Glucose controls glucagon secretion by directly modulating cAMP in alpha cells

• DOI: 10.1007/s00125-019-4857-6
• Publication Date: 2019-04-05T16:28:38Z
• Authors: Qian Yu; Hongyan Shuai; Parvin Ahooghalan...; Erik Gylfe; Anders Tengholm
• Keywords: Male; Enzyme-Linked Immunosorbent Assay; Endocrinology and Diabetes; Article; Mice; 03 medical and health sciences; Protein kinase A; Glucagon release; Cyclic AMP; Animals; Insulin; 0303 health sciences; Pancreatic alpha cell; Glucagon; Cyclic AMP-Dependent Protein Kinases; Hypoglycemia; Mice, Inbred C57BL; Ca2+; Glucose; Glucagon-Secreting Cells; Endokrinologi och diabetes; Calcium; Female; Hypoglycaemia; Somatostatin

Glucagon is critical for normal glucose homeostasis and aberrant secretion of the hormone aggravates dysregulated glucose control in diabetes. However, the mechanisms by which glucose controls glucagon secretion from pancreatic alpha cells remain elusive. The aim of this study was to investigate the role of the intracellular messenger cAMP in alpha-cell-intrinsic glucose regulation of glucagon release.Subplasmalemmal cAMP and Ca2+ concentrations were recorded in isolated and islet-located alpha cells using fluorescent reporters and total internal reflection microscopy. Glucagon secretion from mouse islets was measured using ELISA.Glucose induced Ca2+-independent alterations of the subplasmalemmal cAMP concentration in alpha cells that correlated with changes in glucagon release. Glucose-lowering-induced stimulation of glucagon secretion thus corresponded to an elevation in cAMP that was independent of paracrine signalling from insulin or somatostatin. Imposed cAMP elevations stimulated glucagon secretion and abolished inhibition by glucose elevation, while protein kinase A inhibition mimicked glucose suppression of glucagon release.Glucose concentrations in the hypoglycaemic range control glucagon secretion by directly modulating the cAMP concentration in alpha cells independently of paracrine influences. These findings define a novel mechanism for glucose regulation of glucagon release that underlies recovery from hypoglycaemia and may be disturbed in diabetes.