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大鼠局灶性脑缺血再灌注后FAP-1mRNA及其蛋白的表达变化

Changes of FAP-1 mRNA and protein expression in the penumbra of rat cortex after transient focal cerebral ischemia
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摘要 目的观察大鼠脑缺血再灌注后缺血半暗带皮质Fas相关的磷酸酯酶-1(FAP-1)mRNA及蛋白的表达变化。方法用半定量的逆转录PCR(RT-PCR)法检测缺血2h再灌注不同时间点缺血半暗带皮质内FAP-1mRNA的表达,免疫组化法检测FAP-1蛋白表达的变化。结果缺血半暗带脑皮质FAP-1 mRNA及其蛋白的表达于缺血灌注后再灌注1h开始明显上升,6h达高峰,24h显著下降。结论脑缺血再灌注后缺血半暗带皮质内FAP-1 mRNA及蛋白表达均明显增加,提示其可能参与了脑缺血后抗凋亡作用。 Objective To study the mRNA and protein levels of Fas associated phosphatase-1 ( FAP-1 ) in the penumbra of rat cortex after transient focal cerebral ischemia. Methods One hundred male Sprague-Dawley rats were subjected to the left middle cerebral artery occlusion for two hours, then killed at 1,3,6,12 and 24h after reperfusion. The mRNA level of FAP-1 was observed by half-quantitative RT-PCR. The protein level of FAP-1 was measured with meathod of immunohistochemistry. Results The mRNA and protein levels of FAP-1 in the penumbra of rat cortex were all increased at lh after ischemia,and peaked at 6h after reperfusion (P 〈 0. 01 ), and then markedly declined at 24h after reperfusion. Conclusion The mRNA and protein levels of FAP-1 increase in the penumbra of rat cortex after transient focal cerebral ischemia which suggests that FAP-1 may inhibit neuronal apoptosis following cerebral ischemia.
出处 《中风与神经疾病杂志》 CAS CSCD 北大核心 2009年第1期8-10,共3页 Journal of Apoplexy and Nervous Diseases
基金 国家自然科学基金资助项目(No.30370514)
关键词 脑缺血 Fas相关的磷酸酯酶-1 Cerebral ischemia Fas associated phosphatase-1
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  • 1Sen S. Programmed cell death : concept, mechanism and control [ J ]. Biol Rev Camb Philos Soc, 1992,67 (3) :287-319. 被引量:1
  • 2Sato T,Irie S, Kitada S, et al. FAP-1 :a protein tyrosine phosphatase that associates with Fas[J]. Science,1995,268(5209) :411-415. 被引量:1
  • 3Ivanov VN,Lopez Bergami P,Maulit G,et al. FAP-1 association with Fas ( Apo-1 ) inhibits Fas expression on the cell surface [ J ]. Mol Cell Biol, 2003,23 ( 10 ) : 3623-3635. 被引量:1
  • 4Longa EZ, Weinstein PR, Carlson S, et al. Reversible middle cerebral artery occlusion without craniectomy in rats [ J ]. Stroke, 1989,20 (1) :84-91. 被引量:1
  • 5Maekawa K, Imagawa N, Nagamatsu M, et al. Molecular cloning of a novel protein-tyrosine phosphatase containing a membrane-binding domain and GLGF repeats [ J ]. FEBS Lett, 1994,337:200-206. 被引量:1
  • 6Yanagisawa J, Takahashi M, Kanki H, et al. The molecular interaction of Fas and FAP-1 : A tripepide blocker of human Fas interaction with FAP-1 promotes Fas-induced apoptosis [ J]. Biol Chem, 1997,272 (13) :8539-8545. 被引量:1
  • 7Irie S, Hachiya T, Rabizadeh S, et al. Functional interaction of Fas-associated phosphatase-1 ( FAP-1 ) with p75 ( NTR ) and their effect on NF-kappaB activation[ J]. FEBS Lett, 1999,460 (2) : 191-198. 被引量:1
  • 8Li Y, Kanki H, Hachiya T, et al. Negative regulation of Fas-mediated apoptosis by FAP-1 in human cancer cells[ J]. Int J Cancer,2000,87 (4) :473-479. 被引量:1
  • 9周伟,吴圣楣,陈惠金,陆良勇.运用原位末端标记技术检测大鼠缺氧缺血性脑损伤中III型细胞死亡[J].中华儿科杂志,2000,38(4):228-230. 被引量:6

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