Thöne Fabian M B, Polovitskaya Maya M, Jentsch Thomas J
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany; Graduate program of the Freie Universität Berlin, Berlin, Germany.
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Trends Biochem Sci. 2025 Aug 5. doi: 10.1016/j.tibs.2025.07.001.
Volume-regulated anion channels (VRACs) are almost ubiquitously expressed plasma membrane (PM) channels of vertebrate cells with roles in cell volume regulation and signaling. Besides conducting anions such as chloride, VRACs transport metabolites, neurotransmitters, immunomodulators, and drugs irrespective of their electrical charge. VRAC-mediated transport of these molecules has profound (patho)physiological significance. The recent identification of VRACs as heteromers of up to five different LRRC8 proteins allowed the roles of VRACs to be addressed with genetic and molecular tools. Cryogenic electron microscopy (cryo-EM) and mutagenesis yielded insights into the structure and function of VRACs, yet their activation mechanisms remain enigmatic. Here we focus on new developments and suggest that the ability of VRAC to transport metabolites and signaling molecules may be physiologically more important than its role in cell volume regulation.
容积调节性阴离子通道(VRACs)几乎在脊椎动物细胞的质膜(PM)中普遍表达,在细胞容积调节和信号传导中发挥作用。除了传导氯离子等阴离子外,VRACs还能转运代谢物、神经递质、免疫调节剂和药物,而不考虑它们的电荷。VRAC介导的这些分子的转运具有深远的(病理)生理意义。最近将VRACs鉴定为多达五种不同LRRC8蛋白的异源二聚体,使得能够用遗传和分子工具来研究VRACs的作用。低温电子显微镜(cryo-EM)和诱变技术为VRACs的结构和功能提供了见解,但其激活机制仍然不明。在这里,我们关注新的进展,并认为VRAC转运代谢物和信号分子的能力在生理上可能比其在细胞容积调节中的作用更重要。