The adhesion GPCR GPR116/ADGRF5 has a dual function in pancreatic islets regulating somatostatin release and islet development

粘附 GPCR GPR116/ADGRF5 在胰腺胰岛中具有调节生长抑素释放和胰岛发育的双重功能

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作者:Juliane Röthe, Robert Kraft, Albert Ricken, Isabell Kaczmarek, Madlen Matz-Soja, Karsten Winter, André Nguyen Dietzsch, Julia Buchold, Marie-Gabrielle Ludwig, Ines Liebscher, Torsten Schöneberg, Doreen Thor

Abstract

Glucose homeostasis is maintained by hormones secreted from different cell types of the pancreatic islets and controlled by manifold input including signals mediated through G protein-coupled receptors (GPCRs). RNA-seq analyses revealed expression of numerous GPCRs in mouse and human pancreatic islets, among them Gpr116/Adgrf5. GPR116 is an adhesion GPCR mainly found in lung and required for surfactant secretion. Here, we demonstrate that GPR116 is involved in the somatostatin release from pancreatic delta cells using a whole-body as well as a cell-specific knock-out mouse model. Interestingly, the whole-body GPR116 deficiency causes further changes such as decreased beta-cell mass, lower number of small islets, and reduced pancreatic insulin content. Glucose homeostasis in global GPR116-deficient mice is maintained by counter-acting mechanisms modulating insulin degradation. Our data highlight an important function of GPR116 in controlling glucose homeostasis.

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