Stat3 in thymic epithelial cells is essential for postnatal maintenance of thymic architecture and thymocyte survival

被引:84
作者
Sano, S
Takahama, Y
Sugawara, T
Kosaka, H
Itami, S
Yoshikawa, K
Miyazaki, J
van Ewijk, W
Takeda, J
机构
[1] Osaka Univ, Grad Sch Med, Dept Dermatol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Social Environm Med, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Med, Dept Physiol Chem & Nutr, Suita, Osaka 5650871, Japan
[4] Univ Tokushima, Inst Genome Res, Tokushima 7708503, Japan
[5] Erasmus Univ, Dept Immunol, NL-3000 DR Rotterdam, Netherlands
关键词
D O I
10.1016/S1074-7613(01)00180-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study describes abnormalities of the thymus in mice in which the Stat3 gene has been specifically disrupted behind the keratin 5 promoter. In these mice, virtually all of the thymic epithelial cells (TEC) were deficient for Stat3 activation. Adult mutant mice developed severe thymic hypoplasia, which included alterations in the cortical TEC architecture that coincided with the loss of thymocytes. Even during the asymptomatic period of preadolescence, these mice exhibited a higher susceptibility of the thymus to suboptimal doses of dexamethasone or gamma -irradiation, while their thymocytes per se were no more sensitive than controls. These results indicate that Stat3 in TEC plays an essential role in maintaining thymic architecture and thymocyte survival.
引用
收藏
页码:261 / 273
页数:13
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