Differential alterations in the expression and activity of matrix metalloproteinases 2 and 9 after transient cerebral ischemia in mice

被引:69
作者
Magnoni, S
Baker, A
George, SJ
Duncan, WC
Kerr, LE
McCulloch, J
Horsburgh, K
机构
[1] Osped Maggiore Policlin, Dipartimento Anestesia & Rianimaz Terapia Intens, IRCCS, I-20122 Milan, Italy
[2] Univ Edinburgh, Fujisawa Inst Neurosci, Edinburgh EH8 9JZ, Midlothian, Scotland
[3] Univ Edinburgh, Dept Reprod & Dev Sci, Edinburgh EH16 4SB, Midlothian, Scotland
[4] Univ Bristol, Bristol Heart Inst, Bristol BS2 8HW, Avon, England
[5] Univ Glasgow, Western Infirm, Div Cardiovasc & Med Sci, Glasgow G11 6NT, Lanark, Scotland
[6] Univ Edinburgh, Div Neurosci, Edinburgh EH8 9JZ, Midlothian, Scotland
关键词
matrix metalloproteinases (MMPs); cerebral ischemia; mice; proteolytic activity;
D O I
10.1016/j.nbd.2004.07.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Abnormal expression and activity of matrix metalloproteinases (MMPs) may contribute to the pathophysiology of cerebral disease such as ischemic injury. In this study, we compared the cellular localization, expression, and activity of MMP-2 and -9 in relation to the evolution of neuronal damage 24 and 72 h after transient global ischemia. In response to ischemia, there was a generalized increase in cellular MMP-2 immunoreactivity at 24-h reperfusion (in neurons, glia and vessels) whereas at 72-h reperfusion the increase in MMP-2 was predominantly in glia. These glial alterations contributed to a significant increase in pro MMP-2 levels in ischemic regions (P < 0.01) as measured by zymography. In contrast, MMP-9 was predominantly upregulated in neurons and this was significantly different to shams at 24- and 72-h reperfusion after ischemia (P < 0.05). Notably, a dramatic increase in proteolytic activity in neurons was observed 24 h after ischemia and this response was absent at 72 h post-ischemia. The present data are supportive of a role for MMPs in contributing to neuronal injury after ischemia. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:188 / 197
页数:10
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