Identification of very early lymphoid precursors in bone marrow and their regulation by estrogen

被引:181
作者
Medina, KL [1 ]
Garrett, KP [1 ]
Thompson, LF [1 ]
Rossi, MID [1 ]
Payne, KJ [1 ]
Kincade, PW [1 ]
机构
[1] Oklahoma Med Res Fdn, Immunobiol & Canc Program, Oklahoma City, OK 73104 USA
关键词
D O I
10.1038/90659
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Estrogen is a negative regulator of lymphopoiesis and provides an experimental tool for probing relationships between lymphocyte precursors and stem cells. We found that expression of lymphocyte-associated genes and immunoglobulin (Ig) gene rearrangement occurred before CD45R acquisition. Lymphoid-restricted progenitors that were Lin-IL-7R alpha (+)c-kit(lo)TdT(+) (lineage marker-, interleukin receptor 7(alpha+), c-kit(lo) and terminal deoxynucleotidyl transferase(+)) were selectively depleted in estrogen-treated mice; within a less differentiated Lin-c-kit(hi) fraction, functional precursors of B and T, but not myeloid, cells were also selectively depleted. TdT and an Ig heavy chain transgene were detected within a hormone-regulated Lin-c-kit(hi)Sca-I(+)CD27(+)Flk-2(+)IL-7R alpha (-) subset of this multipotential progenitor population. Identification of these extremely early lymphoid precursors should facilitate investigation of the molecular mechanisms that control lineage-fate decisions in hematopoiesis.
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收藏
页码:718 / 724
页数:7
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