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活化淋巴细胞对同种异体和异种靶细胞的细胞毒性差异。III. 体外淋巴细胞靶细胞识别的物种特异性。

Differential cytotoxicity of activated lymphocytes on allogeneic and xenogeneic target cells. III. Species specificity of lymphocyte target cell recognition in vitro.

作者信息

Stejskal V, Perlmann P

出版信息

Eur J Immunol. 1976 May;6(5):347-52. doi: 10.1002/eji.1830060509.

Abstract

Cytotoxic effector lymphocytes were produced by stimulation of human peripheral blood or mouse spleen lymphocytes with PPD, PHA or PWM in vitro. The specificity of the lymphocyte target cell interaction was studied in vitro. The specificity of the lymphocyte target cell interaction was studied by adsorption of effector cells on various target cell monolayers. The cytotoxic activity of human lymphocytes against 51Cr-labeled human or monkey target cells was reduced by prior incubation on primate monolayers while it was much less affected by incubation on rodent monolayers. Conversely the cytotoxicity of mouse lymphocytes against mouse L cells was strongly reduced by absorption on mouse or rat monolayers but significantly less by that on human monolayers. This suggests that this species-specific cytotoxicity reflects recognition by activated lymphocytes of some common surface structures present only on cells of the species of the effector cell donor, or on cells from phylogenetically closely related species. Lymphocyte-mediated cytotoxicity against xenogeneic target cells was studied after stimulation with PWM. The capacity of human lymphocytes to kill 51Cr-labeled mouse cells was reduced by adsorption on either rodent or primate monolayers. Conversely, prior incubation of mouse lymphocytes on either human or mouse monolayers led to inhibition of 51Cr release from labeled Chang cells. These results suggest that the mitogen-activated effector cells which are cytotoxic for more distantly related xenogeneic target cells have receptors for structures which are common for these cells and for target cells of the species of the lymphocyte donors.

摘要

通过在体外使用结核菌素纯蛋白衍生物(PPD)、植物血凝素(PHA)或美洲商陆有丝分裂原(PWM)刺激人外周血淋巴细胞或小鼠脾淋巴细胞来产生细胞毒性效应淋巴细胞。在体外研究淋巴细胞与靶细胞相互作用的特异性。通过将效应细胞吸附在各种靶细胞单层上来研究淋巴细胞与靶细胞相互作用的特异性。人淋巴细胞对51Cr标记的人或猴靶细胞的细胞毒性活性在灵长类单层上预先孵育后降低,而在啮齿动物单层上孵育时影响较小。相反,小鼠淋巴细胞对小鼠L细胞的细胞毒性在小鼠或大鼠单层上吸附后强烈降低,但在人单层上吸附时显著降低较少。这表明这种物种特异性细胞毒性反映了活化淋巴细胞对仅存在于效应细胞供体物种的细胞或系统发育上密切相关物种的细胞上的一些共同表面结构的识别。在用PWM刺激后研究淋巴细胞介导的对异种靶细胞的细胞毒性。人淋巴细胞杀死51Cr标记的小鼠细胞的能力在啮齿动物或灵长类单层上吸附后降低。相反,小鼠淋巴细胞在人或小鼠单层上预先孵育导致标记的Chang细胞中51Cr释放受到抑制。这些结果表明,对更远缘相关异种靶细胞具有细胞毒性的丝裂原活化效应细胞具有针对这些细胞和淋巴细胞供体物种的靶细胞共有的结构的受体。

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