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用针对p42和p44丝裂原活化蛋白激酶的反义硫代磷酸酯寡脱氧核苷酸处理血管平滑肌细胞,可消除对血小板衍生生长因子的DNA合成反应。

Treatment of vascular smooth muscle cells with antisense phosphorothioate oligodeoxynucleotides directed against p42 and p44 mitogen-activated protein kinases abolishes DNA synthesis in response to platelet-derived growth factor.

作者信息

Robinson C J, Scott P H, Allan A B, Jess T, Gould G W, Plevin R

机构信息

Department of Physiology and Pharmacology, University of Strathclyde, Royal College, Glasgow, U.K.

出版信息

Biochem J. 1996 Nov 15;320 ( Pt 1)(Pt 1):123-7. doi: 10.1042/bj3200123.

Abstract

We have investigated the requirement for mitogen-activated protein (MAP) kinase in the stimulation of DNA synthesis by platelet-derived growth factor (PDGF) in rat aortic smooth muscle cells using a phosphorothioate-modified oligodeoxy-nucleotide (ODN) to deplete MAP kinase. Treatment for 72 h with MAP kinase antisense ODN directed against both the p42 and p44 isoforms of MAP kinase abolished the expression of MAP kinase and reduced agonist-stimulated MAP kinase activity by approx. 95%. The scrambled control ODN was without effect, but the sense control ODN slightly enhanced the expression of both isoforms. Abolition of MAP kinase activity by antisense ODN treatment prevented angiotensin II- and PDGF-stimulated activation of p90 ribosomal S6 kinase activity, but did not affect activation of MAP kinase kinase. In addition, antisense ODN pretreatment reduced PDGF-stimulated [3H]thymidine incorporation to < 5% of control, and decreased basal incorporation by approx. 90%. In contrast, basal [3H]thymidine incorporation was enhanced approx. 60% by control sense ODN treatment. These results indicate an obligatory role for MAP kinase in the activation of a number of early events in mitogenesis, including DNA synthesis, in vascular smooth muscle cells.

摘要

我们使用硫代磷酸酯修饰的寡脱氧核苷酸(ODN)来消耗丝裂原活化蛋白(MAP)激酶,研究了大鼠主动脉平滑肌细胞中血小板衍生生长因子(PDGF)刺激DNA合成时对MAP激酶的需求。用针对MAP激酶的p42和p44亚型的MAP激酶反义ODN处理72小时,可消除MAP激酶的表达,并使激动剂刺激的MAP激酶活性降低约95%。乱序对照ODN无效,但正义对照ODN略微增强了两种亚型的表达。反义ODN处理消除MAP激酶活性可阻止血管紧张素II和PDGF刺激的p90核糖体S6激酶活性的激活,但不影响MAP激酶激酶的激活。此外,反义ODN预处理可将PDGF刺激的[3H]胸苷掺入量降低至对照的<5%,并使基础掺入量降低约90%。相比之下,对照正义ODN处理可使基础[3H]胸苷掺入量增加约60%。这些结果表明,MAP激酶在血管平滑肌细胞有丝分裂的许多早期事件(包括DNA合成)的激活中起关键作用。

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