Department of Cell Biology and Physiology, University of New Mexico School of Medicine, Albuquerque, New Mexico, USA.
Microcirculation. 2022 Jul;29(4-5):e12774. doi: 10.1111/micc.12774. Epub 2022 Jun 21.
Our previous work demonstrated that endothelial cell (EC) membrane cholesterol is reduced following 48 h of chronic hypoxia (CH). CH couples endothelial transient receptor potential subfamily V member 4 (TRPV4) channels to muscarinic receptor signaling through an endothelium-dependent hyperpolarization (EDH) pathway does not present in control animals. TRVPV4 channel activity has been shown to be regulated by membrane cholesterol. Hence, we hypothesize that acute manipulation of endothelial cell membrane cholesterol inversely determines the contribution of TRPV4 channels to endothelium-dependent vasodilation.
Male Sprague-Dawley rats were exposed to ambient atmospheric (atm.) pressure or 48-h of hypoxia (0.5 atm). Vasodilation to acetylcholine (ACh) was determined using pressure myography in gracilis arteries. EC membrane cholesterol was depleted using methyl-β-cyclodextrin (MβCD) and supplemented with MβCD-cholesterol.
Inhibiting TRPV4 did not affect ACh-induced vasodilation in normoxic controls. However, TRPV4 inhibition reduced resting diameter in control arteries suggesting basal activity. TRPV4 contributes to ACh-induced vasodilation in these arteries when EC membrane cholesterol is depleted. Inhibiting TRPV4 attenuated ACh-induced vasodilation in arteries from CH animals that exhibit lower EC membrane cholesterol than normoxic controls. EC cholesterol repletion in arteries from CH animals abolished the contribution of TRPV4 to ACh-induced vasodilation.
Endothelial cell membrane cholesterol impedes the contribution of TRPV4 channels in EDH-mediated dilation. These results provide additional evidence for the importance of plasma membrane cholesterol content in regulating intracellular signaling and vascular function.
我们之前的工作表明,内皮细胞(EC)膜胆固醇在慢性缺氧(CH)48 小时后会减少。CH 通过内皮依赖性超极化(EDH)途径将内皮瞬时受体电位香草酸亚型 4(TRPV4)通道与毒蕈碱受体信号偶联,而在对照动物中不存在该途径。TRPV4 通道活性受膜胆固醇调节。因此,我们假设急性操纵内皮细胞膜胆固醇会反向确定 TRPV4 通道对内皮依赖性血管舒张的贡献。
雄性 Sprague-Dawley 大鼠暴露于环境大气(atm.)压力或 48 小时缺氧(0.5atm)。用压力肌动描记法在 gracilis 动脉中测定乙酰胆碱(ACh)引起的血管舒张。用甲基-β-环糊精(MβCD)耗尽 EC 膜胆固醇并用 MβCD-胆固醇补充。
在正常氧合对照中,抑制 TRPV4 不影响 ACh 引起的血管舒张。然而,TRPV4 抑制降低了对照动脉中的静息直径,表明存在基础活性。当 EC 膜胆固醇耗尽时,TRPV4 有助于这些动脉中 ACh 引起的血管舒张。在 EC 膜胆固醇低于正常氧合对照的 CH 动物的动脉中,抑制 TRPV4 减弱了 ACh 引起的血管舒张。在 CH 动物的动脉中补充 EC 胆固醇,消除了 TRPV4 对 ACh 引起的血管舒张的贡献。
内皮细胞膜胆固醇阻碍 TRPV4 通道在 EDH 介导的扩张中的作用。这些结果提供了更多证据,证明质膜胆固醇含量在调节细胞内信号和血管功能中的重要性。