The deubiquitinating enzyme CYLD regulates the differentiation and maturation of thymic medullary epithelial cells

被引:17
|
作者
Reissig, Sonja [1 ]
Hoevelmeyer, Nadine [1 ]
Tang, Yilang [1 ]
Weih, Debra [2 ]
Nikolaev, Alexey [1 ]
Riemann, Marc [2 ]
Weih, Falk [2 ]
Waisman, Ari [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Mol Med, D-55131 Mainz, Germany
[2] Leibniz Inst Age Res Fritz Lipmann Inst FLI, Immunol Grp, Jena, Germany
来源
IMMUNOLOGY AND CELL BIOLOGY | 2015年 / 93卷 / 06期
关键词
NF-KAPPA-B; T-CELLS; SELF-TOLERANCE; TRANSGENIC MICE; DEFICIENT MICE; THYMOCYTES; EXPRESSION; MICROENVIRONMENT; SELECTION; FAMILY;
D O I
10.1038/icb.2014.122
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cross talk between thymocytes and the thymic epithelium is critical for T-cell development and the establishment of central tolerance. Medullary thymic epithelial cells (mTECs) are located in the thymic medulla and mediate the elimination of self-reactive thymocytes, thereby preventing the onset of autoimmunity. Previous studies identified the deubiquitinating enzyme CYLD as a critical regulator of T-cell development by activating proximal T-cell receptor signaling during the transition of double-positive to single-positive thymocytes. Here we evaluated the impact of the naturally occurring short-splice variant of the cyld gene (sCYLD) on the development and maturation of mTECs. We found that thymi of CYLDex7/8 mice, solely expressing sCYLD, displayed a reduced number of mature mTECs caused by a developmental block during the transition of immature to mature mTECs. Further, we could demonstrate an impaired negative selection of thymocytes in these mice. Our data demonstrate that inefficient negative selection in the thymus of CYLDex7/8 mice result from a defect in mTEC maturation.
引用
收藏
页码:558 / 566
页数:9
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