Conventional and Unconventional Mechanisms for Soluble Guanylyl Cyclase Signaling

Abstract

Soluble guanylyl cyclase (sGC) is the principal enzyme in mediating the biological actions of nitric oxide. On activation, sGC converts guanosine triphosphate to guanosine 3′,5′-cyclic monophosphate (cGMP), which mediates diverse physiological processes including vasodilation, platelet aggregation, and myocardial functions predominantly by acting on cGMP-dependent protein kinases. Cyclic GMP has long been considered as the sole second messenger for sGC action. However, emerging evidence suggests that, in addition to cGMP, other nucleoside 3′,5′-cyclic monophosphates (cNMPs) are synthesized by sGC in response to nitric oxide stimulation, and some of these nucleoside 3′,5′-cyclic monophosphates are involved in various physiological activities. For example, inosine 3′,5′-cyclic monophosphate synthesized by sGC may play a critical role in hypoxic augmentation of vasoconstriction. The involvement of cytidine 3′,5′-cyclic monophosphate and uridine 3′,5′-cyclic monophosphate in certain cardiovascular activities is also implicated.