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磷酸胆碱和鞘氨醇-1-磷酸通过一种丝裂原活化蛋白激酶(MAP激酶)依赖的机制协同刺激DNA合成。

Phosphocholine and sphingosine-1-phosphate synergistically stimulate DNA synthesis by a MAP kinase-dependent mechanism.

作者信息

Kiss Z, Mukherjee J J

机构信息

The Hormel Institute, University of Minnesota, Austin 55912, USA.

出版信息

FEBS Lett. 1997 Jul 21;412(1):197-200. doi: 10.1016/s0014-5793(97)00776-x.

Abstract

We have previously shown that in NIH 3T3 fibroblasts phosphocholine (PCho) potentiates sphingosine-1-phosphate (S1P)-induced mitogenesis. Here we report that PCho and S1P also synergistically stimulate DNA synthesis in mouse Swiss 3T3 fibroblasts and in mouse JB6 epidermal cells. The combined actions of PCho and S1P on DNA synthesis were associated with synergistic activation of the p42/p44 mitogen-activated protein (MAP) kinases. Ethanolamine (50-100 microM) further enhanced the synergistic effects of PCho and SIP on DNA synthesis but not on MAP kinase activity. The results indicate that the synergistic mitogenic effects of PCho and S1P (i) are not restricted to NIH 3T3 fibroblasts, (ii) are predominantly mediated by the MAP kinase-dependent signal transduction pathway, and (iii) are enhanced by ethanolamine via a MAP kinase-independent mechanism.

摘要

我们之前已经表明,在NIH 3T3成纤维细胞中,磷酸胆碱(PCho)可增强1-磷酸鞘氨醇(S1P)诱导的有丝分裂。在此我们报告,PCho和S1P还能协同刺激小鼠瑞士3T3成纤维细胞和小鼠JB6表皮细胞中的DNA合成。PCho和S1P对DNA合成的联合作用与p42/p44丝裂原活化蛋白(MAP)激酶的协同激活有关。乙醇胺(50 - 100微摩尔)进一步增强了PCho和SIP对DNA合成的协同作用,但对MAP激酶活性没有影响。结果表明,PCho和S1P的协同促有丝分裂作用:(i)不限于NIH 3T3成纤维细胞;(ii)主要由MAP激酶依赖性信号转导途径介导;(iii)乙醇胺通过MAP激酶非依赖性机制增强其作用。

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