| First Author | Alarcon C | Year | 2016 |
| Journal | Diabetes | Volume | 65 |
| Issue | 2 | Pages | 438-50 |
| PubMed ID | 26307586 | Mgi Jnum | J:249444 |
| Mgi Id | MGI:5922172 | Doi | 10.2337/db15-0792 |
| Citation | Alarcon C, et al. (2016) Pancreatic beta-Cell Adaptive Plasticity in Obesity Increases Insulin Production but Adversely Affects Secretory Function. Diabetes 65(2):438-50 |
| abstractText | Pancreatic beta-cells normally produce adequate insulin to control glucose homeostasis, but in obesity-related diabetes, there is a presumed deficit in insulin production and secretory capacity. In this study, insulin production was assessed directly in obese diabetic mouse models, and proinsulin biosynthesis was found to be contrastingly increased, coupled with a significant expansion of the rough endoplasmic reticulum (without endoplasmic reticulum stress) and Golgi apparatus, increased vesicular trafficking, and a depletion of mature beta-granules. As such, beta-cells have a remarkable capacity to produce substantial quantities of insulin in obesity, which are then made available for immediate secretion to meet increased metabolic demand, but this comes at the price of insulin secretory dysfunction. Notwithstanding, it can be restored. Upon exposing isolated pancreatic islets of obese mice to normal glucose concentrations, beta-cells revert back to their typical morphology with restoration of regulated insulin secretion. These data demonstrate an unrealized dynamic adaptive plasticity of pancreatic beta-cells and underscore the rationale for transient beta-cell rest as a treatment strategy for obesity-linked diabetes. |
