Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, U.K.
Biochem Soc Trans. 2022 Aug 31;50(4):1143-1155. doi: 10.1042/BST20220229.
In recent years, our understanding of the structure, mechanisms and functions of the endo-lysosomal TPC (two-pore channel) family have grown apace. Gated by the second messengers, NAADP and PI(3,5)P2, TPCs are an integral part of fundamental signal-transduction pathways, but their array and plasticity of cation conductances (Na+, Ca2+, H+) allow them to variously signal electrically, osmotically or chemically. Their relative tissue- and organelle-selective distribution, together with agonist-selective ion permeabilities provides a rich palette from which extracellular stimuli can choose. TPCs are emerging as mediators of immunity, cancer, metabolism, viral infectivity and neurodegeneration as this short review attests.
近年来,我们对内体溶酶体 TPC(双孔通道)家族的结构、机制和功能的理解有了飞速的发展。TPC 由第二信使 NAADP 和 PI(3,5)P2 门控,是基本信号转导途径的组成部分,但它们的阳离子电导(Na+、Ca2+、H+)的排列和可塑性使它们能够以电、渗透或化学方式进行各种信号传递。它们在组织和细胞器上的相对选择性分布,加上激动剂选择性的离子通透性,为细胞外刺激提供了丰富的选择。正如这篇简短的综述所证明的那样,TPC 正在成为免疫、癌症、代谢、病毒感染和神经退行性变的介质。