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通过抗原激活对CD4进行调节。

Modulation of CD4 by antigenic activation.

作者信息

Weyand C M, Goronzy J, Fathman C G

出版信息

J Immunol. 1987 Mar 1;138(5):1351-4.

PMID:3100638
Abstract

Cell surface expression of CD4, an invariant membrane glycoprotein, is characteristic of the MHC class II-restricted T cell helper/inducer subset. Although the specificity and restriction patterns of T lymphocytes are determined by the T cell receptor for antigen, CD4 might represent an additional "interaction" molecule that is required to strengthen the interaction between T cells, antigen, and antigen-presenting cells. In this manuscript, we have shown that the cell surface expression of CD4 is correlated with activation of T cells. Data presented in this paper have demonstrated, for the first time, that antigenic stimulation of human T cell clones caused a decrease in the expression of the CD4 marker (as well as to the CD3 marker) to about 50% of the constitutive level. As previously demonstrated, PMA caused modulation of CD4 and CD3, which suggested that phosphorylation by protein kinase C played a crucial role in the regulation of the expression of both markers. The parallel down-regulation of CD3 and CD4 after antigen stimulation suggested that both markers might be members of a multimolecular complex mediating T cell activation.

摘要

CD4是一种恒定的膜糖蛋白,其细胞表面表达是MHC II类限制性T细胞辅助/诱导亚群的特征。尽管T淋巴细胞的特异性和限制性模式由抗原的T细胞受体决定,但CD4可能代表一种额外的“相互作用”分子,它是加强T细胞、抗原和抗原呈递细胞之间相互作用所必需的。在本手稿中,我们已经表明CD4的细胞表面表达与T细胞的激活相关。本文所呈现的数据首次证明,人类T细胞克隆的抗原刺激导致CD4标志物(以及CD3标志物)的表达降低至组成水平的约50%。如先前所示,佛波酯(PMA)引起CD4和CD3的调节,这表明蛋白激酶C的磷酸化在两种标志物表达的调节中起关键作用。抗原刺激后CD3和CD4的平行下调表明这两种标志物可能是介导T细胞激活的多分子复合物的成员。

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