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青年成年鼠和老年鼠局灶性皮质缺血后基质金属蛋白酶激活的比较。

Comparison of matrix metalloproteinase activation after focal cortical ischemia in young adult and aged mice.

机构信息

Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Warsaw, Poland.

出版信息

J Neurosci Res. 2012 Jan;90(1):203-12. doi: 10.1002/jnr.22715. Epub 2011 Sep 15.

Abstract

Matrix metalloproteinase (MMP) activity is implicated in the degradation of the extracellular matrix during cerebral ischemia. Although many studies have demonstrated spatiotemporal patterns of activation of gelatinases (MMP-9 and MMP-2) after ischemic stroke in young adult rodents, no data exist on MMP activity in old brains. In this study, we investigated the gelatinolytic activity in young adult (3-month-old) and aged (1-year-old) mice subjected to photothrombotic stroke. Using in situ zymography and gel zymography, we found that the basal gelatinolytic activity in the intact cerebral cortex was similar at both investigated ages. Similarly, after photothrombosis, the increased gelatinolytic response up to 7 days poststroke was the same in young and aged brains. At both ages, early activation of gelatinolysis in the ischemic core and the perilesional area was present in neuronal nuclei as revealed by colocalization of gelatinolytic product with NeuN immunostaining and DAPI. Additionally, application of specific antibodies against MMP-9 and MMP-2 revealed the increase in MMP-9 immunoreactivity in cell nuclei as early as 4 hr poststroke. No differences between young and aged mice were observed concerning the level and localization of MMP-9 immunoreactivity. The lack of age-related differences in the degree and pattern of activation of gelatinolysis after focal stroke and the lack of correspondence between the results of in situ and gel zymography suggest that extracellular proteolysis is not directly responsible for the more severe outcome of ischemic stroke in aged subjects.

摘要

基质金属蛋白酶(MMP)的活性参与了脑缺血时细胞外基质的降解。尽管许多研究已经证明了年轻成年啮齿动物缺血性卒中后明胶酶(MMP-9 和 MMP-2)的时空激活模式,但在老年大脑中,MMP 活性的数据尚不存在。在这项研究中,我们研究了年轻成年(3 个月大)和老年(1 岁)小鼠光血栓性卒中后的明胶酶活性。通过原位酶谱法和凝胶酶谱法,我们发现,在两个研究年龄,完整大脑皮质的基础明胶酶活性相似。同样,在光血栓形成后,年轻和老年大脑中的明胶酶反应增加至卒中后 7 天是相同的。在两个年龄,缺血核心和病变周围区域的早期明胶酶激活以神经元核中的明胶酶产物与 NeuN 免疫染色和 DAPI 的共定位为特征。此外,特异性 MMP-9 和 MMP-2 抗体的应用揭示了 MMP-9 免疫反应性在卒中后 4 小时内就已经增加到细胞核中。在年轻和老年小鼠之间,关于 MMP-9 免疫反应性的水平和定位没有观察到差异。在局灶性卒中后明胶酶水解的激活程度和模式方面,年龄相关差异的缺乏以及原位酶谱法和凝胶酶谱法的结果之间缺乏对应关系表明,细胞外蛋白水解并不是老年缺血性卒中更严重结果的直接原因。

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