The adhesion GPCR GPR116/ADGRF5 has a dual function in pancreatic islets regulating somatostatin release and islet development.
Juliane RötheRobert KraftAlbert RickenIsabell KaczmarekMadlen Matz-SojaKarsten WinterAndré Nguyen DietzschJulia BucholdMarie-Gabrielle LudwigInes LiebscherTorsten SchönebergDoreen ThorPublished in: Communications biology (2024)
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.
Keyphrases
- single cell
- rna seq
- fatty acid
- type diabetes
- mouse model
- cell therapy
- endothelial cells
- induced apoptosis
- signaling pathway
- blood pressure
- escherichia coli
- mesenchymal stem cells
- glycemic control
- electronic health record
- cell cycle arrest
- binding protein
- long non coding rna
- cell death
- deep learning
- smoking cessation
- artificial intelligence
- neuroendocrine tumors
- data analysis
- pluripotent stem cells