Coupling acidic organelles with the ER through Ca2+ microdomains at membrane contact sites

被引:60
作者
Penny, Christopher J. [1 ]
Kilpatrick, Bethan S. [1 ]
Eden, Emily R. [2 ]
Patel, Sandip [1 ]
机构
[1] UCL, Dept Cell & Dev Biol, London WC1E 6BT, England
[2] UCL, Inst Ophthalmol, Dept Cell Biol, London EC1V 9EL, England
基金
英国生物技术与生命科学研究理事会;
关键词
Acidic Ca2+ stores; Lysosomes; Vacuole; Endoplasmic reticulum; NAADP; Inositol trisphosphate; Cyclic ADP-ribose; Two-pore channels; TPCN1; TPCN2; IP3; receptors; Ryanodine receptors; Membrane contact sites; CICR; Computational modelling; Ca2+ microdomain; ADENINE-DINUCLEOTIDE PHOSPHATE; RYANODINE RECEPTOR; CALCIUM-RELEASE; ENDOPLASMIC-RETICULUM; 2-PORE CHANNELS; ION-CHANNEL; INOSITOL TRISPHOSPHATE; MOBILIZES CALCIUM; NAADP TRIGGERS; PH CHANGES;
D O I
10.1016/j.ceca.2015.03.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Acidic organelles such as lysosomes serve as non-canonical Ca2+ stores. The Ca2+ mobilising messenger NAADP is thought to trigger local Ca2+ release from such stores. These events are then amplified by Ca2+ channels on canonical ER Ca2+ stores to generate physiologically relevant global Ca2+ signals. Coupling likely occurs at microdomains formed at membrane contact sites between acidic organelles and the ER. Molecular analyses and computational modelling suggest heterogeneity in the composition of these contacts and predicted Ca2+ microdomain behaviour. Conversely, acidic organelles might also locally amplify and temper ER-evoked Ca2+ signals. Ca2+ microdomains between distinct Ca2+ stores are thus likely to be integral to the genesis of complex Ca2+ signals. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:387 / 396
页数:10
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