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小鼠巨噬细胞补体亚成分C1q生物合成的动力学:γ干扰素刺激的影响。

Kinetics of the biosynthesis of complement subcomponent C1q by murine macrophages: effects of stimulation by interferon-gamma.

作者信息

Zhou A Q, Herriott M J, Leu R W

机构信息

Biomedical Division-Immunology Section, Samuel Roberts Noble Foundation, Inc., Ardmore, OK 73402.

出版信息

J Interferon Res. 1991 Apr;11(2):111-9.

PMID:1908003
Abstract

The effects of interferon-gamma (IFN-gamma) on the kinetics of biosynthesis of complement subcomponent C1q by mouse inflammatory peritoneal macrophages were determined. Stimulation of macrophages with various concentrations of IFN-gamma produced a dose-dependent increase in C1q mRNA accumulation which was detected as early as 3 h and sustained through 24 h, as determined by Northern blot analysis. A corresponding early increase in the extracellular accumulation of functional C1q was detected in culture supernatants after 3-9 h stimulation of macrophages with IFN-gamma that was sustained for 24-48 h as determined by a complement hemolytic assay. Autoradiographic analysis of [35S]methionine-labeled secretory C1q confirmed the protracted dose-dependent secretion of C1q by IFN-gamma stimulated macrophages during 24-48 h of culture. Western blot analysis of macrophage lysates indicated no significant changes in endogenous C1q levels following stimulation with IFN-gamma either after 3-9 h or 24-48 h when both C1q mRNA and extracellular accumulation were at their peak. Our results indicate that IFN-gamma promotes early and protracted mRNA accumulation and secretion of C1q by macrophages without intracellular accumulation, presumably due to the rapid rate of secretion of newly synthesized C1q. It is apparent that priming of macrophages with IFN-gamma provides a rapid and abundant source of secretory C1q for potential interaction with various macrophage triggering agents which also bind C1q.

摘要

测定了干扰素-γ(IFN-γ)对小鼠炎性腹腔巨噬细胞补体亚成分C1q生物合成动力学的影响。用不同浓度的IFN-γ刺激巨噬细胞,通过Northern印迹分析确定,早在3小时就检测到C1q mRNA积累呈剂量依赖性增加,并持续至24小时。在用IFN-γ刺激巨噬细胞3 - 9小时后,在培养上清液中检测到功能性C1q的细胞外积累相应早期增加,并通过补体溶血试验确定其持续24 - 48小时。对[35S]甲硫氨酸标记的分泌型C1q进行放射自显影分析证实,在培养24 - 48小时期间,IFN-γ刺激的巨噬细胞持续呈剂量依赖性分泌C1q。对巨噬细胞裂解物进行蛋白质印迹分析表明,在用IFN-γ刺激3 - 9小时或24 - 48小时后,当C1q mRNA和细胞外积累均达到峰值时,内源性C1q水平无显著变化。我们的结果表明,IFN-γ促进巨噬细胞早期和持续的mRNA积累以及C1q的分泌,而无细胞内积累,推测这是由于新合成的C1q分泌速度较快。显然,用IFN-γ预处理巨噬细胞可为与各种也结合C1q的巨噬细胞触发剂的潜在相互作用提供快速且丰富的分泌型C1q来源。

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