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蛋白激酶C参与人血管内皮细胞细胞间黏附分子-1(ICAM-1)表达的证据。

Evidence for involvement of protein kinase C in expression of intracellular adhesion molecule-1 (ICAM-1) by human vascular endothelial cells.

作者信息

Sung C P, Arleth A J, Nambi P

机构信息

Department of Cardiovascular Pharmacology and Renal Pharmacology, SmithKline Beecham Pharmaceuticals, King of Prussia, Pa 19406.

出版信息

Pharmacology. 1994 Mar;48(3):143-6. doi: 10.1159/000139173.

Abstract

Potent activators of protein kinase C (PKC), such as phorbol dibutyrate and octylindolactam V, stimulated expression of intercellular adhesion molecule 1 (ICAM-1) by human umbilical vein endothelial cells (HUVEC) in a concentration-dependent manner. Expression of PKC activator-induced ICAM-1 in HUVEC was inhibited by the PKC inhibitor, H-7. Furthermore, cytokine (TNF alpha, LPS)-induced ICAM-1 expression was inhibited by the potent PKC inhibitor, H-7, and not by the cAMP-dependent protein kinase (PKA) specific inhibitor, H-89. These data suggest that PKC is involved in cytokine- and inflammatory agent-induced upregulation of ICAM-1 expression in HUVEC.

摘要

蛋白激酶C(PKC)的强效激活剂,如佛波醇二丁酸酯和辛基吲哚酰胺V,可浓度依赖性地刺激人脐静脉内皮细胞(HUVEC)表达细胞间黏附分子1(ICAM-1)。PKC抑制剂H-7可抑制PKC激活剂诱导的HUVEC中ICAM-1的表达。此外,强效PKC抑制剂H-7可抑制细胞因子(TNFα、LPS)诱导的ICAM-1表达,而cAMP依赖性蛋白激酶(PKA)特异性抑制剂H-89则无此作用。这些数据表明,PKC参与了细胞因子和炎症因子诱导的HUVEC中ICAM-1表达上调。

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