TGF-β type II receptor expression in thymic epithelial cells inhibits the development of Hassalls corpuscles in mice

被引:21
作者
Odaka, Chikako [1 ]
Hauri-Hohl, Mathias [2 ,3 ]
Takizawa, Kazuya [1 ]
Nishikawa, Yomiko [5 ]
Yano, Masashi [5 ]
Matsumoto, Mitsuru [5 ]
Boyd, Richard [6 ]
Hollaender, Georg A. [2 ,3 ,4 ]
机构
[1] Natl Inst Infect Dis, Dept Safety Res Blood & Biol Prod, Tokyo 2080011, Japan
[2] Univ Basel, Dept Biomed, Lab Pediat Immunol, CH-4058 Basel, Switzerland
[3] Univ Childrens Hosp, CH-4058 Basel, Switzerland
[4] Univ Oxford, Dept Paediat, Oxford, England
[5] Univ Tokushima, Inst Enzyme Res, Div Mol Immunol, Tokushima 7708503, Japan
[6] Monash Univ, Monash Immunol & Stem Cell Labs, Clayton, Vic 3800, Australia
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
epithelial cells; Hassalls corpuscle; MTS24; TGF- type II receptor; thymus; SEVERE COMBINED IMMUNODEFICIENCY; REGULATORY T-CELLS; MEDULLARY EPITHELIUM; HUMAN THYMOCYTES; GUINEA-PIG; MICROENVIRONMENT; DIFFERENTIATION; PROGENITOR; HETEROGENEITY; LOCALIZATION;
D O I
10.1093/intimm/dxt026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TGF-RII signaling prevents the development of Hassalls corpuscles.Hassalls corpuscles are concentric clusters of keratinized epithelial cells located within the thymic medulla of humans and guinea pigs but are scant in mouse and rat. They are considered to be the terminally differentiated stages of medullary thymic epithelial cells (mTECs) but the mechanisms of their origin are unclear. We have previously deleted the TGF- type II receptor (TGFRII) specifically in mouse TECs and reported that these mice have mitigated thymic involution and exhibit earlier reconstitution post-irradiation. In this study, we analyzed the differentiation of mTECs in the TGFRII-knockout mice. Interestingly, the TGFRII-knockout mice display enhanced development of Hassalls corpuscles. The expression of Aire, stromal-cell-derived factor 1 and thymic stromal lymphopoietin in the thymi of the TGFRII-knockout mice was similar to that previously reported for the human thymus. In addition, the putative epithelial progenitor markers MTS20 and MTS24 labeled Hassalls corpuscles in normal mice, but the extent and intensity of this staining were greatly enhanced in Hassalls corpuscles of the TGFRII-knockout mice. The phosphorylated forms of ERK and JNK were also found in Hassalls corpuscles of the TGFRII-knockout mice. Taken together, we suggest that TGFRII-mediated signaling in TECs inhibits their development into Hassalls corpuscles in mice.
引用
收藏
页码:633 / 642
页数:10
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