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在缺乏TCRβ链表达的情况下,CD3ε介导的信号拯救了RAG-2-/-小鼠中CD4+CD8+胸腺细胞的发育。

CD3 epsilon-mediated signals rescue the development of CD4+CD8+ thymocytes in RAG-2-/- mice in the absence of TCR beta chain expression.

作者信息

Shinkai Y, Alt F W

机构信息

Howard Hughes Medical Institute, Boston, MA.

出版信息

Int Immunol. 1994 Jul;6(7):995-1001. doi: 10.1093/intimm/6.7.995.

Abstract

Recent studies have shown that TCR beta chain expression can effect the differentiation of CD4-CD8- double-negative (DN) thymocytes to CD4+CD8+ double-positive (DP) thymocytes. The TCR beta chain is expressed on the surface of DP thymocytes in association with CD3 gamma, delta and epsilon chains, suggesting a potential role for CD3 components in this signaling process. We now report detection of a very low level of surface expression of CD3 epsilon on adult DN RAG-2-/- thymocytes. This surface CD3 epsilon was associated with CD3 gamma and delta chains, as detected by anti-CD3 epsilon immunoprecipitation analyses. Significantly, injection of anti-CD3 epsilon mAb into RAG-2-/- mice led to the accumulation of an IL-2R alpha- CD2+ DP cell population and a nearly 100-fold increase in thymic cellularity to essentially normal levels. Together, these data strongly indicate that TCR beta chain-mediated developmental signals are transduced by CD3 components and provide potential insights into mechanisms by which TCR beta chain expression may effect this process.

摘要

最近的研究表明,TCRβ链的表达可影响CD4-CD8-双阴性(DN)胸腺细胞向CD4+CD8+双阳性(DP)胸腺细胞的分化。TCRβ链与CD3γ、δ和ε链一起表达于DP胸腺细胞表面,提示CD3组分在这一信号传导过程中可能发挥作用。我们现在报告,在成年DN RAG-2-/-胸腺细胞上检测到极低水平的表面CD3ε表达。通过抗CD3ε免疫沉淀分析检测到,这种表面CD3ε与CD3γ和δ链相关。值得注意的是,将抗CD3ε单克隆抗体注射到RAG-2-/-小鼠体内导致IL-2Rα-CD2+ DP细胞群体积累,胸腺细胞数量增加近100倍,基本恢复到正常水平。这些数据共同有力地表明,TCRβ链介导的发育信号由CD3组分转导,并为TCRβ链表达可能影响这一过程的机制提供了潜在的见解。

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