TY - JOUR
T1 - Vascular MMP-9/TIMP-2 and neuronal MMP-10 up-regulation in human brain after stroke: A combined laser microdissection and protein array study
AU - Cuadrado, Eloy
AU - Rosell, Anna
AU - Penalba, Anna
AU - Slevin, Mark
AU - Alvarez-Sabín, José
AU - Ortega-Aznar, Arantxa
AU - Montaner, Joan
PY - 2009/6/5
Y1 - 2009/6/5
N2 - Matrix Metalloproteinases (MMPs) play an important role in brain injury after ischemic stroke. In the present study, we aimed to assess the global expression of MMP-Family proteins in the human brain after stroke by using a combination of Searchlight Protein Array and Laser Microdissection to determine their cellular origin. This study demonstrated that MMP-1, MMP-2, MMP-3, MMP-8, MMP-9, MMP-10, MMP-13, and TIMP-1 were upregulated in the infarcted tissue compared to healthy control areas. Using laser microdissection we obtained specific neuronal and vascular populations from both infarcted and control areas. From these fractions, we showed that MMP-9 and TIMP-2 were highly produced in brain microvessels while MMP-10 was notably increased in neurons of the ischemic brain but not in healthy areas. These findings demonstrate a selective cell-dependent MMP secretion, opening the possibility of selectively targeting specific MMPs for neuroprotection or vasculoprotection following stroke. © 2009 American Chemical Society.
AB - Matrix Metalloproteinases (MMPs) play an important role in brain injury after ischemic stroke. In the present study, we aimed to assess the global expression of MMP-Family proteins in the human brain after stroke by using a combination of Searchlight Protein Array and Laser Microdissection to determine their cellular origin. This study demonstrated that MMP-1, MMP-2, MMP-3, MMP-8, MMP-9, MMP-10, MMP-13, and TIMP-1 were upregulated in the infarcted tissue compared to healthy control areas. Using laser microdissection we obtained specific neuronal and vascular populations from both infarcted and control areas. From these fractions, we showed that MMP-9 and TIMP-2 were highly produced in brain microvessels while MMP-10 was notably increased in neurons of the ischemic brain but not in healthy areas. These findings demonstrate a selective cell-dependent MMP secretion, opening the possibility of selectively targeting specific MMPs for neuroprotection or vasculoprotection following stroke. © 2009 American Chemical Society.
KW - Brain
KW - Laser microdissection
KW - Matrix metalloproteinases
KW - Neurons
KW - Protein array
KW - Stroke
KW - Vessels
U2 - 10.1021/pr801012x
DO - 10.1021/pr801012x
M3 - Article
SN - 1535-3893
VL - 8
SP - 3191
EP - 3197
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 6
ER -