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小鼠、大鼠和人类淋巴细胞对异源靶细胞的天然细胞毒性。

Natural cytotoxicity of mouse, rat, and human lymphocytes against heterologous target cells.

作者信息

Nunn M E, Herberman R B

出版信息

J Natl Cancer Inst. 1979 Apr;62(4):765-71.

PMID:285291
Abstract

Natural cell-mediated cytotoxicity by a particular subpopulation of lymphocytes [designated natural killer (NK) cells] in NIH Swiss nude and CBA/N mice, WF rats, and humans was demonstrated against tumor cells in 4-hour 51Cr release assays. In most studies, only reactivity against target cells of the homologous species was examined. In the present studies, mouse NK activity also was found against a rat lymphoma tissue culture cell line and against human tissue culture lines. Rat NK cells reacted not only against syngeneic tumor cells but also against heterologous tumor cell lines. In contrast to the heterologous NK activity in rodents, no significant NK activity of human peripheral blood lymphocytes against heterologous targets was found in the present studies. In mice and rats the effector cells that mediated the cytotoxicity against heterologous target cells were indistinguishable from NK cells, the effector cells being nonadherent and nonphagocytic. In addition, the mouse effector cells for heterologous activity as well as mouse NK cells were sensitive to repeated treatment with anti-Thy 1.2 serum plus complement. The specificities of these reactions were indicated by a cold target inhibition assay. The results indicated a sharing of specificities between homologous and heterologous tumor cells recognized by mouse and rat NK cells. In contrast, only the human cell lines were able to appreciably inhibit the cytotoxicity of human peripheral blood lymphocytes.

摘要

在4小时的51Cr释放试验中,已证明NIH瑞士裸鼠、CBA/N小鼠、WF大鼠和人类中特定淋巴细胞亚群(称为自然杀伤细胞,即NK细胞)具有天然细胞介导的细胞毒性,可作用于肿瘤细胞。在大多数研究中,仅检测了对同物种靶细胞的反应性。在本研究中,还发现小鼠NK活性可作用于大鼠淋巴瘤组织培养细胞系和人类组织培养细胞系。大鼠NK细胞不仅对同基因肿瘤细胞有反应,而且对异源肿瘤细胞系也有反应。与啮齿动物中的异源NK活性相反,在本研究中未发现人外周血淋巴细胞对异源靶细胞有明显的NK活性。在小鼠和大鼠中,介导对异源靶细胞细胞毒性的效应细胞与NK细胞无法区分,效应细胞不具有黏附性且无吞噬作用。此外,小鼠异源活性效应细胞以及小鼠NK细胞对用抗Thy 1.2血清加补体进行的重复处理敏感。这些反应的特异性通过冷靶抑制试验得以体现。结果表明,小鼠和大鼠NK细胞识别的同源和异源肿瘤细胞之间存在特异性共享。相比之下,只有人类细胞系能够显著抑制人外周血淋巴细胞的细胞毒性。

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