The Scurfy mutation of FoxP3 in the thymus stroma leads to defective thymopoiesis

被引:74
作者
Chang, X
Gao, JX [1 ]
Jiang, Q
Wen, J
Seifers, N
Su, LS
Godfrey, VL
Zuo, T
Zheng, P
Liu, Y
机构
[1] Ohio State Univ, Med Ctr, Dept Pathol, Div Canc Immunol, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[3] Univ N Carolina, Dept Immunol & Microbiol, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
关键词
D O I
10.1084/jem.20050157
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Scurfy mutation of the FoxP3 gene (FoxP3(sf)) in the mouse and analogous mutations in human result in lethal autoimmunity. The mutation of FoxP3 in the hematopoietic cells impairs the development of regulatory T cells. In addition, development of the Scurfy disease also may require mutation of the gene in nonhematopoietic cells. The T cell-extrinsic function of FoxP3 has not been characterized. Here we show that the FoxP3(sf) mutation leads to defective thymopoiesis, which is caused by inactivation of FoxP3 in the thymic stromal cells. FoxP3 mutation also results in overexpression of ErbB2 in the thymic stroma, which may be involved in defective thymopoiesis. Our data reveal a novel T cell-extrinsic function of FoxP3. In combination, the T cell-intrinsic and -extrinsic defects provide plausible explanation for the severity of the autoimmune diseases in the scurfy mice and in patients who have immunodysregulation, polyendocrinopathy, enteropathy, and X-linked syndrome.
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页码:1141 / 1151
页数:11
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