Publication | Open Access
A Highly Specific Inhibitor of Matrix Metalloproteinase-9 Rescues Laminin from Proteolysis and Neurons from Apoptosis in Transient Focal Cerebral Ischemia
415
Citations
24
References
2005
Year
ApoptosisCell DeathNeuroinflammationExcessive ActivityDegenerative PathologyBrain InjuryNeurologyMmp-9-mediated Laminin CleavageIschemic SyndromeHighly Specific InhibitorVascular BiologyNeuroprotectionCerebral Blood FlowReperfusion InjuryPharmacologyCell BiologySb-3ct DerivativesNeurodegenerative DiseasesNeuroscienceMedicineExtracellular Matrix
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.
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