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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Lonomycin-induced apoptosis of thymocytes is independent of Nur77 NBRE or NurRE binding, but is accompanied by Nur77 mitochondrial targeting
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Lonomycin-induced apoptosis of thymocytes is independent of Nur77 NBRE or NurRE binding, but is accompanied by Nur77 mitochondrial targeting

机译:隆诺霉素诱导的胸腺细胞凋亡独立于Nur77 NBRE或NurRE结合,但伴随Nur77线粒体靶向

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摘要

The induction of thymocyte apoptosis through the Nur77-mediated intrinsic pathway can be of physiological importance in the clonal deletion of autoreactive thymocytes during negative selection in the thymus and/or in thymocytes undergoing oncogenic transformation. lonomycin treatment induces endogenous Nur77 expression as well as apoptosis and cytochrome c release in thymocytes. Here it is shown for the first time that in normal thymocytes undergoing apoptosis, ionomycin induces translocation of endogenous Nur77 not only to the nucleus, but also to mitochondria. Immunosuppressant FK506 inhibits Nur77 NBRE and NurRE binding activity but has no effect on thymocytes apoptosis, the subcellular localization of Nur77, or cytochrome c release. This indicates that thymocytes can undergo apoptosis through the intrinsic Nur77-mediated mitochondrial pathway and that the transactivation activity of Nur77 monomers or dimers is not necessary for thymocyte apoptosis. (C) 2007 Elsevier B.V. All rights reserved.
机译:通过Nur77介导的内在途径诱导胸腺细胞凋亡对于在胸腺和/或经历致癌性转化的胸腺细胞进行负选择期间自身反应性胸腺细胞的克隆缺失可能具有重要的生理意义。洛诺霉素治疗可诱导胸腺细胞内源性Nur77表达以及细胞凋亡和细胞色素C释放。首次显示在正常胸腺细胞发生凋亡时,离子霉素不仅诱导内源性Nur77转运至细胞核,而且也转运至线粒体。免疫抑制剂FK506抑制Nur77 NBRE和NurRE结合活性,但对胸腺细胞凋亡,Nur77的亚细胞定位或细胞色素c释放没有影响。这表明胸腺细胞可以通过内在的Nur77介导的线粒体途径进行凋亡,而Nur77单体或二聚体的反式激活对于胸腺细胞的凋亡不是必需的。 (C)2007 Elsevier B.V.保留所有权利。

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