@article{04a35d1c9d6844228f28f7511d4d40c1,
title = "Beta cell primary cilia mediate somatostatin responsiveness via SSTR3",
abstract = "Somatostatin is a paracrine modulator of insulin secretion and beta cell function with pleotropic effects on glucose homeostasis. The mechanism of somatostatin-mediated communication between delta and beta cells is not well-understood, which we address in this study via the ciliary somatostatin receptor 3 (SSTR3). Primary cilia are membrane organelles that act as signaling hubs in islets by virtue of their subcellular location and enrichment in signaling proteins such as G-protein coupled receptors (GPCRs). We show that SSTR3, a ciliary GPCR, mediates somatostatin suppression of insulin secretion in mouse islets. Quantitative analysis of calcium flux using a mouse model of genetically encoded beta cell-specific GCaMP6f calcium reporter shows that somatostatin signaling alters beta cell calcium flux after physiologic glucose stimulation, an effect that depends on endogenous SSTR3 expression and the presence of intact primary cilia on beta cells. Comparative in vitro studies using SSTR isoform antagonists demonstrate a role for SSTR3 in mediating somatostatin regulation of insulin secretion in mouse islets. Our findings support a model in which ciliary SSTR3 mediates a distinct pathway of delta-to-beta cell regulatory crosstalk and may serve as a target for paracrine modulation.",
keywords = "beta cell, calcium, islet, primary cilia, somatostatin, SSTR3",
author = "Adamson, {Samantha E.} and Li, {Zipeng A.} and Jing Hughes",
note = "Funding Information: This study was funded by Endocrine Fellows Foundation grant P20-01465 to SEA and NIH grants DK127748 and DK115795 to JWH. SEA was supported by NIH Institutional National Research Service Award (T32) 5T32DK007120 to Washington University School of Medicine Division of Endocrinology, Metabolism & Lipid Research and supported by Grant Number, K12DK133995 (David Maahs, Linda DiMeglio, Multi-Center Program Directors) from the National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Physician-Scientist Career Development Award. We thank Michael DiGruccio and David Piston for help generating βCKO-GCaMP6 mice. Microscopy work was performed at the Washington University Center for Cellular Imaging (WUCCI), supported by Washington University School of Medicine, The Children{\textquoteright}s Discovery Institute of Washington University and St. Louis Children{\textquoteright}s Hospital (CDI-CORE-2015-505 and CDI-CORE-2019-813) and the Foundation for Barnes-Jewish Hospital (3770 and 4642). Graphical abstract created with BioRender.com. Funding Information: We thank Michael DiGruccio and David Piston for help generating βCKO-GCaMP6 mice. Microscopy work was performed at the Washington University Center for Cellular Imaging (WUCCI), supported by Washington University School of Medicine, The Children{\textquoteright}s Discovery Institute of Washington University and St. Louis Children{\textquoteright}s Hospital (CDI-CORE-2015-505 and CDI-CORE-2019-813) and the Foundation for Barnes-Jewish Hospital (3770 and 4642). Graphical abstract created with BioRender.com. Publisher Copyright: {\textcopyright} 2023 The Author(s). Published with license by Taylor & Francis Group, LLC.",
year = "2023",
doi = "10.1080/19382014.2023.2252855",
language = "English",
volume = "15",
journal = "Islets",
issn = "1938-2014",
number = "1",
}