Development of V alpha 14(+) NK T cells in the early stages of embryogenesis

被引:48
作者
Makino, Y [1 ]
Kanno, R [1 ]
Koseki, H [1 ]
Taniguchi, M [1 ]
机构
[1] CHIBA UNIV,SCH MED,CTR BIOMED SCI,DIV MOLEC IMMUNOL,CHIBA 260,JAPAN
关键词
D O I
10.1073/pnas.93.13.6516
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
The majority of T lymphocytes start to develop at around day 15 of gestation (d15)-d17 in the thymus and comprise the peripheral repertoire characterized by the expression of polymorphic T-cell antigen receptors (TCRs). Contrary to these conventional T cells, a subset of T cells, called natural killer (NK) T cells (most of them expressing an invariant TCR encoded by the V alpha 14J alpha 281 gene with a 1-nt N-region), preferentially differentiates extrathymically and dominates the peripheral T-cell population at a high frequency (5% in splenic T cells and 40% in bone marrow T cells). sere, we investigated the development of NK T cells and found that the invariant V alpha 14(+) TCR transcripts and the circular DNA created by V alpha 14 and J alpha 281 gene rearrangements can be detected in the embryo body at d9.5 of gestation and in the yolk sac and the fetal liver at d11.5-d13.5 of gestation, but not in the thymus, whereas T cells with V alpha 1(+) TCR expression, a major population in the thymus, were not observed at these early stages of gestation, Fluorescence-activated cell sorter analysis also demonstrated that there exist CD3(+) alpha beta(+) T cells, almost all of which are V alpha 14/V beta 8(+) T cells, during early embryogenesis. To our knowledge, this demonstrates for the first time that a T lymphocyte subset develops in extrathymic tissues during the early stages of embryogenesis.
引用
收藏
页码:6516 / 6520
页数:5
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