ATP depletion induces translocation of STIM1 to puncta and formation of STIM1-ORAI1 clusters: translocation and re-translocation of STIM1 does not require ATP

被引:38
作者
Chvanov, Michael [1 ]
Walsh, Ciara M. [1 ]
Haynes, Lee P. [1 ]
Voronina, Svetlana G. [1 ]
Lur, Gyorgy [1 ]
Gerasimenko, Oleg V. [1 ]
Barraclough, Roger [2 ]
Rudland, Philip S. [2 ]
Petersen, Ole H. [1 ]
Burgoyne, Robert D. [1 ]
Tepikin, Alexei V. [1 ]
机构
[1] Univ Liverpool, Dept Physiol, Sch Biomed Sci, Liverpool L69 3BX, Merseyside, England
[2] Univ Liverpool, Mol Med Res Grp, Sch Biol Sci, Liverpool L69 7ZB, Merseyside, England
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2008年 / 457卷 / 02期
基金
英国惠康基金; 英国医学研究理事会;
关键词
STIM1; ORAI1; ATP; Store-operated calcium influx; Ca2+ signals; ER calcium;
D O I
10.1007/s00424-008-0529-y
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Depletion of the endoplasmic reticulum (ER) calcium store triggers translocation of stromal interacting molecule one (STIM1) to the sub-plasmalemmal region and formation of puncta-structures in which STIM1 interacts and activates calcium channels. ATP depletion induced the formation of STIM1 puncta in PANC1, RAMA37, and HeLa cells. The sequence of events triggered by inhibition of ATP production included a rapid decline of ATP, depletion of phosphatidylinositol 4,5-bisphosphate (PI(4,5)P-2) and a slow calcium leak from the ER followed by formation of STIM1 puncta. STIM1 puncta induced by ATP depletion were co-localized with clusters of ORAI1 channels. STIM1-ORAI1 clusters that developed as a result of ATP depletion were very poor mediators of Ca2+ influx. Re-translocation of STIM1 from puncta back to the ER was observed during total ATP depletion. We can therefore conclude that STIM1 translocation and re-translocation as well as formation of STIM1-ORAI1 clusters occur in an ATP-independent fashion and under conditions of PI(4,5) P-2 depletion.
引用
收藏
页码:505 / 517
页数:13
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