Lymphotoxin Signal Promotes Thymic Organogenesis by Eliciting RANK Expression in the Embryonic Thymic Stroma
Author(s) -
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,
Junichiro Inoue,
Taishin Akiyama,
Mitsuru Matsumoto
Publication year - 2011
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1003533
Subject(s) - lymphotoxin , biology , organogenesis , microbiology and biotechnology , autoimmune regulator , stroma , receptor , embryonic stem cell , immunology , cytokine , autoimmunity , immune system , genetics , gene , immunohistochemistry
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.
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