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Tnfaip8 is an essential gene for the regulation of glucocorticoid-mediated apoptosis of thymocytes.

机译:Tnfaip8是调节糖皮质激素介导的胸腺细胞凋亡的必需基因。

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Glucocorticoids have significant immunoregulatory actions on thymocytes and T cells and act by binding and activating cytosolic glucocorticoid receptors, which translocate to the nucleus and control gene expression through binding to specific response elements in target genes. Glucocorticoids promote cell death by activating an apoptotic program that requires transcriptional regulation. We set out to identify genes that are crucial to the process of glucocorticoid-mediated thymocyte apoptosis. Freshly isolated murine primary thymocytes were treated with dexamethasone, mRNA isolated and used to screen DNA microarrays. A set of candidate genes with upregulated expression was identified and selected members assayed in reconstituted fetal thymic organ culture (FTOC). Fetal liver-derived hematopoietic progenitor cells (HPCs) were infected with retroviruses expressing individual genes then used to repopulate depleted fetal thymic lobes. Reconstituted FTOCs expressing the gene Tnfaip8 were treated with dexamethasone and shown to be greatly sensitized to dexamethasone. Retrovirus-mediated RNA interference was applied to knock down Tnfaip8 expression in HPCs and these were used to reconstitute FTOCs. We observed that downregulating the expression of Tnfaip8 alone was sufficient to effectively protect thymocytes against glucocorticoid-induced apoptosis. We propose that Tnfaip8 is crucial in regulating glucocorticoid-mediated apoptosis of thymocytes.
机译:糖皮质激素对胸腺细胞和T细胞具有显着的免疫调节作用,并通过结合和激活胞浆糖皮质激素受体发挥作用,该受体转运至细胞核并通过与靶基因中的特定反应元件结合来控制基因表达。糖皮质激素通过激活需要转录调节的凋亡程序来促进细胞死亡。我们着手确定对糖皮质激素介导的胸腺细胞凋亡过程至关重要的基因。用地塞米松处理新鲜分离的鼠原代胸腺细胞,分离mRNA并用于筛选DNA微阵列。鉴定了一组表达上调的候选基因,并在重构的胎儿胸腺器官培养物(FTOC)中检测了选定的成员。用表达单个基因的逆转录病毒感染胎儿肝脏来源的造血祖细胞(HPC),然后将其用于重新填充耗尽的胎儿胸腺叶。表达表达Tnfaip8基因的FTOCs用地塞米松处理,并显示出对地塞米松高度敏感。将逆转录病毒介导的RNA干扰应用于敲低HPC中Tnfaip8的表达,并将其用于重组FTOC。我们观察到,单独下调Tnfaip8的表达足以有效保护胸腺细胞抵抗糖皮质激素诱导的细胞凋亡。我们建议Tnfaip8在调节糖皮质激素介导的胸腺细胞凋亡中至关重要。

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