Journal
BIOCHEMICAL PHARMACOLOGY
Volume 77, Issue 5, Pages 826-834Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bcp.2008.11.004
Keywords
Matrix metalloproteinase-2; Oxidative stress; Peroxynitrite; S-glutathiolation; Troponin 1
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Matrix metalloproteinase-2 (MMP-2) has emerged as a key protease in various pathologies associated with oxidative stress, including myocardial ischemia-reperfusion, heart failure or inflammation. Peroxynitrite (ONOO-), an important effector of oxidative stress, was reported to activate some full length MMP zymogens, particularly in the presence of glutathione (GSH), but whether this occurs for MMP-2 is unknown. Treating MMP-2 zymogen with ONOO- resulted in a concentration-dependent regulation of MMP-2, with 0.3-1 mu M ONOO- increasing and 30-100 mu M ONOO- attenuating enzyme activity. The enzyme's V-max also significantly increased by 1 mu M ONOO-. Comparable responses to ONOO- treatment were observed using the intracellular target of MMP-2, troponin I (TnI). GSH at 100 mu M attenuated the effects of ONOO- on MMP-2. Mass spectrometry revealed that ONOO- can oxidize and, in the presence of GSH, S-glutathiolate the MMP-2 zymogen or a synthetic peptide containing the cysteine-switch motif in the enzyme's autoinhibitory domain. These results suggest that ONOO- and GSH can modulate the activity of 72 kDa MMP-2 by modifying the cysteine residue in the autoinhibitory domain of the zymogen, a process that may be relevant to pathophysiological conditions associated with increased oxidative stress. (C) 2008 Elsevier Inc. All rights reserved.
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