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Influence of CD80 and CD86 Co-Stimulation in the Modulation of the Activation of Antigen Presenting Cells

机译:CD80和CD86共刺激对抗原呈递细胞激活的调节作用

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The role of CD80 and CD86 costimulatory molecules is well established in the activation of T cells but not antigen presenting cells. Recently, many reports in literature have demonstrated categorically the influence of CD80 and CD86 in the activation of B cells and dendritic cells. Stimulation via CD80/CD86 in B cells can modulate their proliferation, IgG secretion and expression of pro-apoptotic and anti-apoptotic molecules, nuclear localization of NF-κB p50 subunit, phosphorylation of Rel A (p65) and IκB-alpha and increased oct-2 expression. In case of dendritic cells, it has been shown that signals induced via CD80 and CD86 enhance the production of IL-6 and IFN-γ which in turn, upregulates the expression of the enzyme indolamine 2, 3-dioxygenase that results in tryptophan catabolism and affects T cell proliferation. Interestingly, it has been shown that co-stimulation through CD80 can restrict the survival of lymphomas and can also induce apoptosis in neural stem cells. Consequently, it may be concluded that CD28/CD152-CD80/86 interaction delivers a bi-directional co-stimulation, thereby not only having impact on the function of T cells, but also antigen presenting cells.
机译:CD80和CD86共刺激分子的作用在T细胞而非抗原呈递细胞的活化中得到了很好的确立。近来,许多文献报道已经明确地证明了CD80和CD86对B细胞和树突状细胞的活化的影响。通过B细胞中CD80 / CD86的刺激可以调节其增殖,IgG分泌以及促凋亡和抗凋亡分子的表达,NF-κBp50亚基的核定位,Rel A(p65)和IκB-alpha的磷酸化以及增加的oct -2表达式。对于树突状细胞,已经证明通过CD80和CD86诱导的信号增强了IL-6和IFN-γ的产生,进而上调了吲哚胺2、3-双加氧酶的表达,导致色氨酸分解代谢和影响T细胞增殖。有趣的是,已经表明通过CD80的共同刺激可以限制淋巴瘤的存活,还可以诱导神经干细胞凋亡。因此,可以得出结论,CD28 / CD152-CD80 / 86相互作用提供了双向共刺激,从而不仅对T细胞的功能有影响,而且对抗原呈递细胞也有影响。

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