Maintenance of TCR clonality in T cells expressing genes for two TCR heterodimers

被引:31
作者
Sant'Angelo, DB [1 ]
Cresswell, P
Janeway, CA
Denzin, LK
机构
[1] Cornell Univ, Weill Grad Sch Med Sci, Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10021 USA
[2] Yale Univ, Howard Hughes Med Inst, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
关键词
D O I
10.1073/pnas.121179998
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
T cell receptor (TCR) allelic exclusion is believed to be primarily mediated by suppression of further recombination at the TCR locus after the expression of a functional TCR protein. Genetic allelic exclusion has been shown to be leaky for the P chain and, more commonly, for the rr chain. Here, we demonstrate an additional mechanism by which T cells can maintain monoclonality. T cells from double TCR transgenic mice express only one or the other of the two available TCRs at the cell surface. This "functional allelic exclusion" is apparently due to control of the TCR assembly process because these T cells express RNA and protein for all four transgenic TCR proteins. Lack of cell surface expression of the second TCR may be controlled by a failure to assemble the TCR heterodimer.
引用
收藏
页码:6824 / 6829
页数:6
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