Sala-Rabanal Monica, Yurtsever Zeynep, Nichols Colin G, Brett Tom J
Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, United States.
Center for the Investigation of Membrane Excitability Diseases, Washington University School of Medicine, St Louis, United States.
Elife. 2015 Mar 17;4:e05875. doi: 10.7554/eLife.05875.
Calcium-activated chloride channel regulator 1 (CLCA1) activates calcium-dependent chloride currents; neither the target, nor mechanism, is known. We demonstrate that secreted CLCA1 activates calcium-dependent chloride currents in HEK293T cells in a paracrine fashion, and endogenous TMEM16A/Anoctamin1 conducts the currents. Exposure to exogenous CLCA1 increases cell surface levels of TMEM16A and cellular binding experiments indicate CLCA1 engages TMEM16A on the surface of these cells. Altogether, our data suggest that CLCA1 stabilizes TMEM16A on the cell surface, thus increasing surface expression, which results in increased calcium-dependent chloride currents. Our results identify the first Cl(-) channel target of the CLCA family of proteins and establish CLCA1 as the first secreted direct modifier of TMEM16A activity, delineating a unique mechanism to increase currents. These results suggest cooperative roles for CLCA and TMEM16 proteins in influencing the physiology of multiple tissues, and the pathology of multiple diseases, including asthma, COPD, cystic fibrosis, and certain cancers.
钙激活氯离子通道调节剂1(CLCA1)可激活钙依赖性氯离子电流;但其靶点和作用机制均未知。我们证明,分泌型CLCA1以旁分泌方式激活HEK293T细胞中的钙依赖性氯离子电流,且内源性TMEM16A/anoctamin1传导这些电流。暴露于外源性CLCA1会增加TMEM16A的细胞表面水平,细胞结合实验表明CLCA1与这些细胞表面的TMEM16A结合。总之,我们的数据表明CLCA1可稳定细胞表面的TMEM16A,从而增加其表面表达,进而导致钙依赖性氯离子电流增加。我们的研究结果确定了CLCA蛋白家族的首个氯离子通道靶点,并将CLCA1确立为TMEM16A活性的首个分泌型直接调节剂,描绘了一种增加电流的独特机制。这些结果表明CLCA和TMEM16蛋白在影响多种组织的生理学以及多种疾病(包括哮喘、慢性阻塞性肺疾病、囊性纤维化和某些癌症)的病理学方面具有协同作用。