Rudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany.
Carl-Ludwig-Institute for Physiology, Medical Faculty, Leipzig University, Leipzig, Germany.
Commun Biol. 2024 Jan 16;7(1):104. doi: 10.1038/s42003-024-05783-9.
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.
葡萄糖稳态由胰腺胰岛不同细胞类型分泌的激素维持,并受多种输入信号的控制,包括通过 G 蛋白偶联受体 (GPCR) 介导的信号。RNA-seq 分析显示,在小鼠和人类胰岛中表达了许多 GPCR,其中包括 Gpr116/Adgrf5。GPR116 是一种主要在肺中发现的粘附 GPCR,是表面活性剂分泌所必需的。在这里,我们使用全身和细胞特异性敲除小鼠模型证明 GPR116 参与了胰岛 delta 细胞中生长抑素的释放。有趣的是,全身 GPR116 缺乏会导致进一步的变化,如β细胞质量减少、小胰岛数量减少和胰腺胰岛素含量降低。全身 GPR116 缺乏小鼠的葡萄糖稳态通过调节胰岛素降解的拮抗机制得以维持。我们的数据强调了 GPR116 在控制葡萄糖稳态中的重要功能。