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anoctamin 6对细胞体积的调节:钙离子、磷脂酶A2与渗透压感知

Cellular volume regulation by anoctamin 6: Ca²⁺, phospholipase A2 and osmosensing.

作者信息

Sirianant Lalida, Ousingsawat Jiraporn, Wanitchakool Podchanart, Schreiber Rainer, Kunzelmann Karl

机构信息

Institut für Physiologie, Universität Regensburg, Universitätsstraße 31, 93053, Regensburg, Germany.

出版信息

Pflugers Arch. 2016 Feb;468(2):335-49. doi: 10.1007/s00424-015-1739-8. Epub 2015 Oct 6.

DOI:10.1007/s00424-015-1739-8
PMID:26438191
Abstract

During cell swelling, Cl(-) channels are activated to lower intracellular Cl(-) concentrations and to reduce cell volume, a process termed regulatory volume decrease (RVD). We show that anoctamin 6 (ANO6; TMEM16F) produces volume-regulated anion currents and controls cell volume in four unrelated cell types. Volume regulation is compromised in freshly isolated intestinal epithelial cells from Ano6-/- mice and also in lymphocytes from a patient lacking expression of ANO6. Ca(2+) influx is activated and thus ANO6 is stimulated during cell swelling by local Ca(2+) increase probably in functional nanodomains near the plasma membrane. This leads to stimulation of phospholipase A2 (PLA2) and generation of plasma membrane lysophospholipids, which activates ANO6. Direct application of lysophospholipids also activates an anion current that is inhibited by typical ANO6 blocker. An increase in intracellular Ca(2+) supports activation of ANO6, but is not required when PLA2 is fully activated, while re-addition of arachidonic acid completely blocked ANO6. Moreover, ANO6 is activated by low intracellular Cl(-) concentrations and may therefore operate as a cellular osmosensor. High intracellular Cl(-) concentration inhibits ANO6 and activation by PLA2. Taken together, ANO6 supports volume regulation and volume activation of anion currents by action as a Cl(-) channel or by scrambling membrane phospholipids. Thereby, it may support the function of LRRC8 proteins.

摘要

在细胞肿胀过程中,氯离子通道被激活以降低细胞内氯离子浓度并减少细胞体积,这一过程称为调节性容积减小(RVD)。我们发现,八聚体蛋白6(ANO6;跨膜蛋白16F)可产生容积调节性阴离子电流,并在四种不相关的细胞类型中控制细胞体积。来自Ano6基因敲除小鼠的新鲜分离的肠上皮细胞以及一名缺乏ANO6表达的患者的淋巴细胞中,容积调节功能受损。细胞肿胀期间,局部钙离子可能在质膜附近的功能性纳米域内增加,从而激活钙离子内流并刺激ANO6。这会导致磷脂酶A2(PLA2)的激活以及质膜溶血磷脂的生成,进而激活ANO6。直接应用溶血磷脂也会激活一种被典型ANO6阻滞剂抑制的阴离子电流。细胞内钙离子的增加有助于ANO6的激活,但当PLA2完全激活时则不需要,而重新添加花生四烯酸会完全阻断ANO6。此外,ANO6可被低细胞内氯离子浓度激活,因此可能作为一种细胞渗透压感受器发挥作用。高细胞内氯离子浓度会抑制ANO6以及PLA2介导的激活。综上所述,ANO6通过作为氯离子通道或通过扰乱膜磷脂来支持容积调节和阴离子电流的容积激活。因此,它可能支持LRRC8蛋白的功能。

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Pflugers Arch. 2014 Oct;466(10):1899-910. doi: 10.1007/s00424-013-1428-4. Epub 2014 Jan 14.
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