Zoned out:: Functional mapping of stromal signaling microenvironments in the thymus

被引:344
作者
Petrie, Howard T. [1 ]
Zuniga-Pflucker, Juan Carlos
机构
[1] Scripps Florida Res Inst, Jupiter, FL 33458 USA
[2] Univ Toronto, Dept Immunol, Toronto, ON M4N 3M5, Canada
[3] Sunnybrook Res Inst, Toronto, ON M4N 3M5, Canada
关键词
thymus; T cell development; stromal cells; Notch ligands; IL-7; chemokines;
D O I
10.1146/annurev.immunol.23.021704.115715
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
All hematopoietic cells, including T lymphocytes, originate from stem cells that reside in the bone marrow. Most hernatopoietic lineages also mature in the bone marrow, but in this respect, T lymphocytes differ. Under normal circumstances, most T lymphocytes are produced in the thymus from marrow-derived progenitors that circulate in the blood. Cells that home to the thymus from the marrow possess the potential to generate multiple T and non-T lineages. However, there is little evidence to suggest that, once inside the thymus, they give rise to anything other than T cells. Thus, signals unique to the thymic microenvironment compel multipotent progenitors to commit to the T lineage, at the expense of other potential lineages. Summarizing what is known about the signals the thymus delivers to uncommitted progenitors, or to immature T-committed progenitors, to produce functional T cells is the focus of this reviews
引用
收藏
页码:649 / 679
页数:31
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