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凝血酶受体的生物学功能及在脑损伤中的双重作用 被引量:1

The biologic function of thrombase and it's double function in brain damage
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摘要 1978年,Carney和Cunningham首次鉴定凝血酶受体(thrombin receptor,TR).1991年,Vu TK等克隆了第一个TR.1994年,Coughlin等依据TR由蛋白酶水解机制激活,首次命名蛋白酶激活受体(protease-activated receptors,PAR)家族属于G蛋白偶联受体超家族.1994年,Nystedt等克隆了另一个由蛋白酶水解机制激活的受体,该受体以胰蛋白酶为底物,被命名为PAR-2,故最早得到克隆的TR也被称作PAR-1.此后Hiroaki等、Xu等分别报道了另两种TR,也都属于PAR家族,分别称为PAR-3和PAR-4.目前发现的PAR成员共有4个,分别为:PAR-1、PAR-2、PAR-3和PAR-4,其中PAR-1,PAR-3和PAR-4都是TR,而PAR-2为胰酶受体.由于"PAR"已被用于表示其他基因,故根据国际遗传学标准化命名委员会的建议,将人的PAR家族的基因依次命名为:PAR1g、PAR2g、PAR3g和PAR4g[1].凝血酶在凝血级联反应中发挥着关键作用,而且凝血酶有许多细胞外的效应,通过凝血酶影响的大多数细胞的功能是由PAR介导的[2].
出处 《中国脑血管病杂志》 CAS 2004年第9期426-429,共4页 Chinese Journal of Cerebrovascular Diseases
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同被引文献8

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  • 5Kaufmann R, Patt S, Zieger M, et al. The two-receptor system PAR-1/PAR-4 mediates alpha-thrombin-induced Ca^2 + (i) mobilization in human astrocytoma cells [ J ]. J Cancer Res Clin Oncol,2000,126 (2) : 91 - 94.
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  • 8吴家幂,杨倩,袁存国.亚低温对大鼠脑缺血再灌注后炎性反应的影响[J].中国神经免疫学和神经病学杂志,2003,10(2):116-118. 被引量:5

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