THE LEVEL OF N-REGION DIVERSITY IN T-CELL RECEPTORS IS NOT PRE-ORDAINED IN THE STEM-CELL

被引:26
作者
BOGUE, M
MOSSMANN, H
STAUFFER, U
BENOIST, C
MATHIS, D
机构
[1] FAC MED STRASBOURG,INST CHIM BIOL,CNRS,GENET MOLEC EUCARYOTES LAB,INSERM,F-67085 STRASBOURG,FRANCE
[2] MAX PLANCK INST IMMUNOBIOL,FREIBURG,GERMANY
关键词
DIVERSITY; T-CELL RECEPTOR; TERMINAL DEOXYNUCLEOTIDYL TRANSFERASE; NEONATE; SCID MICE;
D O I
10.1002/eji.1830230533
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The alphabeta Tcell repertoires of adults and neonates are distinctly different. For example, T cell receptors (TcR) from adult animals have substantial N-nucleotide addition at their V-D-J junctions while those from neonatal animals do not. This dichotomy reflects a rather abrupt change in expression of the terminal deoxynucleotidyl transferase (TdT) gene in thymocytes on day 4 after birth. We have asked whether this change is due to the differentiation of successive waves of stem cells harboring different potentials for TdT expression, a scenario like the one proposed to explain developmental regulation of gammadelta T cell repertoires. Reconstitution of adult severe combined immunodeficiency mice with either fetal liver or adult bone marrow precursors gave rise to T cells with substantial N-region diversity in their TcR, even at the earliest points of reconstitution. It is most likely, then, that the abrupt change in TdT gene expression in day 4 thymocytes is due to an environmentally induced switch-on.
引用
收藏
页码:1185 / 1188
页数:4
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