Glucagon-like peptide 1 elevates cytosolic calcium in pancreatic beta-cells independently of protein kinase A

Glucagon-Like peptide 1 (7-36)amide (GLP-1) is an insulinotropic intestinal peptide hormone with a potential role as antidiabetogenic therapeutic agen t. It mediates a potentiation of glucose-induced insulin secretion, by acti vation of adenylate cyclase and subsequent elevation of cytosolic free calc ium, [Ca2+](cyt). We investigated the role of protein kinase A (PKA) in GLP -1 signal transduction, using isolated mouse islets as well as the differen tiated beta-cell line INS-1. Two specific inhibitors of PKA, (Rp)-adenosine cyclic 3',5'-phosporothioate (Rp-cAMPS, up to 3 mM) and KT5720 (up to 10 m u M), did not inhibit the GLP-1-induced [Ca2+](cyt) elevation. Another PKA inhibitor, H-89, reduced the [Ca2+](cyt) elevation only when applied at hig h concentrations (10-40 mu M), higher than sufficient for PKA inhibition in many cell types. Furthermore, at these concentrations, H-89 also inhibited presumably PKA-independent processes such as glucose-induced [Ca2+](cyt) e levations and intracellular calcium storage. This suggests a PKA-independen t action of H-89. Similarly to H-89, the potent but unselective protein kin ase inhibitor staurosporine inhibited the GLP-1-induced [Ca2+](cyt) elevati on only at high concentrations, at which it also inhibited glucose-induced [Ca2+](cyt) elevations. The same observations as with GLP-1 were made when adenylate cyclase was stimulated with forskolin, for selective examination of signal transduction downstream of receptor and G protein. Our results su ggest that the GLP-1-induced [Ca2+](cyt) elevation is mediated independentl y of PKA and thus belongs to the yet-little-characterized ensemble of effec ts that are mediated by binding of cAMP to other target proteins.