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[基因靶向突变小鼠的早期T细胞发育]

[Early T cell development in gene-targeted mutant mice].

作者信息

Yu Q, Chen W F

机构信息

Department of Immunology, Beijing Medical University.

出版信息

Sheng Li Ke Xue Jin Zhan. 1997 Apr;28(2):113-8.

Abstract

Early intrathymic T cell development is highly coordinated and controlled by the interaction of a variety of molecules. The development of gene targeting technology provided a valuable tool to study the function of these molecules in vivo. The analysis of TCR and CD3 gene targeted mice indicated that CD44-CD25+ is a control point in early T cell development. At this stage, the expression of pre-TCR complex (composed of pre-TCR alpha, TCR beta and CD3) and/or its combination with unknown ligand provide signals for further progression beyond the CD44-CD25+ stage. The deficiency of any component in pre-TCR complex would lead to the blockage of T cell development at early stages.

摘要

早期胸腺内T细胞发育高度协调,并受多种分子相互作用的控制。基因靶向技术的发展为在体内研究这些分子的功能提供了宝贵工具。对TCR和CD3基因靶向小鼠的分析表明,CD44-CD25+是早期T细胞发育的一个控制点。在此阶段,前TCR复合体(由前TCRα、TCRβ和CD3组成)的表达和/或其与未知配体的结合为超越CD44-CD25+阶段的进一步发育提供信号。前TCR复合体中任何一个组分的缺陷都会导致T细胞发育在早期阶段受阻。

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