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I类和II类主要组织相容性复合体(MHC)限制的细胞毒性T细胞介导的细胞溶解中蛋白质合成的差异需求

Differential requirement for protein synthesis in cytolysis mediated by class I and class II MHC-restricted cytotoxic T cells.

作者信息

Tite J P

机构信息

Department of Molecular Biology, Wellcome Biotech, Beckenham, Kent, U.K.

出版信息

Immunology. 1990 Aug;70(4):440-5.

Abstract

Antigen-specific cytolysis by major histocompatibility complex (MHC) class II-restricted cloned T-cell lines was found to be dependent on protein synthesis. Cytolysis by both polyclonal short-term and long-term class I-restricted cytotoxic T lymphocytes (CTL) was almost completely insensitive to inhibitors of protein synthesis. Kinetic studies with class II-restricted CTL indicated that approximately 2-3 hr after initiation of activation, resistance to inhibitors of protein synthesis was acquired. This strongly suggests that either a cytotoxic effector molecule or an intermediary important in the delivery of such a molecule is synthesized rapidly after activation in class II-restricted CTL, whilst class I-restricted CTL have no such requirement.

摘要

研究发现,主要组织相容性复合体(MHC)Ⅱ类分子限制性克隆T细胞系的抗原特异性细胞溶解作用依赖于蛋白质合成。多克隆短期和长期Ⅰ类分子限制性细胞毒性T淋巴细胞(CTL)的细胞溶解作用对蛋白质合成抑制剂几乎完全不敏感。对Ⅱ类分子限制性CTL的动力学研究表明,激活开始后约2 - 3小时,细胞获得了对蛋白质合成抑制剂的抗性。这有力地表明,在Ⅱ类分子限制性CTL激活后会迅速合成一种细胞毒性效应分子或在传递此类分子中起重要作用的中间体,而Ⅰ类分子限制性CTL则无此需求。

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