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Characterization of a novel mouse cDNA, ES18, involved in apoptotic cell death of T-cells.

机译:新型小鼠cDNA ES18的表征,涉及T细胞凋亡。

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Using the modified screening approach in combination with expressed sequence tags, we have identified several novel cDNAs from mouse embryonic stem (ES) cells, whose expression is tissue-restricted and/or developmentally regulated. One of the cDNAs, ES18, is preferentially expressed in lymph node and thymus, and contains noteworthy features of transcriptional regulator. The expression of ES18 transcript was selectively regulated during the apoptosis of T-cell thymoma S49.1 induced by several stimuli. Interestingly, the ES18 transcript was differently regulated in the mutually antagonistic process, between dexamethasone- and A23187-induced cell death of T-cells. Moreover, the message level of ES18 was selectively enhanced by staurosporine, a broad protein kinase inhibitor, but not by other protein kinase inhibitors such as GF109203X and H89. In addition, ES18 transcript was induced by C2-ceramide, which is a mediator of both dexamethasone- and staurosporine-induced apoptotic signaling. We further showed that transient overexpression of ES18 in mouse T-cell lymphoma increased the apoptotic cell death. These data suggest that ES18 may be selectively involved in specific apoptotic processes in mouse T-cells.
机译:使用改进的筛选方法与表达的序列标签相结合,我们从小鼠胚胎干(ES)细胞中鉴定了几种新的cDNA,它们的表达受到组织限制和/或发育调控。 cDNA之一,ES18,优先在淋巴结和胸腺中表达,并具有转录调节子的显着特征。在多种刺激诱导的T细胞胸腺瘤S49.1凋亡过程中,选择性调节ES18转录物的表达。有趣的是,在地塞米松和A23187诱导的T细胞死亡之间的相互拮抗过程中,ES18转录受到不同的调节。此外,staurosporine(一种广泛的蛋白激酶抑制剂)选择性地增强了ES18的信息水平,但没有被其他蛋白激酶抑制剂(例如GF109203X和H89)增强。另外,ES18转录物由C2-神经酰胺诱导,C2-神经酰胺是地塞米松和星形孢菌素诱导的凋亡信号传导的介体。我们进一步表明,小鼠T细胞淋巴瘤中ES18的瞬时过表达增加了凋亡细胞的死亡。这些数据表明,ES18可能选择性参与小鼠T细胞中的特定凋亡过程。

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