Identification of a novel developmental stage marking lineage commitment of progenitor thymocytes

被引:116
作者
Carlyle, JR
Michie, AM
Furlonger, C
Nakano, T
Lenardo, MJ
Paige, CJ
ZunigaPflucker, JC
机构
[1] UNIV TORONTO,DEPT IMMUNOL,TORONTO,ON M5S 1A8,CANADA
[2] UNIV TORONTO,WELLESLEY HOSP,RES INST,TORONTO,ON M4Y 1J3,CANADA
[3] OSAKA UNIV,MICROBIAL DIS RES INST,DEPT MOL CELL BIOL,SUITA,OSAKA 565,JAPAN
[4] NIAID,IMMUNOL LAB,NIH,BETHESDA,MD 20892
关键词
D O I
10.1084/jem.186.2.173
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bipotent progenitors for T and natural killer (NK) lymphocytes are thought to exist among early precursor thymocytes. The identification and functional properties of such a progenitor population remain undefined. We report the identification of a novel developmental stage during fetal thymic ontogeny that delineates a population of T/NK-committed progenitors (NK1.1(+)/CD117(+)/CD44(+)/CD25(-)). Thymocytes at this stage in development are phenotypically and functionally distinguishable from the pool of multipotent lymphoid-restricted (B, T, and NK) precursor thymocytes. Exposure of multipotent precursor thymocytes or fetal liver-derived hematopoietic progenitors to thymic stroma induces differentiation to the bipotent developmental stage. Continued exposure to a thymic microenvironment results in predominant commitment to the T cell lineage, whereas coculture with a bone marrow-derived stromal cell line results in the generation of mature NK cells. Thus, the restriction point to T and NK lymphocyte destinies from a multipotent progenitor stage is marked by a thymus-induced differentiation step.
引用
收藏
页码:173 / 182
页数:10
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