Photoliberating inositol-1,4,5-trisphosphate triggers ATP release that is blocked by the connexin mimetic peptide gap 26

被引:134
作者
Braet, K
Vandamme, W
Martin, PEM
Evans, WH
Leybaert, L
机构
[1] State Univ Ghent, Dept Physiol & Pathophysiol, B-9000 Ghent, Belgium
[2] Univ Wales Coll Cardiff, Coll Med, Dept Biochem Med, Cardiff CF1 3NS, S Glam, Wales
关键词
ATP release; inositol trisphosphate; calcium signalling; flash photolysis; gap junctions; hemichannels;
D O I
10.1016/S0143-4160(02)00180-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Calcium signals can be communicated between cells by the diffusion of a second messenger through gap junction channels or by the release of an extracellular purinergic messenger. We investigated the contribution of these two pathways in endothelial cell lines by photoliberating InSP3 or calcium from intracellular caged precursors, and recording either the resulting intercellular calcium wave or else the released ATP with a luciferin/luciferase assay. Photoliberating InSP3 in a single cell within a confluent culture triggered an intercellular calcium wave, which was inhibited by the gap junction blocker alpha-glycyrrhetinic acid (alpha-GA), the connexin mimetic peptide gap 26, the purinergic inhibitors suramin, PPADS and apyrase and by purinergic receptor desensitisation. InsP(3)-triggered calcium waves were able to cross 20 mum wide cell-free zones. Photoliberating InSP3 triggered ATP release that was blocked by buffering intracellular calcium with BAPTA and by applying gap 26. Gap 26, however, did not inhibit the gap junctional coupling between the cells as measured by fluorescence recovery after photobleaching. Photoliberating calcium did not trigger intercellular calcium waves or ATP release. We conclude that InSP3-triggered ATP release through connexin hemichannels contributes to the intercellular propagation of calcium signals. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:37 / 48
页数:12
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