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T cell receptor germline gene segments and HLA haplotypes control the length of the CDR3 of human T cell receptor beta chains
被引:8
作者:
Kayser, C
Waase, I
Weyand, CM
Goronzy, JJ
机构:
[1] Department of Medicine, Division of Rheumatology, Mayo Clinic and Foundation, Rochester
关键词:
D O I:
10.1006/cimm.1996.0071
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The third complementarity determining region (CDR3) is the most variable part of alpha beta T cell receptors (TCR) and represents the putative antigen contacting site, To identify parameters determining the structural diversity of the CDR3 region, the CDR3 length distributions of 66 BV-J combinations in peripheral CD4(+) T cells (6 BV and fl BJ gene segments) of 12 unrelated individuals were analyzed. The median CDR3 length ranged from 8 to 12.5 amino acids and was partially determined by the usage of the BV and BJ gene segment. Beyond the influence of germline-encoded TCR gene segments, donors expressed an individual pattern of preferred CDR3 size classes, To identify mechanisms determining this individual pattern, 17 first-degree relatives from five families were studied, CDR3 length profiles were shared by some but not all relatives, Sharing of CDR3 length profiles correlated with the inheritance of both HLA-DR haplotypes. These data suggest that the length of the TCR beta chain is selected and that restrictions on the diversity of the CDR3 length are imposed by germline-encoded TCR gene segments as well as by major histocompatibility complex-dependent mechanisms. (C) 1996 Academic Press, Inc.
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页码:235 / 242
页数:8
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