TRPV4 (Transient Receptor Potential Vanilloid 4) Channel-Dependent Negative Feedback Mechanism Regulates G(q) Protein-Coupled Receptor-Induced Vasoconstriction

TRPV4(瞬时受体电位香草酸受体4)通道依赖性负反馈机制调节G(q)蛋白偶联受体诱导的血管收缩

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Abstract

OBJECTIVE: Several physiological stimuli activate smooth muscle cell (SMC) G(q)PCRs (G(q) protein-coupled receptors) to cause vasoconstriction. As a protective mechanism against excessive vasoconstriction, SMC G(q)PCR stimulation invokes endothelial cell vasodilatory signaling. Whether Ca(2+) influx in endothelial cells contributes to the regulation of G(q)PCR-induced vasoconstriction remains unknown. Ca(2+) influx through TRPV4 (transient receptor potential vanilloid 4) channels is a key regulator of endothelium-dependent vasodilation. We hypothesized that SMC G(q)PCR stimulation engages endothelial TRPV4 channels to limit vasoconstriction. APPROACH AND RESULTS: Using high-speed confocal microscopy to record unitary Ca(2+) influx events through TRPV4 channels (TRPV4 sparklets), we report that activation of SMC α(1)ARs (alpha(1)-adrenergic receptors) with phenylephrine or thromboxane A(2) receptors with U46619 stimulated TRPV4 sparklets in the native endothelium from mesenteric arteries. Activation of endothelial TRPV4 channels did not require an increase in Ca(2+) as indicated by the lack of effect of L-type Ca(2+) channel activator or chelator of intracellular Ca(2+) EGTA-AM. However, gap junction communication between SMCs and endothelial cells was required for phenylephrine activation or U46619 activation of endothelial TRPV4 channels. Lowering inositol 1,4,5-trisphosphate levels with phospholipase C inhibitor or lithium chloride suppressed phenylephrine activation of endothelial TRPV4 sparklets. Moreover, uncaging inositol 1,4,5-trisphosphate profoundly increased TRPV4 sparklet activity. In pressurized arteries, phenylephrine-induced vasoconstriction was followed by a slow, TRPV4-dependent vasodilation, reflecting activation of negative regulatory mechanism. Consistent with these data, phenylephrine induced a significantly higher increase in blood pressure in TRPV4(-/-) mice. CONCLUSIONS: These results demonstrate that SMC G(q)PCR stimulation triggers inositol 1,4,5-trisphosphate-dependent activation of endothelial TRPV4 channels to limit vasoconstriction.

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