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脂多糖而非γ干扰素可下调小鼠巨噬细胞中c-fms原癌基因的mRNA表达。

Lipopolysaccharide, but not IFN-gamma, down-regulates c-fms mRNA proto-oncogene expression in murine macrophages.

作者信息

Gusella G L, Ayroldi E, Espinoza-Delgado I, Varesio L

机构信息

Biological Carcinogenesis Development Program, National Cancer Institute-Frederick Cancer Research Facility, MD 21701-1013.

出版信息

J Immunol. 1990 May 1;144(9):3574-80.

PMID:2139459
Abstract

In the present study we analyzed the effects of two macrophage activators, bacterial LPS and IFN-gamma, on the expression of the c-fms proto-oncogene in the immortalized murine macrophage cell line ANA-1. ANA-1 cells constitutively expressed significant levels of c-fms mRNA. LPS stimulation induced down-regulation of the expression of c-fms mRNA. In contrast, IFN-gamma did not change c-fms expression. Combined treatment of ANA-1 with IFN-gamma plus LPS resulted in a decrease in c-fms mRNA greater than that induced by LPS alone. Nuclear runoff experiments demonstrated that the down-regulation of c-fms mRNA by LPS or LPS plus IFN-gamma was controlled at a transcriptional level. Moreover, experiments in which c-fms mRNA expression was evaluated after the block of RNA or of protein synthesis did not reveal any difference in c-fms mRNA stability in LPS-treated and in untreated cells. These results demonstrate that LPS does not affect the stability of c-fms mRNA, but it decreases the transcription of the gene.

摘要

在本研究中,我们分析了两种巨噬细胞激活剂,即细菌脂多糖(LPS)和干扰素-γ(IFN-γ),对永生化小鼠巨噬细胞系ANA-1中c-fms原癌基因表达的影响。ANA-1细胞组成性表达显著水平的c-fms mRNA。LPS刺激导致c-fms mRNA表达下调。相反,IFN-γ并未改变c-fms的表达。用IFN-γ加LPS联合处理ANA-1细胞,导致c-fms mRNA的减少幅度大于单独用LPS诱导的减少幅度。核转录实验表明,LPS或LPS加IFN-γ对c-fms mRNA的下调是在转录水平上控制的。此外,在阻断RNA或蛋白质合成后评估c-fms mRNA表达的实验未发现LPS处理细胞和未处理细胞中c-fms mRNA稳定性有任何差异。这些结果表明,LPS不影响c-fms mRNA的稳定性,但会降低该基因的转录。

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