Department of Pharmacology, University of Oxford, U.K.
Biochem J. 2011 Nov 1;439(3):349-74. doi: 10.1042/BJ20110949.
Endosomes, lysosomes and lysosome-related organelles are emerging as important Ca2+ storage cellular compartments with a central role in intracellular Ca2+ signalling. Endocytosis at the plasma membrane forms endosomal vesicles which mature to late endosomes and culminate in lysosomal biogenesis. During this process, acquisition of different ion channels and transporters progressively changes the endolysosomal luminal ionic environment (e.g. pH and Ca2+) to regulate enzyme activities, membrane fusion/fission and organellar ion fluxes, and defects in these can result in disease. In the present review we focus on the physiology of the inter-related transport mechanisms of Ca2+ and H+ across endolysosomal membranes. In particular, we discuss the role of the Ca2+-mobilizing messenger NAADP (nicotinic acid adenine dinucleotide phosphate) as a major regulator of Ca2+ release from endolysosomes, and the recent discovery of an endolysosomal channel family, the TPCs (two-pore channels), as its principal intracellular targets. Recent molecular studies of endolysosomal Ca2+ physiology and its regulation by NAADP-gated TPCs are providing exciting new insights into the mechanisms of Ca2+-signal initiation that control a wide range of cellular processes and play a role in disease. These developments underscore a new central role for the endolysosomal system in cellular Ca2+ regulation and signalling.
内体、溶酶体和溶酶体相关细胞器正在成为重要的钙储存细胞区室,在细胞内钙信号转导中发挥核心作用。质膜的内吞作用形成内体小泡,这些小泡成熟为晚期内体,并最终导致溶酶体的生物发生。在这个过程中,不同的离子通道和转运体的获得逐渐改变内溶酶体腔的离子环境(例如 pH 和 Ca2+),以调节酶活性、膜融合/裂变和细胞器离子通量,这些缺陷会导致疾病。在本综述中,我们重点讨论了 Ca2+和 H+穿过内溶酶体膜的相关转运机制的生理学。特别是,我们讨论了 Ca2+动员信使 NAADP(烟酰胺腺嘌呤二核苷酸磷酸)作为内溶酶体 Ca2+释放的主要调节剂的作用,以及最近发现的内溶酶体通道家族 TPCs(双孔通道)作为其主要的细胞内靶标。内溶酶体 Ca2+生理学及其被 NAADP 门控 TPCs 调节的最新分子研究为 Ca2+信号起始的机制提供了令人兴奋的新见解,这些机制控制着广泛的细胞过程,并在疾病中发挥作用。这些发展强调了内溶酶体系统在细胞钙调节和信号转导中的新核心作用。