Interleukin 7 receptor-deficient mice lack gamma delta T cells

被引:278
作者
Maki, K
Sunaga, S
Komagata, Y
Kodaira, Y
Mabuchi, A
Karasuyama, H
Yokomuro, K
Miyazaki, J
Ikuta, K
机构
[1] UNIV TOKYO,FAC MED,DEPT DIS RELATED GENE REGULAT RES SANDOZ,BUNKYO KU,TOKYO 113,JAPAN
[2] NIPPON MED COLL,DEPT MICROBIOL & IMMUNOL,TOKYO 113,JAPAN
[3] NIPPON MED COLL,DEPT SURG 2,TOKYO 113,JAPAN
[4] TOKYO METROPOLITAN INST MED SCI,DEPT IMMUNOL,TOKYO 113,JAPAN
[5] TOHOKU UNIV,INST DEV AGING & CANC,SENDAI,MIYAGI 98077,JAPAN
关键词
homologous recombination; T-cell differentiation; cytokine; thymus; intraepithelial lymphocyte;
D O I
10.1073/pnas.93.14.7172
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The interleukin 7 receptor (IL-7R) plays a crucial role in early B- and T-cell development. It consists of a unique alpha chain and a common gamma chain [IL-2 receptor gamma chain (IL-2R gamma)]. Gene inactivation of IL-7, IL-7R, and IL-2R gamma resulted in severe impairment of B and T lymphopoiesis in mice. In addition, IL-2R gamma-deficient mice lack gamma delta T cells in the skin and have the impaired development of natural killer (NK) cells and intraepithelial lymphocytes. To explore the role of IL-7/IL-7R system in gamma delta T- and NK-cell development, we have generated and analyzed IL-7R-deficient mice. gamma delta T cells were absent from skin, gut, liver, and spleen in the deficient mice. In contrast, alpha beta T and B cells were detected in reduced, but certain, numbers, and NK cells developed normally, The gamma delta T-cell development in fetal and adult thymus was also completely blocked. These results clearly demonstrate that the signal from IL-7R is indispensable for gamma delta T-cell development in both thymic and extrathymic pathways. On the contrary, it is suggested that NK-cell development requires cytokine(s) other than IL-7.
引用
收藏
页码:7172 / 7177
页数:6
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