Stepwise development of committed progenitors in the bone marrow that generate functional T cells in the absence of the thymus

被引:26
作者
García-Ojeda, ME
Dejbakhsh-Jones, S
Chatterjea-Matthes, D
Mukhopadhyay, A
BitMansour, A
Weissman, IL
Brown, JMY
Strober, S
机构
[1] Stanford Univ, Sch Med, Ctr Clin Sci, Dept Med,Div Immunol & Rheumatol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
关键词
D O I
10.4049/jimmunol.175.7.4363
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We identified committed T cell progenitors (CTPs) in the mouse bone marrow that have not rearranged the TCR beta gene; express a variety of genes associated with commitment to the T cell lineage, including GATA-3, T cell-specific factor-1, C beta, and Id2; and show a surface marker pattern (CD44(+)CD25(-)CD24(+)CD5(-)) that is similar to the earliest T cell progenitors in the thymus. More mature committed intermediate progenitors in the marrow have rearranged the TCR gene loci, express V alpha and V beta genes as well as CD3 epsilon, but do not express surface TCR or CD3 receptors. CTPs, but not progenitors from the thymus, reconstituted the alpha beta T cells in the lymphoid tissues of athymic nu/nu mice. These reconstituted T cells vigorously secreted IFN-gamma after stimulation in vitro, and protected the mice against lethal infection with murine CMV. In conclusion, CTPs in wild-type bone marrow can generate functional T cells via an extrathymic pathway in athymic nu/nu mice.
引用
收藏
页码:4363 / 4373
页数:11
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