淋巴毒素
生物
器官发生
细胞生物学
自身免疫调节因子
基质
受体
胚胎干细胞
免疫学
细胞因子
自身免疫
免疫系统
遗传学
基因
免疫组织化学
作者
Yasuhiro Mouri,Masashi Yano,Miho Shinzawa,Yusuke Shimo,Fumiko Hirota,Yumiko Nishikawa,Takuro Nii,Hiroshi Kiyonari,Takaya Abe,Hisanori Uehara,Keisuke Izumi,Koji Tamada,Lieping Chen,Josef Penninger,Jun‐ichiro Inoue,Taishin Akiyama,Mitsuru Matsumoto
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2011-03-26
卷期号:186 (9): 5047-5057
被引量:83
标识
DOI:10.4049/jimmunol.1003533
摘要
Abstract It has recently become clear that signals mediated by members of the TNFR superfamily, including lymphotoxin-β receptor (LTβR), receptor activator for NF-κB (RANK), and CD40, play essential roles in organizing the integrity of medullary thymic epithelial cells (mTECs) required for the establishment of self-tolerance. However, details of the mechanism responsible for the unique and cooperative action of individual and multiple TNFR superfamily members during mTEC differentiation still remain enigmatic. In this study, we show that the LTβR signal upregulates expression of RANK in the thymic stroma, thereby promoting accessibility to the RANK ligand necessary for mTEC differentiation. Cooperation between the LTβR and RANK signals for optimal mTEC differentiation was underscored by the exaggerated defect of thymic organogenesis observed in mice doubly deficient for these signals. In contrast, we observed little cooperation between the LTβR and CD40 signals. Thus, the LTβR signal exhibits a novel and unique function in promoting RANK activity for mTEC organization, indicating a link between thymic organogenesis mediated by multiple cytokine signals and the control of autoimmunity.
科研通智能强力驱动
Strongly Powered by AbleSci AI