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利用脂质体中的H-2Kk分析前体细胞溶解性T淋巴细胞激活的双信号要求。

Analysis of the two-signal requirement for precursor cytolytic T lymphocyte activation using H-2Kk in liposomes.

作者信息

Herrmann S H, Weinberger O, Burakoff S J, Mescher M F

出版信息

J Immunol. 1982 May;128(5):1968-74.

PMID:6801126
Abstract

Activation of primed pre-cytolytic T lymphocytes (pCTL) requires two signals: recognition of antigen (signal 1) and interaction with a nonspecific helper factor (signal 2). The two signals necessary for generation of a secondary allogeneic CTL response have been analyzed using H-2Kk in liposomes as the stimulating antigen. Use of the liposomes allows the alloantigen to be separated from responder cells after a brief exposure. Thus, the requirements for effective delivery of each signal could be studied independently. A 12-hr exposure of pCTL to alloantigen was sufficient for optimum signal 1 delivery. pCTL recognition of the antigen occurs during this time, and no requirement for adherent cells could be demonstrated. The structure of the antigen-containing liposomes affects the efficiency of pCTL triggering. Factor(s) necessary for signal 2 could be provided by supernatants from mitogen-stimulated lymphocytes. Alternatively, it could be generated with alloantigen, providing that adherent cells were present. Optimum interaction of factor(s) with pCTL, i.e., optimum delivery of signal 2, occurred only if factor(s) was present at 12 to 24 hr after interaction of pCTL with alloantigen. The results suggest that alloantigen recognition triggers pCTL to synthesize and/or express receptors for the factor(s).

摘要

预细胞溶解T淋巴细胞(pCTL)的激活需要两个信号:抗原识别(信号1)和与非特异性辅助因子的相互作用(信号2)。使用脂质体包裹的H-2Kk作为刺激抗原,分析了产生二次同种异体CTL反应所需的两个信号。脂质体的使用使得同种异体抗原在短暂暴露后可与反应细胞分离。因此,可以独立研究有效传递每个信号的要求。将pCTL暴露于同种异体抗原12小时足以实现最佳信号1传递。在此期间发生pCTL对抗原的识别,并且未证明对贴壁细胞有需求。含抗原脂质体的结构影响pCTL触发的效率。信号2所需的因子可由丝裂原刺激的淋巴细胞的上清液提供。或者,若存在贴壁细胞,也可由同种异体抗原产生。只有当因子在pCTL与同种异体抗原相互作用后12至24小时存在时,因子与pCTL的最佳相互作用(即信号2的最佳传递)才会发生。结果表明,同种异体抗原识别触发pCTL合成和/或表达该因子的受体。

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