vol.) FBS. NIH3T3 cells were cultured in DMEM/High Glucose with 10% (vol./vol.) FBS. All cell culture media were obtained from Gibco BRL (Gaithersburg, MD, USA) and the FBS from Hyclone (Thermo Fisher Scientific, Waltham, MA, USA).
RNA of islets was extracted with RNeasy Micro Kit (Qiagen, Valencia, CA, USA) and reversed to cDNA. The quantitative RT-PCR (qRT-PCR) was performed with primers specific for Pc1/3 (also known as Pcsk1): forward primer 5′-ATGGGCGGCGGAGATC-3′, reverse primer 5′-CCAATCTGACCCAAAAGGTCATAC-3′. GAPDH was used as a control: forward primer 5′-GCACCACCAACTGCTTAGC-3′, reverse primer 5′-TCTTCTGGGTGGCAGTGATG-3′.
Western blotting analysis
The proteins of islets were separated by 10% (wt/vol.) SDS-PAGE and probed with different antibodies including rabbit PAX6-specific antibody (Chemicon, Temecula, CA, USA), rabbit prohormone convertase (PC)1/3-specific antibody (Abcam, Cambridge, MA, USA) and mouse β-actin-specific monoclonal antibody (Sigma-Aldrich).
Luciferase reporter assay
A 4,194-bp mouse Pc1/3 promoter sequence was cloned from mouse genomic DNA and inserted into pGL3-basic luciferase reporter vectors. The primers were as follows: forward primer 5′-CGGGGTACCGGGCTGGGAAGGAATAAAATCTGGAGTATAAA-3′, reverse primer 5′-CCGCTCGAGTCTTGACGTCAGATCTACCTGGACTGAGAACTGGAT-3′. Pax6 was cloned and inserted into pcDNA3.1 (−) vectors. The luciferase reporter assay was performed in NIH3T3 cells. The cells were cultivated in 24 well plates for 24 h and transfected by transfection reagent (Lipofectamine 2000; Invitrogen, Carlsbad, CA, USA) with the mouse Pc1/3 promoter along with either intact or mutated Pax6 cDNA at several doses. Cells were collected 48 h after transfection and assayed in triplicate with the Dual-Luciferase Reporter Assay System (Promega, Madison, WI, USA).
Chromatin immunoprecipitation assays
Chromatin immunoprecipitation (ChIP) assays were performed in a mouse beta cell line, NIT-1 cells from the American Type Culture Collection (ATCC, Manassas, VA, USA). Briefly, the chemical-linked complexes of genomic DNA and PAX6 protein were immunoprecipitated with antibodies specific to PAX6 (Chemicon). The DNA was amplified after ChIP using primers of Pc1/3 promoter (forward primer 5′-TCATCAAGTCTTGCCTCGTT-3′, reverse primer 5′-ATTATCGCTGTCCACACAT-3′).
Statistical analysis was performed using an independent samples t test. Differences were considered statistically significance at p < 0.05.
A heterozygous PAX6 R240Stop mutation was identified in the aniridia pedigree; affected patients exhibited abnormal proinsulin processing and impaired glucose tolerance
To determine whether there was any mutation in the PAX6 gene in the identified pedigree, we first narrowed down the region bearing a potential mutation to exon 9 of the PAX6 gene by SSCP (not shown). Within exon 9 we identified a C-to-T mutation at nucleotide 1080 that converted an Arg codon (CGA) to a stop codon (TGA; Fig. 1b). This mutation resulted in a truncated polypeptide that prematurely terminated at residue 240 (PAX6 R240Stop mutation; hereafter referred to as the PAX6 mutation; Fig. 1c), whereas the full length PAX6 consists of 422 amino acids (Fig. 1c). The R240Stop truncated polypeptide lacked the entire transactivation domain and a small portion of the homeodomain (Fig. 1c). The mutation was not found in the four unaffected consanguineous family members or in the sample of 100 unaffected people.
Total insulin levels (including proinsulin and true insulin) in the blood of patients with the PAX6 mutation were significantly lower than those in the controls post glucose loading (Fig. 2e). At 2 h after the glucose challenge, total insulin production in the patients with the PAX6 mutation finally caught up with the levels in the controls (Fig. 2e); nonetheless, blood glucose levels in the same patients with the PAX6 mutation remained high (Fig. 2c). This suggests that these patients might have defects in insulin production and insulin signalling. To exclude the latter possibility, an insulin tolerance test was performed. The participants received an insulin injection and blood glucose levels were measured at different time points. As shown in Fig. 2f, patients with the PAX6 mutation and controls showed no difference in terms of insulin sensitivity. Interestingly, the blood proinsulin levels (Fig. 2g) and the proinsulin/C-peptide ratios (ESM Fig. 1) were much higher in both diabetic patients and in the patients with the PAX6 mutation than in the controls.
Although blood proinsulin levels in the patients with the PAX6 mutation were lower than in the patients with type 2 diabetes (Fig. 2g), the proinsulin/total insulin ratio in the former was significantly higher than in the latter (Fig. 2h). Similar results were also observed when the patients with the PAX6 mutation were subdivided into groups with (1) normal glucose metabolism and (2) abnormal glucose metabolism, i.e. either IGT or diabetes (ESM Fig. 2). Therefore, unlike in the type 2 diabetes patients whose high proinsulin levels may be due to overstimulation by hyperglycaemia [21, 22], the high proinsulin levels in the patients with the PAX6 mutation most probably resulted from a defect in proinsulin processing. In other words, defective proinsulin processing may be the primary cause for development of abnormal glucose metabolism in patients with the PAX6 mutation.
Cleavage of proinsulin mainly depends on prohormone convertases. Both PC1/3 and PC2 are members of a family of serine proteases encoded on human chromosome 5q14-q21and 20p11.2, respectively [23, 24]. While pancreatic alpha cells mainly produce PC2, pancreatic beta cells produce PC1/3 and PC2 [25–27]. Based on the pedigree study, we hypothesised that PAX6 may regulate the production of the PCs and that the PAX6 gene mutation causes PC deficiency, leading to defective proinsulin processing and, in turn, abnormal glucose metabolism.
Pax6 heterozygous R266Stop mutant mice exhibited abnormal glucose metabolism similar to that in the human patients with the PAX6 mutation
These mutant mice did not show obvious structural abnormalities in the pancreas (Fig. 3b) as revealed by immunofluorescent staining of insulin and glucagon. Glucose metabolism as measured by IPGTT appeared to be nearly normal in these mutant mice when younger than 4 months (Fig. 3c). However, when older than 6 months, most of these Pax6 mutant mice, like patients with the PAX6 mutation above 35 years of age in the pedigree (Fig. 2d), exhibited IGT detected by IPGTT (Fig. 3c), but responded normally to exogenous insulin (Fig. 3d). Similarly to the patients with the PAX6 mutation, the proinsulin/total insulin ratios in the Pax6 mutant mice were significantly higher than in wild-type controls (Fig. 3e). Actually, a high proinsulin/total insulin ratio was also observed in mutant mice at age 4 months that had not shown abnormalities at 120 min in the IPGTT (Fig. 3c,e). These observations indicate that the abnormal proinsulin/total insulin ratio was present before the development of abnormal glucose metabolism in the Pax6 mutant mice.
In analysing glucose metabolism in these mutants, we documented that the Pax6 mutant mice share a similarity with the human aniridia patients with the PAX6 mutation with regard to abnormal glucose metabolism. Using this animal model, we then investigated whether PCs are deficient and if so, how the Pax6 mutation leads to such a deficiency.
PAX6 directly regulates PC1/3 levels and the Pax6 mutation leads to PC1/3 deficiency
To investigate how the Pax6 mutation leads to PC1/3 deficiency, we performed a luciferase reporter assay using Pc1/3 promoter activity as the variable. PAX6, but not the truncated moiety, was found to promote the expression of Pc1/3 in a dose-dependent manner (Fig. 4c). In agreement with these data, we detected the binding of PAX6 to the Pc1/3 promoter by ChIP assay (Fig. 4d) in NIT-1 cells [29, 30]. We therefore concluded that the Pax6 mutation caused PC1/3 deficiency, leading to defective proinsulin processing. Since the truncated PAX6 polypeptide did not show any effect on Pc1/3 expression (Fig. 4c), we concluded that the Pax6 mutation leading to PC1/3 deficiency is a dose-dependent phenomenon rather than a dominant negative effect.
ACTH and α-MSH were decreased in the blood of the aniridia patients with the PAX6 mutation as well as in the brain of Pax6 mutant mice
Based on our investigation of aniridia patients with the heterozygous PAX6 mutation and of small-eye mice with the Pax6 mutation, we demonstrated that the PAX6 mutation causes a decrease in PC1/3. The resulting PC1/3 deficiency leads to defective proinsulin processing and subsequent abnormal glucose metabolism. This study thus indicates a novel function for PAX6 in the regulation of proinsulin processing and glucose metabolism via modulation of PC1/3 production.
Our finding is consistent with studies by Yasuda et al.  and Ashery-Padan et al.  in that PAX6 deficiency leads to abnormal glucose metabolism in mice and in humans. Moreover, we provide evidence that PAX6 mutations cause PC1/3 deficiency, resulting in defective proinsulin processing and subsequent abnormal glucose metabolism. This conclusion is partially supported by the fact that PC1/3 deficiency causes abnormal glucose metabolism in humans and mice [32–35]. However, the phenotype and the primary mechanism may be different. For instance, human patients with PC1/3 mutation or mice with Pc1/3 N222D/N222D mutation exhibited significant obesity [33, 35]. In our study, we saw no obesity either in the Pax6 mutant mice or in the patients with the PAX6 mutation, as evidenced by their normal BMI (ESM Table 1), even though α-MSH levels were decreased in the human and mice mutant groups. This observation is in relative agreement with what is seen in Pc1-null mice, which showed α-MSH deficiency but did not develop obesity . It appears that an obese phenotype such as this depends on the dosage of PC1/3, since mice with PC1/3 hemizygous deficiency indeed exhibited mild obesity .
It has been reported that Pax6sey/sey mice with homozygous Pax6 mutation exhibited decreased levels of glucagon-like peptide-1 (GLP-1) in the small and large intestine . However, we did not detect significant differences in GLP-1 production in the patients with the mutation versus normal controls (not shown). One possible explanation is that, unlike in mouse intestine, PAX6 may not be present in significant amounts in adult human intestinal cells, as suggested by a published study . Compared with its production in human pancreas, PAX6 expression was barely detected in human intestine . Moreover, we found that all IVGTT measurements were very similar to those from the OGTT (ESM Fig. 3). These data indicate that the abnormal glucose metabolism we observed in this study cannot be due to changes in the intestinal GLP-1 level.
Since PAX6 controls many downstream events, the primary cause of abnormal glucose metabolism in the PAX6-deficient participants may differ from that in the PC1/3-deficient animals. Some of the downstream factors regulated by PAX6 may play a role opposed to that of α-MSH in the regulation of food intake; even though both PC1/3 and α-MSH were reduced in our participants, we did not observe obesity in those with the PAX6 mutation. The definitive explanation of these discrepancies awaits further investigation.
Using PAX6-deficient mouse models, several previous studies have proposed that the disturbed architecture and the resulting deficiency in insulin production in pancreas is the reason why mutant mice develop diabetes [7, 12, 13]. In heterozygous Pax6 mutant mice, however, we did not see any obviously abnormal pancreatic architecture (Fig. 3b) . Instead, we found that the proinsulin/total insulin ratio both in the patients with the PAX6 mutation (Fig. 2g,h) and in the Pax6 mutant mice was significantly higher than in wild-type controls (Fig. 3e). Furthermore, we found that, even though type 2 diabetes patients often have high proinsulin levels due to overstimulation by hyperglycaemia [21, 22], the proinsulin/total insulin ratio in the patients with the heterozygous PAX6 mutation was significantly higher than in the type 2 diabetes patients (Fig. 2h), suggesting, again, that defective proinsulin processing may be the primary cause of diabetes in the patients with the PAX6 mutation. This observation of the effect of the PAX6 mutation is partially supported by a report that a point mutation in the human insulin gene gives rise to abnormal glucose metabolism and hyperproinsulinaemia .
It is important to note that the majority of the Pax6 mutant mice and the patients with the PAX6 mutation did not develop IGT until advanced ages. For example, most patients with the PAX6 mutation exhibited abnormal glucose metabolism at ages above 35 years (Fig. 2d), which was similar to the comparative age (>6 months) at which abnormal glucose metabolism appeared in Pax6 mutant mice (Fig. 3c), suggesting that other age-dependent factors may possibly exist and work in coordination with PAX6 in the regulation of glucose metabolism. This also raises an interesting question regarding proinsulin levels in the participants with the heterozygous mutation in PAX6 who did not yet show abnormal glucose metabolism. Before age 4 months, the Pax6 mutant mice did not show significant differences from wild-type mice in blood glucose levels during the IPGTT (Fig. 3c), but did exhibit higher proinsulin/total insulin ratio than wild-type animals (Fig. 3e). Therefore the high ratio of proinsulin/ total insulin in the Pax6 mutant mice occurs prior to onset of abnormal glucose metabolism, suggesting, again, defective proinsulin processing as the cause rather than an effect of abnormal glucose metabolism in the animals with the heterozygous Pax6 mutation. The presence of such additional factors that contribute to the development of abnormal glucose metabolism in the animals with the Pax6 mutation is currently under further investigation.
Glucose metabolism is an extraordinarily complex process that is regulated by multiple mechanisms. Our conclusion that defective proinsulin processing causes abnormal glucose metabolism in the participants with PAX6 mutations does not exclude the possibility that other mechanisms, such as the α-MSH regulatory pathway, may also contribute to the disorder. Nonetheless, our study provides a novel function of PAX6 in the regulation of proinsulin processing and glucose metabolism via modulation of PC1/3 production. It also provides an insight into how PAX6 mutations lead to abnormal glucose metabolism in mice and humans.
We thank D. Stenger (Barbara Davis Center, University of Colorado, Denver, CO, USA) and L. H. Li (Stowers Institute for Medical Research, Kansas City, MO, USA) for their comments and suggestions. This work was supported by grants from the Chinese National 863 Projects (2006AA02A114), Beijing Ministry of Science and Technology (D07050701350704) and the Chinese National 973 Projects (2006CB943603) to L. S. Li, and the Chinese National 973 Projects (2006CB503905) to Peking University Stem Cell Research Center. It was also supported by grants from the Ministry of Science and Technology for International Collaboration Project 20070192 to the China–Australian Center of Excellence for Stem Cell Sciences, a grant from Natural Science Foundation of Beijing (7062067) to T. P. Hong and grants from the National Natural Science Foundation of China to J. H. Wen (30871251) and to C. Y. Zhang (Outstanding Young Scientist Award 30225037).
Duality of interest
The authors declare that there is no duality of interest associated with this manuscript.