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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >The molecular signature of CD8+ T cells undergoing deletional tolerance
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The molecular signature of CD8+ T cells undergoing deletional tolerance

机译:CD8 + T细胞经历缺失耐受的分子特征

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Peripheral tolerance induction is critical for the maintenance of self-tolerance and can be mediated by immunoregulatory T cells or by direct induction of T-cell anergy or deletion. Although the molecular processes underlying anergy have been extensively studied, little is known about the molecular basis for peripheral T-cell deletion. Here, we determined the gene expression signature of peripheral CD8+ T cells undergoing deletional tolerance, relative to those undergo-ing immunogenic priming or lymphopenia-induced proliferation. From these data, we report the first detailed molecular signature of cells undergoing deletion. Consistent with defective cytolysis, these cells exhibited deficiencies in granzyme up-regulation. Furthermore, they showed antigen-driven Bcl-down-regulation and early up-regulation of the proapoptotic protein Bim, consistent with the requirement of this BH-only protein for peripheral T-cell deletion. Bimup-regulation was paralleled by defective interleukin-7 receptor a (IL-7Ra) chain reex-pression, suggesting that Bim-dependent death may be triggered by loss of IL-7/IL-7R signaling. Finally, we observed parallels in molecular signatures between deletion and anergy, suggesting that these tolerance pathways may not be as molecularly distinct as previously surmised.
机译:外周耐受诱导对于维持自我耐受至关重要,可以通过免疫调节性T细胞或直接诱导T细胞无反应性或缺失来介导。尽管无能为力的分子过程已得到广泛研究,但对外周T细胞缺失的分子基础知之甚少。在这里,我们确定了相对于经历免疫原性引发或淋巴细胞减少所诱导的增殖的耐受性缺失的外周CD8 + T细胞的基因表达特征。从这些数据,我们报告了正在删除的细胞的第一个详细的分子标记。与细胞溶解不良相一致,这些细胞在粒酶上调中表现出缺陷。此外,他们显示出抗原驱动的凋亡蛋白Bim的Bcl下调和早期上调,与这种仅BH的蛋白对外周T细胞缺失的要求一致。 Bimup调节与有缺陷的白介素7受体a(IL-7Ra)链表达平行,提示Bim依赖性死亡可能是由IL-7 / IL-7R信号的丧失引起的。最后,我们观察到缺失和无能力之间的分子特征相似,表明这些耐受性途径可能不像以前推测的那样具有分子差异。

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