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首页> 外文期刊>American Journal of Physiology >RhoA exerts a permissive effect on volume-regulated anion channels in vascular endothelial cells.
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RhoA exerts a permissive effect on volume-regulated anion channels in vascular endothelial cells.

机译:RhoA对血管内皮细胞中体积调节的阴离子通道具有宽容作用。

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摘要

Cell swelling triggers in most cell types an outwardly rectifying anion current, I(Cl,swell), via volume-regulated anion channels (VRACs). We have previously demonstrated in calf pulmonary artery endothelial (CPAE) cells that inhibition of the Rho/Rho kinase/myosin light chain phosphorylation pathway reduces the swelling-dependent activation of I(Cl,swell). However, these experiments did not allow us to discriminate between a direct activator role or a permissive effect. We now show that the Rho pathway did not affect VRAC activity if this pathway was activated by transfecting CPAE cells with constitutively active isoforms of Galpha (a Rho activating heterotrimeric G protein subunit), Rho, or Rho kinase. Furthermore, biochemical and morphological analysis failed to demonstrate activation of the Rho pathway during hypotonic cell swelling. Finally, manipulating the Rho pathway with either guanosine 5'-O-(3-thiotriphosphate) or C3 exoenzyme had no effect on VRACs in caveolin-1-expressing Caco-2 cells. We conclude that the Rho pathway exerts a permissive effect on VRACs in CPAE cells, i.e., swelling-induced opening of VRACs requires a functional Rho pathway, but not an activation of the Rho pathway.
机译:在大多数细胞类型中,细胞膨胀都会通过体积调节的阴离子通道(VRAC)触发向外整流的阴离子电流I(Cl,swell)。我们以前在小腿肺动脉内皮(CPAE)细胞中证实,Rho / Rho激酶/肌球蛋白轻链磷酸化途径的抑制作用可降低I(Cl,swell)的溶胀依赖性激活。但是,这些实验不允许我们区分直接的激活剂作用或允许的作用。我们现在显示,如果通过用Galpha(Rho激活异源三聚体G蛋白亚基),Rho或Rho激酶的组成型活性同工型转染CPAE细胞激活该途径,则Rho途径不会影响VRAC活性。此外,生化和形态学分析未能证明低渗细胞肿胀过程中Rho途径的激活。最后,用鸟苷5'-O-(3-硫代三磷酸)或C3外切酶操纵Rho途径对表达caveolin-1的Caco-2细胞中的VRAC没有影响。我们得出的结论是,Rho途径对CPAE细胞中的VRAC发挥了放任的作用,即溶胀诱导的VRACs的开放需要功能性Rho途径,而不是Rho途径的激活。

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