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The intracellular Ca2+ channels of membrane traffic

机译:细胞膜内钙离子通道的运输

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摘要

Regulation of organellar fusion and fission by Ca2+ has emerged as a central paradigm in intracellular membrane traffic. Originally formulated for Ca2+-driven SNARE-mediated exocytosis in the presynaptic terminals, it was later expanded to explain membrane traffic in other exocytic events within the endo-lysosomal system. The list of processes and conditions that depend on the intracellular membrane traffic includes aging, antigen and lipid processing, growth factor signaling and enzyme secretion. Characterization of the ion channels that regulate intracellular membrane fusion and fission promises novel pharmacological approaches in these processes when their function becomes aberrant. The recent identification of Ca2+ permeability through the intracellular ion channels comprising the mucolipin (TRPMLs) and the two-pore channels (TPCs) families pinpoints the candidates for the Ca2+ channel that drive intracellular membrane traffic. The present review summarizes the recent developments and the current questions relevant to this topic.
机译:Ca 2 + 对细胞器融合和分裂的调控已成为细胞内膜运输的中心范式。最初是针对Ca 2 + 驱动的SNARE介导的突触前末端胞吐作用而配制的,后来被扩展以解释内溶酶体系统内其他胞外事件中的膜运输。取决于细胞内膜运输的过程和条件的列表包括衰老,抗原和脂质加工,生长因子信号传导和酶分泌。当细胞功能异常时,调节细胞内膜融合和裂变的离子通道的表征有望在这些过程中采用新颖的药理方法。 Ca 2 + 通过包括粘膜磷脂(TRPMLs)和双孔通道(TPCs)家族的细胞内离子通道的渗透性的最新发现为Ca 2 + 驱动细胞内膜运输的通道。本综述总结了与该主题有关的最新发展和当前问题。

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