Requirement for diverse, low-abundance peptides in positive selection of T cells

被引:94
作者
Barton, GM
Rudensky, AY
机构
[1] Univ Washington, Howard Hughes Med Inst, Sch Med, Seattle, WA 98195 USA
[2] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98195 USA
[3] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
关键词
D O I
10.1126/science.283.5398.67
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
Whether a single major histocompatibility complex (MHC)-bound peptide can drive the positive selection of large numbers of T cells has been-a controversial. issue. A diverse population of self peptides was shown to be essential for the in vivo development of CD4 T cells. Mice in which all but 5 percent of MHC class II molecules were bound by a single peptide had wild-type numbers of CD4 T cells. However, when the diversity within this 5 percent was lost, CD4 T cell development was impaired. Blocking the major peptide-MHC complex in thymus organ culture had no effect on T cell development; indicating that positive selection occurred on the diverse peptides present at low levels, This requirement for peptide diversity indicates that the interaction between self peptides and T cell receptors during positive selection is highly specific.
引用
收藏
页码:67 / 70
页数:4
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