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大鼠淋巴细胞介质对小鼠巨噬细胞的体外激活作用。

In vitro activation of mouse macrophages by rat lymphocyte mediators.

作者信息

Fidler I J, Darnell J H, Budmen M B

出版信息

J Immunol. 1976 Aug;117(2):666-73.

PMID:950467
Abstract

Macrophage-activating factors (MAF)3 were released by presensitized rat lymphocytes stimulated in vitro with the appropriate antigens. Different supernatants of presensitized rat lymphocytes specifically stimulated in vitro with several different mouse, dog, and rat tumor or normal cells were capable of rendering normal rat and mouse macrophages nonspecifically cytotoxic in vitro to their respective syngeneic tumor cells. The release of active mediators by rat lymphocytes sensitized in vivo was dependent upon immunologically specific recognition of an antigen in vitro. When rat lymphocytes were incubated in vitro with antigens unrelated to the in vivo sensitizing antigens, no release of MAF occurred. Once rat MAF was released, it activated both syngeneic (rat) and xenogeneic (mouse) macrophages to kill tumor cells in vitro. These activated marcophages destroyed all syngeneic tumor targets. Such cytotoxicity was obtained even when the cells used to elicit release of MAF were totally unrelated to the target tumor cells. The data thus demonstrated that MAF can cross strain and even species specificities and can activate macrophages to kill tumors in a nonspecific manner. The cytotoxicity mediated by in vitro activated mouse macrophages decreased with time once the macrophages were removed from MAF; and by 7 days postactivation, the macrophages were not cytotoxic. However, when incubated again with MAF, significant reactivation was observed. This suggested that activation of macrophages in vivo may be a continuous process of lymphocyte-macrophage interaction.

摘要

巨噬细胞激活因子(MAF)3由预先致敏的大鼠淋巴细胞在体外用相应抗原刺激后释放。预先致敏的大鼠淋巴细胞在体外用几种不同的小鼠、狗和大鼠肿瘤细胞或正常细胞特异性刺激后的不同上清液,能够使正常大鼠和小鼠巨噬细胞在体外对各自的同基因肿瘤细胞产生非特异性细胞毒性。体内致敏的大鼠淋巴细胞释放活性介质依赖于体外对抗原的免疫特异性识别。当大鼠淋巴细胞在体外用与体内致敏抗原无关的抗原孵育时,不会释放MAF。一旦大鼠MAF释放,它就能激活同基因(大鼠)和异种(小鼠)巨噬细胞在体外杀死肿瘤细胞。这些活化的巨噬细胞会破坏所有同基因肿瘤靶标。即使用于引发MAF释放的细胞与靶肿瘤细胞完全无关,也能获得这种细胞毒性。因此,数据表明MAF可以跨越品系甚至物种特异性,并且可以激活巨噬细胞以非特异性方式杀死肿瘤。一旦巨噬细胞与MAF分离,体外活化的小鼠巨噬细胞介导的细胞毒性会随时间降低;到激活后7天,巨噬细胞不再具有细胞毒性。然而,当再次与MAF孵育时,会观察到明显的再激活。这表明体内巨噬细胞的激活可能是淋巴细胞 - 巨噬细胞相互作用的一个持续过程。

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