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重组肿瘤坏死因子对小鼠巨噬细胞杀瘤活性的影响:肿瘤坏死因子与γ干扰素之间的协同作用。

Effect of recombinant tumor necrosis factor on tumoricidal activation of murine macrophages: synergism between tumor necrosis factor and gamma-interferon.

作者信息

Hori K, Ehrke M J, Mace K, Mihich E

机构信息

Grace Cancer Drug Center, Roswell Park Memorial Institute, New York State Department of Health, Buffalo 14263.

出版信息

Cancer Res. 1987 Nov 15;47(22):5868-74.

PMID:3117358
Abstract

The activation of tumoricidal murine macrophages by recombinant human tumor necrosis factor (rH-TNF) alone or in combination with recombinant murine gamma-interferon (rM-IFN-gamma) was examined. When used alone, rH-TNF (10(-1)-10(5) units/ml) did not induce macrophage tumoricidal activity against TNF-insensitive P815 mastocytoma cells. Combining rH-TNF with rM-IFN-gamma resulted in the synergistic induction of tumoricidal activity in resident peritoneal macrophages. This synergistic effect was not due to contaminating bacterial lipopolysaccharide. A comparative study using recombinant murine tumor necrosis factor (rM-TNF) showed that rM-TNF alone also could not stimulate murine macrophages and there was no significant difference between effects of rM-TNF and rH-TNF on macrophage activation in the presence of rM-IFN-gamma. In experiments comparing sequential to simultaneous exposure of macrophages to rH-TNF and rM-IFN-gamma, it was found that: (a) when macrophages are primed with rM-IFN-gamma, rH-TNF serves only as a very weak triggering signal for tumoricidal activation; and (b) marked activation is obtained only when macrophages are exposed to the two cytokines simultaneously. These results suggest that TNF has an autocrine regulatory function in concert with lymphokines in macrophage-mediated host defense against tumors.

摘要

研究了单独使用重组人肿瘤坏死因子(rH-TNF)或与重组鼠γ干扰素(rM-IFN-γ)联合使用时对杀肿瘤性鼠巨噬细胞的激活作用。单独使用时,rH-TNF(10^-1 - 10^5单位/毫升)不会诱导巨噬细胞对TNF不敏感的P815肥大细胞瘤细胞产生杀肿瘤活性。将rH-TNF与rM-IFN-γ联合使用可协同诱导驻留腹膜巨噬细胞产生杀肿瘤活性。这种协同效应并非由于污染的细菌脂多糖所致。使用重组鼠肿瘤坏死因子(rM-TNF)的比较研究表明,单独的rM-TNF也不能刺激鼠巨噬细胞,并且在存在rM-IFN-γ的情况下,rM-TNF和rH-TNF对巨噬细胞激活的作用没有显著差异。在比较巨噬细胞先后和同时暴露于rH-TNF和rM-IFN-γ的实验中,发现:(a)当巨噬细胞用rM-IFN-γ预处理时,rH-TNF仅作为杀肿瘤激活的非常弱的触发信号;(b)只有当巨噬细胞同时暴露于这两种细胞因子时才会获得显著激活。这些结果表明,在巨噬细胞介导的宿主抗肿瘤防御中,TNF与淋巴因子协同具有自分泌调节功能。

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