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人血管平滑肌细胞上存在蛋白S受体的证据。蛋白S与人血管平滑肌细胞结合特性及促有丝分裂特性的分析。

Evidence for a protein S receptor(s) on human vascular smooth muscle cells. Analysis of the binding characteristics and mitogenic properties of protein S on human vascular smooth muscle cells.

作者信息

Benzakour O, Formstone C, Rahman S, Kanthou C, Dennehy U, Scully M F, Kakkar V V, Cooper D N

机构信息

Charter Molecular Genetics Laboratory, Thrombosis Research Institute, Chelsea, London, U.K.

出版信息

Biochem J. 1995 Jun 1;308 ( Pt 2)(Pt 2):481-5. doi: 10.1042/bj3080481.

Abstract

The presence of specific binding sites for the coagulation factor protein S (PS) on the surface of human vascular smooth muscle cells (HVSMC) is described. The binding characteristics of 125I-PS to HVSMC were studied and found to be saturable, reversible and, as described by the Hill equation, co-operative (h 1.74; Kd 0.33 nM). Autoradiographic analysis of detergent extracts of HVSMC chemically cross-linked with 125I-PS and separated by SDS/PAGE revealed radioactivity associated with two proteins with apparent molecular masses of 220 and 230 kDa respectively. The mitogenic activity of PS on HVSMC was also investigated. Protein S was shown to stimulate DNA synthesis of growth-arrested HVSMC and to support their proliferation under low-serum conditions in a sustained and dose-dependent manner.

摘要

本文描述了人血管平滑肌细胞(HVSMC)表面存在凝血因子蛋白S(PS)的特异性结合位点。研究了¹²⁵I标记的PS与HVSMC的结合特性,发现其具有饱和性、可逆性,并且根据希尔方程具有协同性(h = 1.74;Kd = 0.33 nM)。对经化学交联¹²⁵I标记的PS并通过SDS/PAGE分离的HVSMC去污剂提取物进行放射自显影分析,结果显示放射性与两种蛋白质相关,其表观分子量分别为220 kDa和230 kDa。还研究了PS对HVSMC的促有丝分裂活性。结果表明,蛋白S能刺激生长停滞的HVSMC的DNA合成,并在低血清条件下以持续且剂量依赖的方式支持其增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7d6/1136950/259163e99e75/biochemj00062-0127-a.jpg

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