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Involvement of STIM1 in the proteinase‐activated receptor 1‐mediated Ca 2+ influx in vascular endothelial cells
Author(s) -
Hirano Katsuya,
Hirano Mayumi,
Hanada Akiko
Publication year - 2009
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.22279
Subject(s) - thapsigargin , stim1 , thrombin , microbiology and biotechnology , orai1 , chemistry , cytosol , small interfering rna , receptor , transfection , biology , biochemistry , endoplasmic reticulum , enzyme , platelet , immunology , gene
Thrombin increases the cytosolic Ca 2+ concentrations and induces NO production by activating proteinase‐activated receptor 1 (PAR 1 ) in vascular endothelial cells. The store‐operated Ca 2+ influx is a major Ca 2+ influx pathway in non‐excitable cells including endothelial cells and it has been reported to play a role in the thrombin‐induced Ca 2+ signaling in endothelial cells. Recent studies have identified stromal interaction molecule 1 (STIM1) to function as a sensor of the store site Ca 2+ content, thereby regulating the store‐operated Ca 2+ influx. However, the functional role of STIM1 in the thrombin‐induced Ca 2+ influx and NO production in endothelial cells still remains to be elucidated. Fura‐2 and diaminorhodamine‐4M fluorometry was utilized to evaluate the thrombin‐induced changes in cytosolic Ca 2+ concentrations and NO production, respectively, in porcine aortic endothelial cells transfected with small interfering RNA (siRNA) targeted to STIM1. STIM1‐targeted siRNA suppressed the STIM1 expression and the thapsigargin‐induced Ca 2+ influx. The degree of suppression of the STIM1 expression correlated well to the degree of suppression of the Ca 2+ influx. The knockdown of STIM1 was associated with a substantial inhibition of the Ca 2+ influx and a partial reduction of the NO production induced by thrombin. The thrombin‐induced Ca 2+ influx exhibited the similar sensitivity toward the Ca 2+ influx inhibitors to that seen with the thapsigargin‐induced Ca 2+ influx. The present study provides the first evidence that STIM1 plays a critical role in the PAR 1 ‐mediated Ca 2+ influx and Ca 2+ ‐dependent component of the NO production in endothelial cells. J. Cell. Biochem. 108: 499–507, 2009. © 2009 Wiley‐Liss, Inc.