Runx1 is essential for hematopoietic commitment at the hemangioblast stage of development in vitro

被引:228
作者
Lacaud, G
Gore, L
Kennedy, M
Kouskoff, V
Kingsley, P
Hogan, C
Carlsson, L
Speck, N
Palis, J
Keller, G [1 ]
机构
[1] Mt Sinai Sch Med, Carl C Icahn Inst Gene Therapy & Mol Med, New York, NY 10029 USA
[2] Univ Colorado, Dept Pediat, Div Hematol Oncol, Ctr Hlth Sci, Boulder, CO 80309 USA
[3] Univ Colorado, Div Med Oncol, Ctr Hlth Sci, Boulder, CO 80309 USA
[4] Childrens Hosp, Denver, CO 80218 USA
[5] Univ Rochester, Dept Pediat, Rochester, NY USA
[6] Univ Rochester, Ctr Human Genet & Mol Pediat Dis, Rochester, NY USA
[7] Umea Univ, Dept Mol Biol, Umea, Sweden
[8] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Biochem, Hanover, NH 03756 USA
关键词
D O I
10.1182/blood-2001-12-0321
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this report we demonstrate a role for Runx1 (AML1)at the hemangloblast stage of hematopoietic and endothelial development in embryonic stem (ES) cell-derived embryoid bodies (EBs). Runx1 is expressed in EBs during the appearance of precursors with hemangloblast properties, the blast colony-forming cells (BL-CFCs). Cell sorting studies revealed that all BL-CFCs within EBs express Runx1. Runx1-deficient EBs consistently generate 10- to 20-fold fewer blast colonies than wild-type controls and display a complete block in definitive hematopoiesis. Despite this defect, Runx1(-/-) EBs and yolk sacs from mutant embryos generate normal numbers of primitive erythroid precursors. These observations clearly demonstrate that Runx1 functions early in hematopoietic development, and they support the interpretation that the primitive erythroid lineage Is established early by a subset of BL-CFCs that develop In a Runx1-independent fashion. (Blood. 2002; 100:458-466) (C) 2002 by The American Society of Hematology.
引用
收藏
页码:458 / 466
页数:9
相关论文
共 57 条
[2]   THE GENE SCL IS EXPRESSED DURING EARLY HEMATOPOIESIS AND ENCODES A DIFFERENTIATION-RELATED DNA-BINDING MOTIF [J].
BEGLEY, CG ;
APLAN, PD ;
DENNING, SM ;
HAYNES, BF ;
WALDMANN, TA ;
KIRSCH, IR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :10128-10132
[3]  
BRADY G, 1990, Methods in Molecular and Cellular Biology, V2, P17
[4]   HEMOGLOBIN ONTOGENY DURING NORMAL MOUSE FETAL DEVELOPMENT [J].
BROTHERTON, TW ;
CHUI, DHK ;
GAULDIE, J ;
PATTERSON, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (06) :2853-2857
[5]  
BURKERT U, 1991, NEW BIOL, V3, P698
[6]  
Choi K, 1998, DEVELOPMENT, V125, P725
[7]  
DIETERLENLIEVRE F, 1975, J EMBRYOL EXP MORPH, V33, P607
[8]   DIFFUSE INTRAEMBRYONIC HEMATOPOIESIS IN NORMAL AND CHIMERIC AVIAN DEVELOPMENT [J].
DIETERLENLIEVRE, F ;
MARTIN, C .
DEVELOPMENTAL BIOLOGY, 1981, 88 (01) :180-191
[9]  
DOETSCHMAN TC, 1985, J EMBRYOL EXP MORPH, V87, P27
[10]  
DUMONT DJ, 1992, ONCOGENE, V7, P1471