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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。

相似文献

1
Kinetics of the biosynthesis of complement subcomponent C1q by murine macrophages: effects of stimulation by interferon-gamma.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。
J Interferon Res. 1991 Apr;11(2):111-9.
2
Kinetics of the biosynthesis of complement subcomponent C1q by murine macrophages: LPS, immune complexes, and zymosan alone and in combination with interferon-gamma.小鼠巨噬细胞合成补体亚成分C1q的动力学:脂多糖、免疫复合物、酵母聚糖单独及与γ干扰素联合作用的情况
J Leukoc Biol. 1991 Nov;50(5):453-63. doi: 10.1002/jlb.50.5.453.
3
Inhibitors of C1q biosynthesis suppress activation of murine macrophages for both antibody-independent and antibody-dependent tumor cytotoxicity.C1q生物合成抑制剂可抑制鼠巨噬细胞的激活,从而抑制抗体非依赖型和抗体依赖型肿瘤细胞毒性。
J Immunol. 1990 Mar 15;144(6):2281-6.
4
Reconstitution of a deficiency of AKR mouse macrophages for their response to lipid A activation for tumor cytotoxicity by complement subcomponent C1q: role of IFN-gamma.通过补体亚成分C1q重建AKR小鼠巨噬细胞对脂多糖激活的肿瘤细胞毒性反应的缺陷:γ干扰素的作用
J Immunol. 1991 Aug 15;147(4):1315-21.
5
Stimulation of macrophage synthesis of complement C1q by interferon-gamma mediated by endogenous interferon-alpha/beta.内源性干扰素α/β介导的干扰素γ刺激巨噬细胞合成补体C1q。
J Interferon Cytokine Res. 1996 Mar;16(3):245-9. doi: 10.1089/jir.1996.16.245.
6
Autocrine induction of macrophage synthesis of complement subcomponent C1q by endogenous interferon-alpha/beta.内源性干扰素-α/β对巨噬细胞合成补体亚成分C1q的自分泌诱导作用。
J Interferon Cytokine Res. 1996 Mar;16(3):209-15. doi: 10.1089/jir.1996.16.209.
7
Exogenous C1q reconstitutes a secondary deficiency of C5-deficient AKR mouse macrophages for FcR-dependent cellular cytotoxicity and phagocytosis.外源性C1q可重建C5缺陷型AKR小鼠巨噬细胞因FcR依赖性细胞毒性和吞噬作用而产生的继发性缺陷。
J Immunol. 1991 Feb 15;146(4):1233-9.
8
Evidence for endogenous C1q modulates TNF-alpha receptor synthesis and autocrine binding of TNF-alpha associated with lipid A activation of murine macrophages for nitric oxide production.内源性C1q的证据调节肿瘤坏死因子-α受体合成以及与脂多糖激活小鼠巨噬细胞产生一氧化氮相关的肿瘤坏死因子-α的自分泌结合。
Cell Immunol. 1996 May 25;170(1):34-40. doi: 10.1006/cimm.1996.0131.
9
Elevation by muroctasin of the serum level of the complement subcomponent C1q in mice and of its biosynthesis by cultured mouse peritoneal macrophages.香菇多糖对小鼠血清补体亚成分C1q水平及其在培养的小鼠腹腔巨噬细胞中生物合成的提升作用。
Arzneimittelforschung. 1990 Jan;40(1):58-61.
10
Exogenous C1q reconstitutes resident but not inflammatory mouse peritoneal macrophages for Fc receptor-dependent cellular cytotoxicity and phagocytosis. Relationship to endogenous C1q availability.外源性C1q可重构驻留而非炎性小鼠腹腔巨噬细胞,以实现Fc受体依赖性细胞毒性和吞噬作用。与内源性C1q可用性的关系。
J Immunol. 1989 Nov 15;143(10):3250-7.

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