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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >The cell-cell adhesion molecule carcinoembryonic antigen-related cellular adhesion molecule 1 inhibits IL-2 production and proliferation in human T cells by association with Src homology protein-1 and down-regulates IL-2 receptor.
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The cell-cell adhesion molecule carcinoembryonic antigen-related cellular adhesion molecule 1 inhibits IL-2 production and proliferation in human T cells by association with Src homology protein-1 and down-regulates IL-2 receptor.

机译:细胞-细胞粘附分子癌胚抗原相关的细胞粘附分子1通过与Src同源蛋白-1结合抑制人T细胞中IL-2的产生和增殖,并下调IL-2受体。

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摘要

The cell adhesion molecule, carcinoembryonic Ag-related cellular adhesion molecule 1, shown by others to both activate and inhibit T cell proliferation, exhibits a reciprocal relationship to IL-2R expression over the time course of activation of PBMCs, and upon Ab ligation, inhibits both the production of IL-2 and cell proliferation. Carcinoembryonic Ag-related cellular adhesion molecule 1 associates with CD3 and is found in lipid rafts of PBMCs, is phosphorylated on the immunoreceptor tyrosine-based inhibitory motifs (ITIMs) of the -4L isoform, and associates with Src homology protein-1, providing an explanation for its inhibitory activity. When the ITIM-containing -4L and non-ITIM-containing -4S isoforms are transfected into Jurkat cells that produce, but do not depend on IL-2 for growth, both IL-2 production and cell proliferation are differentially inhibited, demonstrating that the two isoforms signal via different pathways. When the two isoforms are transfected into Kit-225 cells that depend on IL-2 for growth, IL-2Rbeta and gamma, but not alpha subunits are down-regulated, and the -4L, but not the -4S isoform inhibits cell proliferation by 6-fold in an IL-2 dose-response study.
机译:细胞黏附分子,癌胚银相关的细胞黏附分子1,被其他人激活和抑制T细胞增殖,在激活PBMCs的过程中与IL-2R表达呈正相关关系,并且在Ab结扎后抑制IL-2的产生和细胞增殖。癌胚银相关的细胞粘附分子1与CD3缔合,并存在于PBMC的脂筏中,在-4L亚型的免疫受体基于酪氨酸的抑制性基序(ITIM)上被磷酸化,并与Src同源蛋白-1缔合。对其抑制活性的解释。当将含有ITIM的-4L和不含ITIM的-4S同工型转染至产生但不依赖IL-2的Jurkat细胞中时,IL-2的产生和细胞的增殖都受到了不同程度的抑制,这表明两个同工型通过不同的途径发出信号。当将这两种同工型转染到依赖IL-2进行生长的Kit-225细胞中时,IL-2Rbeta和gamma而不是α亚基被下调,而-4L而不是-4S同型抑制细胞增殖IL-2剂量反应研究的6倍。

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