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Am J Physiol Heart Circ Physiol 285: H866-H874, 2003. First published April 24, 2003; doi:10.1152/ajpheart.00596.2002
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HSP70.1 and -70.3 are required for late-phase protection induced by ischemic preconditioning of mouse hearts

Craig R. Hampton,1 Akira Shimamoto,1 Christine L. Rothnie,1 Jeaneatte Griscavage-Ennis,1 Albert Chong,1 David J. Dix,2 Edward D. Verrier,1 and Timothy H. Pohlman1

1Department of Surgery, University of Washington, Seattle, Washington 98104; and 2National Health and Environmental Effects Laboratory, Office of Research and Development, United States Environmental Protection Agency, Research Triangle Park, North Carolina 27711

Submitted 25 February 2002 ; accepted in final form 22 April 2003

We investigated the role of inducible heat shock proteins 70.1 and 70.3 (HSP70.1 and HSP70.3, respectively) in myocardial ischemic preconditioning (IP) in mice. Wild-type (WT) mice and HSP70.1- and HSP70.3-null [HSP70.1/3(–/–)] mice were subjected to IP and examined 24 h later during the late phase of protection. IP significantly increased steady-state levels of HSP70.1 and HSP70.3 mRNA and expression of inducible HSP70 protein in WT myocardium. To assess protection against tissue injury, mice were subjected to 30 min of regional ischemia and 3 h of reperfusion. In WT mice, IP reduced infarct size by 43% compared with sham IP-treated mice. In contrast, IP did not reduce infarct size in HSP70.1/3(–/–) mice. Absence of inducible HSP70.1 and HSP70.3 had no effect, however, on classical or early-phase protection produced by IP, which significantly reduced infarct size in HSP70.1/3(–/–) mice. We conclude that inducible HSP70.1 and HSP70.3 are required for late-phase protection against infarction following IP in mice.

heat shock proteins; knockout mice; reperfusion injury


Address for reprint requests and other correspondence: C. R. Hampton, 1959 N.E. Pacific St., Box 356410, Univ. of Washington, Seattle, WA 98195 (E-mail: champton{at}u.washington.edu).




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