| First Author | Ohara-Imaizumi M | Year | 2019 |
| Journal | Cell Rep | Volume | 26 |
| Issue | 5 | Pages | 1213-1226.e7 |
| PubMed ID | 30699350 | Mgi Jnum | J:279644 |
| Mgi Id | MGI:6363845 | Doi | 10.1016/j.celrep.2018.12.106 |
| Citation | Ohara-Imaizumi M, et al. (2019) ELKS/Voltage-Dependent Ca(2+) Channel-beta Subunit Module Regulates Polarized Ca(2+) Influx in Pancreatic beta Cells. Cell Rep 26(5):1213-1226.e7 |
| abstractText | Pancreatic beta cells secrete insulin by Ca(2+)-triggered exocytosis. However, there is no apparent secretory site similar to the neuronal active zones, and the cellular and molecular localization mechanism underlying polarized exocytosis remains elusive. Here, we report that ELKS, a vertebrate active zone protein, is used in beta cells to regulate Ca(2+) influx for insulin secretion. beta cell-specific ELKS-knockout (KO) mice showed impaired glucose-stimulated first-phase insulin secretion and reduced L-type voltage-dependent Ca(2+) channel (VDCC) current density. In situ Ca(2+) imaging of beta cells within islets expressing a membrane-bound G-CaMP8b Ca(2+) sensor demonstrated initial local Ca(2+) signals at the ELKS-localized vascular side of the beta cell plasma membrane, which were markedly decreased in ELKS-KO beta cells. Mechanistically, ELKS directly interacted with the VDCC-beta subunit via the GK domain. These findings suggest that ELKS and VDCCs form a potent insulin secretion complex at the vascular side of the beta cell plasma membrane for polarized Ca(2+) influx and first-phase insulin secretion from pancreatic islets. |
