Electroporation loading and photoactivation of caged InsP3:: tools to investigate the relation between cellular ATP release in response to intracellular InsP3 elevation

被引:10
作者
Braet, K
Mabilde, C
Cabooter, L
Rapp, G
Leybaert, L
机构
[1] Univ Ghent, B-9000 Ghent, Belgium
[2] Rapp OptoElect GmbH, D-22559 Hamburg, Germany
关键词
flash photolysis; electroporation; caged compounds; InsP(3); ATP release; calcium signaling; calcium waves;
D O I
10.1016/j.jneumeth.2003.09.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Photolytic liberation of InsP(3) in single cells triggers cell-to-cell propagating calcium changes that are communicated by a gap junctional and a paracrine purinergic pathway involving InsP(3)-triggered ATP release. We investigated the relation between the InsP(3) stimulus and the resulting ATP release in ECV304 cells using UV photolysis of caged compounds and bioluminescent ATP measurements. Careful consideration of all steps, starting from caged InsP(3) loading into the cells by electroporation, up to photoliberation upon UV exposure, allowed to derive a dose-response relation that revealed a first part with a flattening ATP release response in the below 10 muM InsP(3) concentration range and a second phase of steeply increasing ATP release in response to above 10 muM InsP(3) stimulation. ATP release triggered by below 10 muM InsP(3) concentrations attained a level in the order of 30% above baseline ATP release, while the steeply increasing response to high InsP(3) concentrations attained values in the order of 150% above baseline. Our data indicate the involvement of low affinity InsP(3) receptor sites in the pathway leading to triggered ATP release, with activation of these receptors causing the release of 1-2% of the total cellular ATP pool. (C) 2003 Elsevier B.V All rights reserved.
引用
收藏
页码:81 / 89
页数:9
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