Inhibition of Rho-ROCK signaling induces apoptotic and non-apoptotic PS exposure in cardiomyocytes via inhibition of flippase

被引:29
作者
Krijnen, Paul A. J. [1 ,6 ]
Sipkens, Jessica A. [1 ,6 ]
Molling, Johan W. [1 ]
Rauwerda, Jan A. [2 ]
Stehouwer, Coen D. A. [6 ,7 ]
Muller, Alice [3 ,6 ]
Paulus, Walter J. [3 ,6 ]
Amerongen, Geerten P. van Nieuw [3 ,6 ]
Hack, C. Erik [5 ,6 ]
Verhoeven, Arthur J. [8 ]
van Hinsbergh, Victor W. M. [3 ,6 ]
Niessen, Hans W. M. [1 ,4 ,6 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Pathol, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Vasc Surg, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Physiol, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam Med Ctr, Dept Cardiac Surg, Amsterdam, Netherlands
[5] Vrije Univ Amsterdam Med Ctr, Dept Clin Chem, Amsterdam, Netherlands
[6] ICaR VU, Amsterdam, Netherlands
[7] Acad Hosp Maastricht, Dept Internal Med, Maastricht, Netherlands
[8] Dept Blood Cell Res, Sanquin Res CLB, Amsterdam, Netherlands
关键词
Phosphatidylserine exposure; Rho proteins; Rho-associated kinase; Flippase; Y27632; H1152; PHOSPHOLIPASE A(2) BINDS; HUMAN ENDOTHELIAL-CELLS; MEMBRANE ASYMMETRY; ANNEXIN-V; PROCOAGULANT ACTIVITY; BIOLOGICAL-MEMBRANES; HUMAN-ERYTHROCYTES; SURFACE EXPOSURE; EPITHELIAL-CELLS; LIPID ASYMMETRY;
D O I
10.1016/j.yjmcc.2010.07.017
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Subsequent to myocardial infarction, cardiomyocytes within the infarcted areas and border zones expose phosphatidylserine (PS) in the outer plasma membrane leaflet (flip-flop). We showed earlier that in addition to apoptosis, this flip-flop can be reversible in cardiomyocytes. We now investigated a possible role for Rho and downstream effector Rho-associated kinase (ROCK) in the process of (reversible) PS exposure and apoptosis in cardiomyocytes. In rat cardiomyoblasts (H9c2 cells) and isolated adult ventricular rat cardiomyocytes Clostridium difficile Toxin B (TcdB), a Rho GTPase family inhibitor, C3 transferase (C3), a Rho (A,B,C) inhibitor and the ROCK inhibitors Y27632 and H1152 were used to inhibit Rho-ROCK signaling. PS exposure was assessed via flow cytometry and fluorescent digital imaging microscopy using annexin V. Akt expression and phosphorylation were analyzed via Western blot, and Akt activity was inhibited by wortmannin. The cellular concentration activated caspase 3 was determined as a measure of apoptosis, and flippase activity was assessed via flow cytometry using NBD-labeled PS. TcdB, C3, Y27632 and H1152 all significantly increased PS exposure. TcdB, Y27632 and H1152 all significantly inhibited phosphorylation of the anti-apoptotic protein Akt and Akt inhibition by wortmannin lead to increased PS exposure. However, only TcdB and C3, but not ROCK- or Akt inhibition led to caspase 3 activation and thus apoptosis. Notably, pancaspase inhibitor zVAD only partially inhibited TcdB-induced PS exposure indicating the existence of apoptotic and non-apoptotic PS exposure. The induced PS exposure coincided with decreased flippase activity as measured with NBD-labeled PS flip-flop. In this study, we show a regulatory role for a novel signaling route, Rho-ROCK-flippase signaling, in maintaining asymmetrical membrane phospholipid distribution in cardiomyocytes. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:781 / 790
页数:10
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