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牛自然杀伤细胞(NK)和淋巴因子激活的杀伤细胞(LAK)的易感性与B淋巴母细胞变体上的I类表达无关。

Bovine NK and LAK susceptibility is independent of class I expression on B lymphoblastoid variants.

作者信息

Li W, Splitter G A

机构信息

Department of Animal Health and Biomedical Sciences, University of Wisconsin-Madison 53706.

出版信息

Vet Immunol Immunopathol. 1994 Jun;41(3-4):189-200. doi: 10.1016/0165-2427(94)90096-5.

Abstract

Numerous tumors express low or no class I molecules, resulting in their avoidance of recognition and destruction by different effector cells of the immune system. Using a parent and two MHC class I mutant cell lines, we have tested the role of MHC class I molecules in natural killer (NK) cells, lymphokine activated killer (LAK) cells and cytotoxic T lymphocytes (CTLs). Both class I expressing parent cells and class I loss mutants were insensitive to NK cell lysis as assayed, regardless of the amount of class I molecules on the target cell surface. However, LAK cells demonstrated higher cytolysis on these target cells than NK cells, suggesting different mechanisms of target cell recognition or different levels of lytic activity by these two effector cell populations. Up-regulation of class I expression on the target surface by gamma interferon (gamma-IFN) had little influence on NK and LAK susceptibility, indicating there was no correlation between class I expression and bovine NK or LAK cytolysis. However, allogeneic CTLs mediated a lytic pattern distinct from NK and LAK cells, in which target sensitivity to allogeneic CTLs correlated with the amount of class I molecules expressed on the cell surface. Additionally, effector-target cell conjugation studies demonstrated that target class I expression was not involved in NK and LAK cells binding to targets. These results demonstrate that NK and LAK cytolysis of these two class I mutant cell lines is independent of the amount of class I molecules expressed on the target cell surface.

摘要

许多肿瘤表达低水平或不表达I类分子,从而使其逃避免疫系统不同效应细胞的识别和破坏。我们使用一个亲本细胞系和两个MHC I类突变细胞系,测试了MHC I类分子在自然杀伤(NK)细胞、淋巴因子激活的杀伤(LAK)细胞和细胞毒性T淋巴细胞(CTL)中的作用。如检测所示,表达I类分子的亲本细胞和I类缺失突变体对NK细胞裂解均不敏感,无论靶细胞表面I类分子的数量如何。然而,LAK细胞对这些靶细胞的细胞溶解作用比NK细胞更强,这表明这两种效应细胞群体对靶细胞的识别机制不同或裂解活性水平不同。γ干扰素(γ-IFN)使靶细胞表面I类分子表达上调,对NK和LAK细胞的敏感性影响很小,这表明I类分子表达与牛NK或LAK细胞溶解之间没有相关性。然而,同种异体CTL介导的裂解模式与NK和LAK细胞不同,其中靶细胞对同种异体CTL的敏感性与细胞表面表达的I类分子数量相关。此外,效应细胞-靶细胞结合研究表明,靶细胞I类分子表达不参与NK和LAK细胞与靶细胞的结合。这些结果表明,这两个I类突变细胞系的NK和LAK细胞溶解作用与靶细胞表面表达的I类分子数量无关。

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