ENaC acts as a mechanosensor in renal vascular smooth muscle cells that contributes to renal myogenic blood flow regulation, protection from renal injury and hypertension.

Abstract

Pressure-induced constriction (also known as the “myogenic response”) is an important mechanodependent response in small renal arteries and arterioles.  The response is initiated by vascular smooth muscle cell (VSMC) stretch due to an increase in intraluminal pressure and leads to vasoconstriction.  The myogenic response has two important roles as a mechanism of local blood flow autoregulation and protection against systemic blood pressure-induced microvascular damage.  However, the molecular mechanisms underlying initiation of myogenic response are unresolved.  Although several molecules have been considered initiators of the response, our laboratory has focused on the role of degenerin proteins because of their strong evolutionary link to mechanosensing in the nematode.  Our laboratory has addressed the hypothesis that certain degenerin proteins act as mechanosensors in VSMCs.  This article discusses the importance of a specific degenerin protein, b Epithelial Na⁺ Channel (bENaC), in pressure-induced vasoconstriction, renal blood flow and susceptibility to renal injury.  We propose that loss of the renal myogenic constrictor response delays the correction of renal blood flow that occurs with fluctuations in systemic pressure, which allows pressure swings to be transmitted to the microvasculature, thus increasing the susceptibility to renal injury and hypertension. The role of bENaCin myogenic regulation is independentoftubularbENaC and thus represents a non-tubular role for bENaC in renal-cardiovascular homeostasis