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LRRC8 Proteins Form Volume-Regulated Anion Channels that Sense Ionic Strength

机译:LRRC8蛋白形成可调节离子强度的体积调节阴离子通道

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The volume-regulated anion channel (VRAC) is activated when a cell swells, and it plays a central role in maintaining cell volume in response to osmotic challenges. SWELL1 (LRRC8A) was recently identified as an essential component of VRAC. However, the identity of the pore-forming subunits of VRAC and how the channel is gated by cell swelling are unknown. Here, we show that SWELL1 and up to four other LRRC8 subunits assemble into heterogeneous complexes of similar to 800 kDa. When reconstituted into bilayers, LRRC8 complexes are sufficient to form anion channels activated by osmolality gradients. In bilayers, as well as in cells, the single-channel conductance of the complexes depends on the LRRC8 composition. Finally, low ionic strength (Gamma) in the absence of an osmotic gradient activates the complexes in bilayers. These data demonstrate that LRRC8 proteins together constitute the VRAC pore and that hypotonic stress can activate VRAC through a decrease in cytoplasmic Gamma.
机译:体积膨胀的阴离子通道(VRAC)在细胞膨胀时被激活,它在维持细胞体积以应对渗透挑战方面起着核心作用。 SWELL1(LRRC8A)最近被确定为VRAC的重要组成部分。但是,尚不清楚VRAC的孔形成亚基的身份以及细胞溶胀如何控制通道。在这里,我们显示SWELL1和多达四个其他LRRC8亚基组装成类似800 kDa的异构复合物。当重构为双层时,LRRC8络合物足以形成由渗透压梯度激活的阴离子通道。在双层以及细胞中,复合物的单通道电导取决于LRRC8的组成。最后,在不存在渗透梯度的情况下,低离子强度(Gamma)会激活双层复合物。这些数据表明LRRC8蛋白一起构成了VRAC孔,低渗应激可以通过细胞质γ的降低激活VRAC。

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