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Expression and activation of matrix metalloproteinase-2 and -9 in rat brain after transient focal cerebral ischemia

机译:短暂性局灶性脑缺血后大鼠脑中基质金属蛋白酶2和-9的表达和激活

摘要

Matrix metalloproteinases (MMPs) degrade the extracellular matrix and carry out key functions during development and after injury. By means of zymography, Western blot and immunohistochemistry, we studied MMP-2 (gelatinase A) and MMP-9 (gelatinase B) in rat brain after focal cerebral ischemia. The control rat brain showed constitutive MMP-2 and, to a lesser extent, MMP-9, which were mainly present as prozymogens. MMP-2 protein was located in the cell body of neurons, glia, and endothelium, whereas MMP-9 was associated to neurons and myelinated fibre tracts. Ischemia greatly increased MMP activation in two temporal waves, in the first one, MMP-9 protein was induced from 4 h to 4 days, and also a small and short-lasting increase in MMP-2 was detected at 4 h. The second wave showed a massive increase in MMP-2 protein expression and activation by day 4, which was compatible with abundant MMP-2 in reactive microglia/macrophages. Our results are compatible with progressive induction of MMP-9 proform, likely in neurons, shortly after ischemia. For MMP-2, the results suggest a discrete production immediately after reperfusion, while a very enhanced expression and activation of MMP-2 attributable to microglia/macrophages occurs on day 4, and it might contribute to the phagocytic action of these reactive cells. © 2001 Academic Press.
机译:基质金属蛋白酶(MMP)降解细胞外基质,并在发育过程中和受伤后发挥关键作用。通过酶谱,Western印迹和免疫组织化学,我们研究了局灶性脑缺血后大鼠脑中的MMP-2(明胶酶A)和MMP-9(明胶酶B)。对照大鼠的大脑显示出组成型MMP-2,而MMP-9的含量较小,它们主要以酶原的形式存在。 MMP-2蛋白位于神经元,神经胶质和内皮细胞的细胞体中,而MMP-9与神经元和髓鞘纤维束相关。缺血在两个时相波中大大增加了MMP的激活,在第一个时相中,从4 h到4天诱导了MMP-9蛋白,并且在4 h时还检测到MMP-2的少量且持续时间短的增加。第二波显示到第4天,MMP-2蛋白的表达和激活大量增加,这与反应性小胶质细胞/巨噬细胞中的大量MMP-2相容。我们的结果与缺血后不久可能在神经元中逐步诱导MMP-9形式相吻合。对于MMP-2,结果表明在再灌注后立即产生了离散的产物,而归因于小胶质细胞/巨噬细胞的MMP-2的表达和激活却大大增强,并在第4天发生,这可能有助于这些反应性细胞的吞噬作用。 ©2001年学术出版社。

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