氯离子通道
钙
生物学中的钙
细胞生物学
HEK 293细胞
细胞内
化学
胞浆
电压依赖性钙通道
调节器
钙通道
免疫沉淀
T型钙通道
生物物理学
生物化学
生物
受体
基因
有机化学
酶
作者
Aarushi Sharma,Grace Ramena,Yufang Yin,Louis S. Premkumar,Randolph C. Elble
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2018-05-14
卷期号:13 (5): e0196512-e0196512
被引量:29
标识
DOI:10.1371/journal.pone.0196512
摘要
The Chloride Channel Accessory (CLCA) protein family was first characterized as regulators of calcium-activated chloride channel (CaCC) currents (ICaCC), but the mechanism has not been fully established. We hypothesized that CLCAs might regulate ICaCC by modulating intracellular calcium levels. In cells stably expressing human CLCA2 or vector, we found by calcium imaging that CLCA2 moderately enhanced intracellular-store release but dramatically increased store-operated entry of calcium upon cytosolic depletion. Moreover, another family member, CLCA1, produced similar effects on intracellular calcium mobilization. Co-immunoprecipitation revealed that CLCA2 interacted with the plasma membrane store-operated calcium channel ORAI-1 and the ER calcium sensor STIM-1. The effect of CLCA2 on ICaCC was tested in HEK293 stably expressing calcium-activated chloride channel TMEM16A. Co-expression of CLCA2 nearly doubled ICaCC in response to a calcium ionophore. These results unveil a new mechanism by which CLCA family members activate ICaCC and suggest a broader role in calcium-dependent processes.
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