Notch1 expression in early lymphopoiesis influences B versus T lineage determination

被引:776
作者
Pui, JC
Allman, D
Xu, LW
DeRocco, S
Karnell, FG
Bakkour, S
Lee, JY
Kadesch, T
Hardy, RR
Aster, JC
Pear, WS [1 ]
机构
[1] Univ Penn, Med Ctr, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Med Ctr, Inst Med & Engn, Philadelphia, PA 19104 USA
[3] Univ Penn, Med Ctr, Dept Genet, Philadelphia, PA 19104 USA
[4] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[5] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1074-7613(00)80105-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Notch receptors regulate fate decisions in many cells. One outcome of Notch signaling is differentiation of bipotential precursors into one cell type versus another. To investigate consequences of Notch1 expression in hematolymphoid progenitors, mice were reconstituted with bone marrow (BM) transduced with retroviruses encoding a constitutively active form of Notch1. Although neither granulocyte or monocyte differentiation were appreciably affected, lymphopoiesis was dramatically altered. As early as 3 weeks following transplantation, mice receiving activated Notch1-transduced BM contained immature CD4(+)CD8(+) T cells in the BM and exhibited a simultaneous block in early B cell lymphopoiesis. These results suggest that Notch1 provides a key regulatory signal in determining T lymphoid versus B lymphoid lineage decisions, possibly by influencing lineage commitment from a common lymphoid progenitor cell.
引用
收藏
页码:299 / 308
页数:10
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