首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Inhibitory effects of interferon on the expression of genes regulated by platelet-derived growth factor.
【2h】

Inhibitory effects of interferon on the expression of genes regulated by platelet-derived growth factor.

机译:干扰素对血小板衍生生长因子调控基因表达的抑制作用。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The G0/G1 to S transition in quiescent BALB/c 3T3 cells stimulated by serum growth factors can be specifically blocked by the administration of interferon (IFN) to the system. In the present communication, we studied whether IFN inhibits the early events in the G0/G1 phase that are initiated by the platelet-derived growth factor (PDGF). The results show that IFN inhibits most of the PDGF-mediated increase of c-myc, ornithine decarboxylase, and beta-actin mRNAs measured 3 hr after stimulation. c-fos mRNA levels are reduced by IFN as early as 20 min after exposure of the quiescent cells to PDGF. The expression of several genes that belong to the competence gene family is, therefore, inhibited by IFN and this could account for the failure of the IFN-treated cells to enter into the S phase when growth factors present in the platelet-poor plasma are added. We also report that the PDGF-mediated increase in the uptake of deoxyglucose is not impaired by IFN, thus suggesting that the early effects of IFN on gene expression do not result from inhibition of binding of PDGF to its cell-surface receptors. Unlike the direct stimulatory effect of PDGF, which is not sensitive to cycloheximide, the inhibitory effect of IFN on c-myc mRNA levels depends in part on protein synthesis. We propose that a putative product of one of the IFN-induced genes could mediate the decrease in expression of the PDGF-regulated gene family.
机译:血清生长因子刺激的静止BALB / c 3T3细胞中G0 / G1到S的转变可以通过向系统中施用干扰素(IFN)来特异性阻断。在本通讯中,我们研究了IFN是否抑制了血小板衍生生长因子(PDGF)引发的G0 / G1期早期事件。结果表明,在刺激后3小时,IFN抑制了大多数PDGF介导的c-myc,鸟氨酸脱羧酶和β-肌动蛋白mRNA的增加。静止细胞暴露于PDGF后20分钟,IFN降低c-fos mRNA水平。因此,属于能力基因家族的几个基因的表达受到IFN的抑制,这可以解释当添加了贫血小板血浆中存在的生长因子时,用IFN处理的细胞无法进入S期。 。我们还报告说,IFN不会损害PDGF介导的脱氧葡萄糖摄取的增加,因此表明IFN对基因表达的早期影响不是由PDGF与其细胞表面受体的结合抑制引起的。与对环己酰亚胺不敏感的PDGF的直接刺激作用不同,IFN对c-myc mRNA水平的抑制作用部分取决于蛋白质合成。我们建议推论的干扰素诱导基因之一的产物可以介导PDGF调控基因家族的表达下降。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号