| Literature DB >> 28877479 |
Samuel B Stephens1, Robert J Edwards2, Masato Sadahiro3, Wei-Jye Lin4, Cheng Jiang3, Stephen R Salton5, Christopher B Newgard6.
Abstract
The prohormone VGF is expressed in neuroendocrine and endocrine tissues and regulates nutrient and energy status both centrally and peripherally. We and others have shown that VGF-derived peptides have direct action on the islet β cell as secretagogues and cytoprotective agents; however, the endogenous function of VGF in the β cell has not been described. Here, we demonstrate that VGF regulates secretory granule formation. VGF loss-of-function studies in both isolated islets and conditional knockout mice reveal a profound decrease in stimulus-coupled insulin secretion. Moreover, VGF is necessary to facilitate efficient exit of granule cargo from the trans-Golgi network and proinsulin processing. It also functions to replenish insulin granule stores following nutrient stimulation. Our data support a model in which VGF operates at a critical node of granule biogenesis in the islet β cell to coordinate insulin biosynthesis with β cell secretory capacity.Entities:
Keywords: VGF; chromogranin B; granule biogenesis; insulin secretion; secretory granule; β cell function
Mesh:
Substances:
Year: 2017 PMID: 28877479 PMCID: PMC5624795 DOI: 10.1016/j.celrep.2017.08.050
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423