Osei-Owusu James, Yang Junhua, Vitery Maria Del Carmen, Qiu Zhaozhu
Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Curr Top Membr. 2018;81:177-203. doi: 10.1016/bs.ctm.2018.07.005. Epub 2018 Aug 14.
The Volume-Regulated Anion Channel (VRAC) is activated by cell swelling and plays a key role in cell volume regulation. VRAC is ubiquitously expressed in vertebrate cells and also implicated in many other physiological and cellular processes including fluid secretion, glutamate release, membrane potential regulation, cell proliferation, migration, and apoptosis. Although its biophysical properties have been well characterized, the molecular identity of VRAC remained a mystery for almost three decades. The field was transformed by recent discoveries showing that the leucine-rich repeat-containing protein 8A (LRRC8A, also named SWELL1) and its four other homologs form heteromeric VRAC channels. The composition of LRRC8 subunits determines channel properties and substrate selectivity of a large variety of different VRACs. Incorporating purified SWELL1-containing protein complexes into lipid bilayers is sufficient to reconstitute channel activities, a finding that supports the decrease in intracellular ionic strength as the mechanism of VRAC activation during cell swelling. Characterization of Swell1 knockout mice uncovers the important role of VRAC in T cell development, pancreatic β-cell glucose-stimulated insulin secretion, and adipocyte metabolic function. The ability to permeate organic osmolytes and metabolites is a major feature of VRAC. The list of VRAC substrates is expected to grow, now also including some cancer drugs and antibiotics even under non-cell swelling conditions. Therefore, a critical role of VRAC in drug resistance and cell-cell communication is emerging. This review summarizes the exciting recent progress on the structure-function relationship and physiology of VRAC and discusses key future questions to be solved.
容积调节性阴离子通道(VRAC)由细胞肿胀激活,在细胞容积调节中起关键作用。VRAC在脊椎动物细胞中广泛表达,还参与许多其他生理和细胞过程,包括液体分泌、谷氨酸释放、膜电位调节、细胞增殖、迁移和凋亡。尽管其生物物理特性已得到充分表征,但VRAC的分子身份近三十年来一直是个谜。最近的发现改变了这一领域,表明富含亮氨酸重复序列的蛋白8A(LRRC8A,也称为SWELL1)及其其他四个同源物形成异源VRAC通道。LRRC8亚基的组成决定了各种不同VRAC的通道特性和底物选择性。将纯化的含SWELL1蛋白复合物整合到脂质双层中足以重建通道活性,这一发现支持细胞肿胀期间细胞内离子强度降低作为VRAC激活机制。对Swell1基因敲除小鼠的表征揭示了VRAC在T细胞发育、胰腺β细胞葡萄糖刺激的胰岛素分泌和脂肪细胞代谢功能中的重要作用。渗透有机渗透物和代谢物的能力是VRAC的一个主要特征。即使在非细胞肿胀条件下,VRAC底物的清单预计也会增加,现在还包括一些抗癌药物和抗生素。因此,VRAC在耐药性和细胞间通讯中的关键作用正在显现。本综述总结了VRAC结构-功能关系和生理学方面最近令人兴奋的进展,并讨论了未来有待解决的关键问题。