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肿瘤坏死因子(TNF)表达的调控:γ干扰素增强脂多糖诱导的小鼠腹腔巨噬细胞中TNF的mRNA积累。

Regulation of tumor necrosis factor (TNF) expression: interferon-gamma enhances the accumulation of mRNA for TNF induced by lipopolysaccharide in murine peritoneal macrophages.

作者信息

Koerner T J, Adams D O, Hamilton T A

机构信息

Department of Pathology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Cell Immunol. 1987 Oct 15;109(2):437-43. doi: 10.1016/0008-8749(87)90326-1.

Abstract

The secretion of tumor necrosis factor (TNF) by macrophages is initiated by lipopolysaccharide (LPS); considerable evidence indicates that such secretion can be potentiated by interferon-gamma (IFN-gamma). The present studies show that accumulation of mRNA for tumor necrosis factor, which represents an important regulatory focus for controlling secretion of TNF, is enhanced by physiologic doses of IFN-gamma (20 units/ml of purified recombinant IFN-gamma). mRNA for TNF induced by LPS, which was maximal 2 hr after LPS was applied to the cells, was enhanced 5- to 8-fold by IFN-gamma as determined by Northern blot analysis. Interferon did not change the kinetics of accumulation but did change the dose effects of LPS in that increasing amounts of LPS led to increasing amounts of TNF mRNA in IFN-gamma-treated macrophages. IFN-gamma itself, however, did not induce expression of TNF mRNA. These studies document that IFN-gamma potentiates the cytoplasmic accumulation of mRNA for TNF induced in murine peritoneal macrophages by LPS.

摘要

巨噬细胞分泌肿瘤坏死因子(TNF)是由脂多糖(LPS)启动的;大量证据表明,这种分泌可被γ干扰素(IFN-γ)增强。目前的研究表明,肿瘤坏死因子mRNA的积累是控制TNF分泌的一个重要调节重点,生理剂量的IFN-γ(20单位/毫升纯化的重组IFN-γ)可增强其积累。用LPS处理细胞后2小时,LPS诱导的TNF mRNA达到最大值,通过Northern印迹分析确定,IFN-γ可使其增强5至8倍。干扰素并没有改变积累的动力学,但确实改变了LPS的剂量效应,即增加LPS的量会导致IFN-γ处理的巨噬细胞中TNF mRNA的量增加。然而,IFN-γ本身并不会诱导TNF mRNA的表达。这些研究证明,IFN-γ可增强LPS在小鼠腹腔巨噬细胞中诱导的TNF mRNA的细胞质积累。

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