Vascular MMP-9/TIMP-2 and Neuronal MMP-10 Up-Regulation in Human Brain after Stroke: A Combined Laser Microdissection and Protein Array Study

被引:95
作者
Cuadrado, Eloy [1 ]
Rosell, Anna [1 ]
Penalba, Anna [1 ]
Slevin, Mark [2 ]
Alvarez-Sabin, Jose [1 ]
Ortega-Aznar, Arantxa [3 ]
Montaner, Joan [1 ]
机构
[1] Autonomous Univ Barcelona, Neurovasc Res Lab,Hosp Vall Hebron, Neurovasc Unit,Inst Recerca, Dept Neurol,Dept Internal Med, E-08035 Barcelona, Spain
[2] Manchester Metropolitan Univ, SBCHS, Manchester M15 6BH, Lancs, England
[3] Hosp Gen Valle Hebron, Neuropathol Unit, Dept Pathol, Barcelona, Spain
关键词
matrix metalloproteinases; laser microdissection; protein array; neurons; vessels; brain; stroke; FOCAL CEREBRAL-ISCHEMIA; CAPTURE MICRODISSECTION; MATRIX METALLOPROTEINASES; NEUTROPHIL INFILTRATION; BARRIER DISRUPTION; PROTEOMIC ANALYSIS; GELATINASE-B; MATRIX-METALLOPROTEINASE-9; EXPRESSION; RAT;
D O I
10.1021/pr801012x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:3191 / 3197
页数:7
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