| First Author | Vangoitsenhoven R | Year | 2016 |
| Journal | J Steroid Biochem Mol Biol | Volume | 164 |
| Pages | 309-317 | PubMed ID | 26877201 |
| Mgi Jnum | J:323213 | Mgi Id | MGI:6873338 |
| Doi | 10.1016/j.jsbmb.2016.02.011 | Citation | Vangoitsenhoven R, et al. (2016) Effect of a transcriptional inactive or absent vitamin D receptor on beta-cell function and glucose homeostasis in mice. J Steroid Biochem Mol Biol 164:309-317 |
| abstractText | Vitamin D deficiency is associated with beta-cell dysfunction and a higher risk of diabetes, but mice and humans with an absence of the vitamin D receptor (VDR) display normal glucose tolerance. Here, we investigated the direct effects of absence of VDR or absence of ligand activation of VDR on beta-cell function. For this purpose, we generated mice, with a mutation in the AF2 domain of Vdr (VDRDeltaAF2), preventing ligand-driven transcriptional activation of vitamin D responsive genes. VDRDeltaAF2 mice were compared to Vdr full knockout (VDR(-/-)) and wild type (WT) mice. In order to avoid hypocalcemia, which has a direct effect on beta-cell function, mice were fed a high calcium, high lactose diet yielding comparable serum calcium in all mice. While VDR(-/-) mice developed extensive alopecia by the age of 24 weeks, the fur of VDRDeltaAF2 remained normal. All VDRDeltaAF2 mice weighed significantly less than WT, while male but not female VDR(-/-) mice had a lower body weight than WT mice. Dual-energy X-ray absorptiometry showed that both VDRDeltaAF2 (17.2% (females) and 16.6% (males)) and VDR(-/-) (15.7% and 14.8%) mice have a lower percentage of body fat (vs 19.3% and 22.2% in WT). Serum 25(OH)D3 concentrations were lower for both VDRDeltaAF2 (-4.55 fold, P<0.001) and VDR(-/-) (-3.7 fold, P<0.001) as compared to 12 week old WT mice, while serum 1,25(OH)2D3 was increased for both strains 94.5 fold (P<0.01) and 92.8 fold (P<0.001) for VDRDeltaAF2 and VDR(-/-) vs WT, respectively). In vivo glucose tolerance tests performed at 12 and 24 weeks of age, as well as ex vivo glucose stimulated insulin secretion on freshly isolated islets, revealed no major differences between the three strains. Microarray analysis on freshly isolated islets showed only 1 differentially expressed gene, phosphodiesterase 10a (Pde10a), which was 2.16 and 1.75 fold up-regulated in VDRDeltaAF2 and VDR(-/-) islets as compared to WT islets, respectively (P</=0.001). We conclude that in the presence of normocalcemia, absence of VDR or its ligand-activated transcription of genes has no direct regulatory effect on murine glucose homeostasis or gene expression in islets of Langerhans. |
