Molecular and genetic parameters defining T-cell clonal selection

被引:22
作者
Labrecque, Nathalie [1 ,2 ,3 ]
Baldwin, Troy [4 ]
Lesage, Sylvie [1 ,3 ]
机构
[1] Maisonneuve Rosemont Hosp, Res Ctr, Montreal, PQ H1T 2M4, Canada
[2] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[3] Univ Montreal, Dept Microbiol & Immunol, Montreal, PQ H3C 3J7, Canada
[4] Univ Alberta, Dept Med Microbiol & Immunol, Edmonton, AB, Canada
关键词
negative selection; positive selection; thymus; THYMOCYTE POSITIVE SELECTION; SEVERE COMBINED IMMUNODEFICIENCY; STEROID-RECEPTOR NUR77; NEGATIVE SELECTION; THYMIC SELECTION; CENTRAL TOLERANCE; PROTEIN-KINASE; IN-VIVO; AUTOREACTIVE THYMOCYTES; CONFORMATIONAL-CHANGE;
D O I
10.1038/icb.2010.119
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Clonal selection of T cells occurs in the thymus and is responsible for generating a useful and functional repertoire of T cells. Aberrations in clonal selection result in altered T-cell homeostasis in the secondary lymphoid organs ranging from an absence of T cells to an overabundance of autoreactive T cells. The advent of new technologies facilitating the manipulation of the mouse genome has helped refine our understanding of the molecular and genetic pathways involved in clonal selection and has also revealed a high degree of complexity. Herein, we attempt to review recent advances in thymic selection processes, achieved mostly through genetic manipulations. Immunology and Cell Biology (2011) 89, 16-26; doi:10.1038/icb.2010.119; published online 19 October 2010
引用
收藏
页码:16 / 26
页数:11
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