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Am J Physiol Heart Circ Physiol 280: H1434-H1441, 2001;
0363-6135/01 $5.00
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Vol. 280, Issue 4, H1434-H1441, April 2001

INVITED REVIEW
Use of functional proteomics to investigate PKCepsilon -mediated cardioprotection: the signaling module hypothesis

Thomas M. Vondriska1,2, Jon B. Klein2,3,4, and Peipei Ping1,2

1 Department of Physiology and Biophysics, 2 Department of Medicine/Division of Cardiology and Division of Nephrology, 3 Department of Biochemistry, 4 Core Proteomics Laboratory at University of Louisville and Department of Veterans Affairs, and the Jewish Hospital Heart and Lung Institute, Louisville, Kentucky 40202-1783

The characterization of biological processes on the basis of alterations in the cellular proteins, or "proteomic" analysis, is a powerful approach that may be adopted to decipher the signaling mechanisms that underlie various pathophysiological conditions, such as ischemic heart disease. This review represents a prospectus for the implementation of proteomic analyses to delineate the myocardial intracellular signaling events that evoke cardioprotection against ischemic injury. In concert with this, the manifestation of a protective phenotype has recently been shown to involve dynamic modulation of protein kinase C-epsilon (PKCepsilon ) signaling complexes (Ping P, Zhang J, Pierce WM Jr, and Bolli R. Circ Res 88: 59-62, 2001). Accordingly, "the signaling module hypothesis" is formulated as a plausible mechanism by which multipurpose stress-activated proteins and signaling kinases may function collectively to facilitate the genesis of cardioprotection.

heart; protein kinase C; preconditioning; protein kinases; signaling


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