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T 细胞中非基因组糖皮质激素(GC)信号转导的新兴途径。

Emerging pathways of non-genomic glucocorticoid (GC) signalling in T cells.

机构信息

Department of Immunology and Biotechnology, Faculty of Medicine, University of Pecs, Pecs, Hungary.

出版信息

Immunobiology. 2010 Jul;215(7):521-6. doi: 10.1016/j.imbio.2009.10.003. Epub 2009 Nov 10.

Abstract

In the last decade new glucocorticoid (GC)-signalling mechanisms have emerged. The evolving field of non-genomic GC actions was precipitated from two major directions: (i) some rapid/acute clinical GC applications could not be explained based on the relatively slowly appearing genomic GC action and (ii) accumulating evidence came to light about the discrepancy in the apoptosis sensitivity and GR expression of thymocytes and other lymphoid cell types. Herein, we attempt to sample the latest information in the field of non-genomic GC signalling in T cells, and correlate it with results from our laboratory. We discuss some aspects of the regulation of thymocyte apoptosis by GCs, paying special interest to the potential role(s) of mitochondrial GR signalling. The interplay between the T cell receptor (TcR) and glucocorticoid receptor (GR) signalling pathways is described in more detail, focusing on ZAP-70, which is a novel target of rapid GC action.

摘要

在过去的十年中,新的糖皮质激素(GC)信号机制已经出现。非基因组 GC 作用这一不断发展的领域是由两个主要方向促成的:(i)一些快速/急性临床 GC 应用不能用相对较慢出现的基因组 GC 作用来解释,(ii)越来越多的证据表明,胸腺细胞和其他淋巴细胞类型的细胞凋亡敏感性和 GR 表达存在差异。在此,我们试图采集 T 细胞中非基因组 GC 信号转导领域的最新信息,并将其与我们实验室的结果相关联。我们讨论了 GC 调节胸腺细胞凋亡的一些方面,特别关注线粒体 GR 信号转导的潜在作用。详细描述了 T 细胞受体(TcR)和糖皮质激素受体(GR)信号通路之间的相互作用,重点介绍了快速 GC 作用的新靶标 ZAP-70。

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