ANALYSIS OF EARLY FETAL T-CELL RECEPTOR SIGMA-CHAIN IN HUMANS

被引:16
作者
VANDERSTOEP, N
DEKRIJGER, R
BRUINING, J
KONING, F
VANDENELSEN, P
机构
[1] UNIV HOSP LEIDEN, DEPT IMMUNOHAEMATOL, BLDG 1, E3-Q, POB 9600, 2300 RC LEIDEN, NETHERLANDS
[2] UNIV HOSP LEIDEN, BLOODBANK, 2300 RC LEIDEN, NETHERLANDS
[3] ERASMUS UNIV, DEPT PEDIAT, SUBDIV CLIN GENET, 3000 DR ROTTERDAM, NETHERLANDS
[4] ERASMUS UNIV, SOPHIA CHILDRENS HOSP, 3000 DR ROTTERDAM, NETHERLANDS
关键词
D O I
10.1007/BF00211647
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In the mouse it has been found that a number of T-cell receptor (Tcr) gd phenotypes are generated during fetal thymic development. To examine whether such "waves" of Tcrgd phenotypes can be found in man, we studied the V-region usage and junctional diversity of the T-cell receptor δ chain in human fetal and post-partum thymocytes and peripheral blood T cells. Using the polymerase chain reaction (PCR)-amplification technique it was found that in fetal thymocytes of 15-17 weeks of gestation the Tcrd-V3 gene segment was mainly employed, whereas in post-partum thymocytes the Tcrd-V1 gene segment was preferentially used. These Tcrd-V3 transcripts contained only a single D element (Dδ3) and a limited random nucleotide insertion. The Dδ3 element was also present in Tcrd-V3-containing transcripts derived from peripheral blood γδ Tcr+ clones. These data suggest that a wave of Tcr γδ might exist early in human fetal development that preferentially use the Tcrd-V3 gene segment. © 1990 Springer-Verlag.
引用
收藏
页码:331 / 336
页数:6
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