Stromal expression of Jagged 1 promotes colony formation by fetal hematopoietic progenitor cells

被引:135
作者
Jones, P
May, G
Healy, L
Brown, J
Hoyne, G
Delassus, S
Enver, T
机构
[1] Inst Canc Res, Chester Beatty Labs, Sect Gene Funct & Regulat, London SW3 6JB, England
[2] Inst Canc Res, Chester Beatty Labs, Leukaemia Res Fund Ctr, London SW3 6JB, England
[3] Univ Edinburgh, Dept Resp Med, Edinburgh, Midlothian, Scotland
关键词
D O I
10.1182/blood.V92.5.1505.417k42_1505_1511
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Notch signaling system regulates proliferation and differentiation in many tissues. Notch is a transmembrane receptor activated by ligands expressed on adjacent cells. Hematopoietic stem cells and early progenitors express Notch, making the stromal cells which form cell-cell contacts with progenitor cells candidate ligand-presenting cells in the hematopoietic microenvironment. Therefore, we examined primary stromal eel cultures for expression of Notch ligands. Using reverse transcription-polymerase chain reaction, in situ hybridization, immunohistochemistry, and Western blotting, we demonstrate expression of Jagged 1 in primary stromal cultures. To investigate if the stromal expression of Jagged 1 has functional effects on hematopoietic progenitors, we cultured CD34(+), c-kit(+) hematopoietic progenitor cells derived from the aorto gonadal mesonephros region of day 11 mouse embryos on the Jagged 1(-) stromal cell line S17 and on S17 cells engineered to express Jagged 1. The presence of Jagged 1 increased the number of colonies formed in subsequent methylcellulose culture fourfold. Larger increases in colony numbers were observed under the same culture conditions with CD34(+), c-kit(+) hematopoietic progenitor cells derived from d11 fetal liver. These results obtained in vitro table Jagged 1 as a candidate regulator of stem cell fate in the context of stromal microenvironments in vivo. (C) 1998 by The American Society of Hematology.
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收藏
页码:1505 / 1511
页数:7
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