| First Author | Fan F | Year | 2015 |
| Journal | J Clin Invest | Volume | 125 |
| Issue | 11 | Pages | 4026-41 |
| PubMed ID | 26413867 | Mgi Jnum | J:227493 |
| Mgi Id | MGI:5700592 | Doi | 10.1172/JCI80652 |
| Citation | Fan F, et al. (2015) Dynamin 2 regulates biphasic insulin secretion and plasma glucose homeostasis. J Clin Invest 125(11):4026-41 |
| abstractText | Alterations in insulin granule exocytosis and endocytosis are paramount to pancreatic beta cell dysfunction in diabetes mellitus. Here, using temporally controlled gene ablation specifically in beta cells in mice, we identified an essential role of dynamin 2 GTPase in preserving normal biphasic insulin secretion and blood glucose homeostasis. Dynamin 2 deletion in beta cells caused glucose intolerance and substantial reduction of the second phase of glucose-stimulated insulin secretion (GSIS); however, mutant beta cells still maintained abundant insulin granules, with no signs of cell surface expansion. Compared with control beta cells, real-time capacitance measurements demonstrated that exocytosis-endocytosis coupling was less efficient but not abolished; clathrin-mediated endocytosis (CME) was severely impaired at the step of membrane fission, which resulted in accumulation of clathrin-coated endocytic intermediates on the plasma membrane. Moreover, dynamin 2 ablation in beta cells led to striking reorganization and enhancement of actin filaments, and insulin granule recruitment and mobilization were impaired at the later stage of GSIS. Together, our results demonstrate that dynamin 2 regulates insulin secretory capacity and dynamics in vivo through a mechanism depending on CME and F-actin remodeling. Moreover, this study indicates a potential pathophysiological link between endocytosis and diabetes mellitus. |
