Primary cilia control glucose homeostasis via islet paracrine interactions
Year: 2020
Type: article
Abstract: Pancreatic islets regulate glucose homeostasis through coordinated actions of hormone-secreting cells. What underlies the function of the islet as a unit is the close approximation and communication among heterogeneous cell populations, but the structural mediators of islet cellular cross talk remain incompletely characterized. We generated mice specifically lacking β-cell primary cilia, a cellular organelle that has been implicated in regulating insulin secretion, and found that the β-cell cilia are required for glucose sensing, calcium influx, insulin secretion, and cross regulation of α- and δ-cells. Protein expression profiling in islets confirms perturbation in these cellular processes and reveals additional targets of cilia-dependent signaling. At the organism level, the deletion of β-cell cilia disrupts circulating hormone levels, impairs glucose homeostasis and fuel usage, and leads to the development of diabetes. Together, these findings demonstrate that primary cilia not only orchestrate β-cell-intrinsic activity but also mediate cross talk both within the islet and from islets to other metabolic tissues, thus providing a unique role of cilia in nutrient metabolism and insight into the pathophysiology of diabetes.
Institution: Washington University in St. Louis
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Funders: Children's Discovery Institute, Endocrine Fellows Foundation, National Institutes of Health, Center for Cellular Imaging, Washington University, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Center for Advancing Translational Sciences
Awards: Endoplasmic Reticulum in Beta Cells, Diabetes Research & Training Center, G261815350, Pancreatic Islets Dynamics Regulating Glucagon Secretion, Functional Characterization of WFS1 in Pancreatic beta-cell Viability and Function, Multi-dimensional Dynamics of Pancreatic Islet Cells Measured by Image Mapping diSPIM, GLUCAGON REGULATION BY A NOVEL BROWN ADIPOSE FACTOR, G6639498476, G87705910, G9000153645, G9000217772, G9000258747, Integrated Islet Distribution Program (U24) - 2021, RESOURCE BASED CENTER FOR MUSCULOSKELETAL BIOLOGY AND MEDICINE, Washington University Institute of Clinical and Translational Sciences, Diabetes Research Center
OpenAlex ID: W3014557508
