S-Nitrosylation of Matrix Metalloproteinases: Signaling Pathway to Neuronal Cell Death

Zezong Gu(Sanford Burnham Prebys Medical Discovery Institute), Marcus Kaul, Boxu Yan(Sanford Burnham Prebys Medical Discovery Institute), Steven J. Kridel(Sanford Burnham Prebys Medical Discovery Institute), Jiankun Cui, Alex Y. Strongin(Sanford Burnham Prebys Medical Discovery Institute), Jeffrey W. Smith(Sanford Burnham Prebys Medical Discovery Institute), Robert Liddington(Sanford Burnham Prebys Medical Discovery Institute), Stuart A. Lipton
Science
August 16, 2002
Cited by 948

Abstract

Matrix metalloproteinases (MMPs) are implicated in the pathogenesis of neurodegenerative diseases and stroke. However, the mechanism of MMP activation remains unclear. We report that MMP activation involves S-nitrosylation. During cerebral ischemia in vivo, MMP-9 colocalized with neuronal nitric oxide synthase. S-Nitrosylation activated MMP-9 in vitro and induced neuronal apoptosis. Mass spectrometry identified the active derivative of MMP-9, both in vitro and in vivo, as a stable sulfinic or sulfonic acid, whose formation was triggered by S-nitrosylation. These findings suggest a potential extracellular proteolysis pathway to neuronal cell death in which S-nitrosylation activates MMPs, and further oxidation results in a stable posttranslational modification with pathological activity.


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