A highly specific inhibitor of matrix metalloproteinase-9 rescues laminin from proteolysis and neurons from apoptosis in transient focal cerebral ischemia

被引:359
作者
Gu, ZZ
Cui, J
Brown, S
Fridman, R
Mobashery, S
Strongin, AY
Lipton, SA [1 ]
机构
[1] Burnham Inst, Ctr Neurosci & Aging, La Jolla, CA 92037 USA
[2] Burnham Inst, Cell Adhes & Extracellular Matrix Biol Program, La Jolla, CA 92037 USA
[3] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[4] Wayne State Univ, Dept Pathol, Detroit, MI 48201 USA
关键词
matrix metalloproteinases; thiirane inhibitor; laminin; proteolysis; neurons; apoptosis;
D O I
10.1523/JNEUROSCI.1563-05.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuronal cell death occurs during many neurodegenerative disorders and stroke. The aberrant, excessive activity of matrix metalloproteinases (MMPs), especially MMP-9, contributes directly to neuron apoptosis and brain damage (Rosenberg et al., 1996; Asahi et al., 2001; Gu et al., 2002; Horstmann et al., 2003). We determined that MMP-9 degrades the extracellular matrix protein laminin and that this degradation induces neuronal apoptosis in a transient focal cerebral ischemia model in mice. We also determined that the highly specific thiirane gelatinase inhibitor SB-3CT blocks MMP-9 activity, including MMP-9-mediated laminin cleavage, thus rescuing neurons from apoptosis. We conclude that MMP-9 is a highly promising drug target and that SB-3CT derivatives have significant therapeutic potential in stroke patients.
引用
收藏
页码:6401 / 6408
页数:8
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