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体内Ld细胞表面水平的定量分析导致2C转基因T细胞受体的阳性与阴性选择。

Quantitation of the cell surface level of Ld resulting in positive versus negative selection of the 2C transgenic T cell receptor in vivo.

作者信息

Cook J R, Wormstall E M, Hornell T, Russell J, Connolly J M, Hansen T H

机构信息

Department of Genetics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Immunity. 1997 Aug;7(2):233-41. doi: 10.1016/s1074-7613(00)80526-9.

Abstract

The 2C transgenic TCR is positively selected on Kb and is alloreactive for and negatively selected on Ld. To test an avidity model for positive selection, mice were bred to express different levels of surface Ld by varying the number of gene copies encoding beta 2-microglobulin (beta 2m) or Ld heavy chain. Whereas mice expressing 35% Ld (beta 2m+/- Ld+/-) negatively selected the 2C TCR, mice expressing 2% Ld (beta 2m-/- Ld+/-) positively selected the 2C TCR. Furthermore, 2C cytotoxic T lymphocytes selected on 2% Ld showed peptide-specific cytolytic activity against Ld/p2Ca targets. These findings provide clear in vivo evidence that positive selection can occur on very low levels of the same class I antigen capable of negative selection when expressed at higher levels.

摘要

2C转基因TCR在Kb上被阳性选择,对Ld具有同种异体反应性,并在Ld上被阴性选择。为了测试阳性选择的亲和力模型,通过改变编码β2-微球蛋白(β2m)或Ld重链的基因拷贝数,培育出表达不同水平表面Ld的小鼠。表达35%Ld(β2m+/-Ld+/-)的小鼠对2C TCR进行阴性选择,而表达2%Ld(β2m-/-Ld+/-)的小鼠对2C TCR进行阳性选择。此外,在2%Ld上选择的2C细胞毒性T淋巴细胞对Ld/p2Ca靶标表现出肽特异性溶细胞活性。这些发现提供了明确的体内证据,表明阳性选择可以在非常低水平的同一I类抗原上发生,而当该抗原以较高水平表达时能够进行阴性选择。

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