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Blood, 15 September 2006, Vol. 108, No. 6, pp. 1868-1876.
Prepublished online as a Blood First Edition Paper on May 23, 2006; DOI 10.1182/blood-2006-04-014175.
Previous Article | Next Article 
Submitted December 21, 2005
Accepted April 28, 2006
Thrombin-induced endothelial microparticle generation:
Identification of a novel pathway involving ROCK-II
activation by caspase-2
Cedric Sapet, Stephanie Simoncini, Beatrice Loriod, Denis Puthier, Jose Sampol, Catherine Nguyen, Francoise Dignat-George, and Francine ANFOSSO*
Universite Mediterranee, INSERM UMR 608
Universite Mediterranee, ERM 206 TAGC
* Corresponding author; email: anfosso{at}pharmacie.univ-mrs.fr.
Thrombin exerts pleiotropic effects on endothelial cells including the release of microparticles (EMP) that disseminate and exchange informations with vascular cells. Nevertheless, the mechanisms leading to their generation are not elucidated. We performed microarray analysis to identify genes involved in EMP release by the endothelial cell line HMEC-1 in response to thrombin. We identified a group of genes linked to the cytoskeleton reorganization family. Among these, the Rho-kinase ROCK-II presented a high transcription rate. ROCK-I, another Rho-kinase isoform, was not modulated by thrombin. Pharmacological inhibition of Rho-kinases or specific depletion of ROCK-II by short interfering (si)RNA inhibited thrombin-induced EPM release. In contrast, ROCK-I mRNA silencing did not modify EMP generation by thrombin. Exposure of HMEC-1 to thrombin in presence of the caspase-2 selective inhibitor Z-VDVAD-FMK, prevented ROCK-II cleavage and inhibited the thrombininduced EMP release. These events were observed in absence of cell death. Our data clearly identified ROCK-II as a target of thrombin in EMP generation. They indicated that the two Rho-kinases did not share identical functions. The involvement of caspase-2 in ROCK-II activation independently of cell death, points out a novel signaling pathway that emphasizes the proteolytic activity of caspase in EMP generation in response to cell activation.

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