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鉴定在树突状细胞中组成性表达的糖皮质激素诱导的肿瘤坏死因子受体的一种配体。

Identification of a ligand for glucocorticoid-induced tumor necrosis factor receptor constitutively expressed in dendritic cells.

作者信息

Yu Kang-Yeol, Kim Han Soo, Song Si Young, Min Sung-Shik, Jeong Jae Jun, Youn Byung-S

机构信息

KOMED Institute for Life Science, Graduate School of Biotechnology, Korea University, Rm 640, Anam-dong, Sungbuk-ku, Seoul, South Korea.

出版信息

Biochem Biophys Res Commun. 2003 Oct 17;310(2):433-8. doi: 10.1016/j.bbrc.2003.09.024.

Abstract

Glucocorticoid-induced tumor necrosis receptor (GITR) has been implicated in regulation of T cell suppression by CD25(+)CD4(+) regulatory T cells (Tregs). We isolated a cDNA encoding GITR ligand (GITRL) from mouse endothelioma cells. When stably expressed in HEK293 cells, its specific interaction with GITR was confirmed by flow cytometry with the use of GITR-Fc. The interaction was greatly diminished by the addition of soluble GITRL. Consistent with this, soluble GITRL bound to the cell surface of the GITR-expressing HEK293 cells. Coexpression of GITR with GITRL or stimulation of the GITR-expressing cells with soluble GITRL led to activation of NF-kappaB, which was significantly reduced by anti-GITR. More importantly, GITRL was expressed by both immature and mature dendritic cells, suggesting that the interaction between GITR and GITRL may contribute to immune regulation of Tregs by dendritic cells. This isolated TNFRL represents a bona fide GITRL whose presence has been elusive until this time.

摘要

糖皮质激素诱导的肿瘤坏死因子受体(GITR)与CD25(+)CD4(+)调节性T细胞(Tregs)对T细胞抑制的调节有关。我们从小鼠内皮瘤细胞中分离出一种编码GITR配体(GITRL)的cDNA。当在HEK293细胞中稳定表达时,通过使用GITR-Fc的流式细胞术证实了其与GITR的特异性相互作用。加入可溶性GITRL后,这种相互作用大大减弱。与此一致的是,可溶性GITRL与表达GITR的HEK293细胞的细胞表面结合。GITR与GITRL共表达或用可溶性GITRL刺激表达GITR的细胞会导致NF-κB活化,而抗GITR可使其显著降低。更重要的是,未成熟和成熟的树突状细胞均表达GITRL,这表明GITR与GITRL之间的相互作用可能有助于树突状细胞对Tregs的免疫调节。这种分离出的肿瘤坏死因子受体配体代表一种真正的GITRL,其存在在此之前一直难以捉摸。

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