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腹膜巨噬细胞的免疫原性与鸟氨酸生成的相关性。

Correlation of immunogenicity and production of ornithine by peritoneal macrophages.

作者信息

Kriegbaum H, Benninghoff B, Häcker-Shahin B, Dröge W

出版信息

J Immunol. 1987 Aug 1;139(3):899-904.

PMID:3110288
Abstract

The release of ornithine by macrophages and its correlation with their immunogenicity after treatment with various macrophage-stimulating substances were analyzed. Pristane-elicited peritoneal macrophages (PM) were found to express strong arginase activity and to release L-ornithine into the extracellular space. This activity is strongly reduced within 3 hr after treatment with tetradecanoylphorbol acetate (TPA) but not with lipopolysaccharide (LPS). Resident PM usually express little arginase activity, but this activity is markedly augmented within 24 or 48 hr after treatment with LPS. The release of ornithine by peritoneal cells (PC) (60 to 90% macrophages) was found to be correlated with their immunogenicity as determined by the in vivo immunization for a subsequent in vitro secondary cytotoxic response against minor H antigens. The immunogenicity of pristane-elicited PC is markedly stronger than that of resident PC or TPA-treated, pristane-elicited PC. Moreover, the immunogenicity of the resident PC and TPA-treated elicited PC is substantially augmented by the simultaneous injection of ornithine, whereas the immunogenicity of the untreated elicited PC is not further augmented by exogenous ornithine, indicating that the endogenous production of ornithine by the stimulating cells had a strong influence on the resulting immune response. Injection of glutathione into pristane-treated mice also reduces the ornithine production and immunogenicity of the resulting peritoneal exudate cells. The immunogenicity in this case is at least partly reconstituted by application of exogenous ornithine. Our experiments revealed no correlation between the production of ornithine and prostaglandin E2. Prostaglandin E2 production of resident and pristane-elicited PC is not markedly different and is in either case strongly augmented by TPA. Elicited or resident PM which have been incubated for several days in culture release practically no ornithine; but ornithine production can be induced again by incubation for 24 hr with LPS and to some extent also with interferon-gamma.

摘要

分析了巨噬细胞释放鸟氨酸的情况及其与用各种巨噬细胞刺激物质处理后免疫原性的相关性。发现经降植烷诱导的腹腔巨噬细胞(PM)表现出强烈的精氨酸酶活性,并将L-鸟氨酸释放到细胞外空间。在用十四酰佛波醇乙酸酯(TPA)处理后3小时内,这种活性会大幅降低,但用脂多糖(LPS)处理则不会。常驻PM通常表达很少的精氨酸酶活性,但在用LPS处理后24或48小时内,这种活性会显著增强。发现腹腔细胞(PC)(60%至90%为巨噬细胞)释放鸟氨酸的情况与其免疫原性相关,免疫原性通过体内免疫来确定,随后进行体外针对次要组织相容性抗原的二次细胞毒性反应。经降植烷诱导的PC的免疫原性明显强于常驻PC或经TPA处理的、经降植烷诱导的PC。此外,同时注射鸟氨酸可使常驻PC和经TPA处理的诱导PC的免疫原性大幅增强,而未经处理的诱导PC的免疫原性不会因外源性鸟氨酸而进一步增强,这表明刺激细胞内源性产生鸟氨酸对产生的免疫反应有很大影响。向经降植烷处理的小鼠注射谷胱甘肽也会降低所产生的腹腔渗出细胞的鸟氨酸产量和免疫原性。在这种情况下,通过应用外源性鸟氨酸可至少部分恢复免疫原性。我们的实验表明鸟氨酸的产生与前列腺素E2之间没有相关性。常驻PC和经降植烷诱导的PC产生前列腺素E2的情况没有明显差异,并且在任何一种情况下,TPA都会使其大幅增加。在培养中孵育数天的诱导或常驻PM几乎不释放鸟氨酸;但通过与LPS孵育24小时以及在一定程度上与干扰素-γ孵育,可再次诱导鸟氨酸的产生。

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