Multiple roles for MMPs and TIMPs in cerebral ischemia

被引:408
作者
Cunningham, LA
Wetzel, M
Rosenberg, GA
机构
[1] Univ New Mexico, Sch Med, Dept Neurosci, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Sch Med, Dept Neurol, Albuquerque, NM 87131 USA
关键词
stroke; blood-brain barrier; angiogenesis; metalloproteinase neurotrophin; Fas; VEGF;
D O I
10.1002/glia.20169
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Matrix metalloproteinases (MMPs) are matrix-degrading enzymes involved in diverse homeostatic and pathological processes. Several MMPs are expressed within the CNS and serve important normal and pathological functions during development and adulthood. An early and major pathological effect of MMP activity after cerebral ischemia is opening of the blood-brain barrier (BBB). More recent work demonstrates emerging roles for MMPs and their natural inhibitors, tissue inhibitors of metalloproteinases (TIMPs), in the regulation of neuronal cell death. In addition, MMPs and TIMPs are likely to play important roles during the repair phases of cerebral ischemia, particularly during angiogenesis and reestablishment of cerebral blood flow. This review attempts to elucidate how MMPs and TIMPs may provide detrimental or beneficial actions during the injury and repair processes after cerebral ischemia. These processes will have important implications for therapies using MMP inhibitors in stroke. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:329 / 339
页数:11
相关论文
共 120 条
[1]   Blood-brain barrier disruption and matrix metalloproteinase-9 expression during, reperfusion injury - Mechanical versus embolic focal ischemia in spontaneously hypertensive rats [J].
Aoki, T ;
Sumii, T ;
Mori, T ;
Wang, XY ;
Lo, EH .
STROKE, 2002, 33 (11) :2711-2717
[2]  
APODACA G, 1990, CANCER RES, V50, P2322
[3]   GENE ENCODING A NOVEL MURINE TISSUE INHIBITOR OF METALLOPROTEINASES (TIMP), TIMP-3, IS EXPRESSED IN DEVELOPING MOUSE EPITHELIA, CARTILAGE, AND MUSCLE, AND IS LOCATED ON MOUSE CHROMOSOME-10 [J].
APTE, SS ;
HAYASHI, K ;
SELDIN, MF ;
MATTEI, MG ;
HAYASHI, M ;
OLSEN, BR .
DEVELOPMENTAL DYNAMICS, 1994, 200 (03) :177-197
[4]   CLONING OF THE CDNA-ENCODING HUMAN TISSUE INHIBITOR OF METALLOPROTEINASES-3 (TIMP-3) AND MAPPING OF THE TIMP3 GENE TO CHROMOSOME-22 [J].
APTE, SS ;
MATTEI, MG ;
OLSEN, BR .
GENOMICS, 1994, 19 (01) :86-90
[5]  
Apte SS, 1996, J BIOL CHEM, V271, P2874
[6]   THE GENE STRUCTURE OF TISSUE INHIBITOR OF METALLOPROTEINASES (TIMP)-3 AND ITS INHIBITORY ACTIVITIES DEFINE THE DISTINCT TIMP GENE FAMILY [J].
APTE, SS ;
OLSEN, BR ;
MURPHY, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14313-14318
[7]   Essential role for ERK mitogen-activated protein kinase in matrix metalloproteinase-9 regulation in rat cortical astrocytes [J].
Arai, K ;
Lee, SR ;
Lo, EH .
GLIA, 2003, 43 (03) :254-264
[8]   Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia [J].
Asahi, M ;
Wang, XY ;
Mori, T ;
Sumii, T ;
Jung, JC ;
Moskowitz, MA ;
Fini, ME ;
Lo, EH .
JOURNAL OF NEUROSCIENCE, 2001, 21 (19) :7724-7732
[9]   Role for matrix metalloproteinase 9 after focal cerebral ischemia, effects of gene knockout and enzyme inhibition with BB-94 [J].
Asahi, M ;
Asahi, K ;
Jung, JC ;
del Zoppo, GJ ;
Fini, ME ;
Lo, EH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (12) :1681-1689
[10]   Matrix metalloproteinase 2 gene knockout has no effect on acute brain injury after focal ischemia [J].
Asahi, M ;
Sumii, T ;
Fini, ME ;
Itohara, S ;
Lo, EH .
NEUROREPORT, 2001, 12 (13) :3003-3007