Cassatella M A
Department of General Pathology, University of Verona, Italy.
Immunol Lett. 1996 Jan;49(1-2):79-82. doi: 10.1016/0165-2478(95)02484-0.
Lipopolysaccharide (LPS) is a potent inducer of macrophage inflammatory protein-1 alpha (MIP-1 alpha) production in human polymorphonuclear leukocytes (PMN), and it was recently shown that Interferon- gamma (IFN gamma) transiently inhibits MIP-1 alpha mRNA accumulation in LPS-stimulated PMN. To elucidate the molecular basis of the regulation of MIP-1 alpha gene expression in PMN, we investigated the effects of LPS and IFN gamma at both transcriptional and post-transcriptional levels. Nuclear run-on analysis revealed that LPS increases the transcription rate of the MIP-1 alpha gene, and that IFN gamma markedly inhibits the rate of MIP-1 alpha gene transcription in LPS-activated neutrophils. IFN gamma did not affect MIP-1 alpha mRNA stability in LPS-treated PMN, indicating that the cytokine does not regulate the LPS-induced MIP-1 alpha gene expression through post-transcriptional events. These results demonstrate that human neutrophils can actively transcribe the MIP-1 alpha gene, and that transcriptional inhibition is the mechanism whereby IFN gamma inhibits MIP-1 alpha gene expression in PMN.
脂多糖(LPS)是人类多形核白细胞(PMN)中巨噬细胞炎性蛋白-1α(MIP-1α)产生的有效诱导剂,最近有研究表明,干扰素-γ(IFNγ)可短暂抑制LPS刺激的PMN中MIP-1α mRNA的积累。为阐明PMN中MIP-1α基因表达调控的分子基础,我们在转录和转录后水平研究了LPS和IFNγ的作用。核转录分析显示,LPS可提高MIP-1α基因的转录速率,而IFNγ可显著抑制LPS激活的中性粒细胞中MIP-1α基因的转录速率。IFNγ对LPS处理的PMN中MIP-1α mRNA的稳定性没有影响,这表明该细胞因子不是通过转录后事件来调节LPS诱导的MIP-1α基因表达的。这些结果表明,人类中性粒细胞可以主动转录MIP-1α基因,转录抑制是IFNγ抑制PMN中MIP-1α基因表达的机制。