Wnt, activin, and BMP signaling regulate distinct stages in the developmental pathway from embryonic stem cells to blood

被引:241
作者
Nostro, M. Cristina [1 ]
Cheng, Xin [2 ]
Keller, Gordon M. [1 ,2 ]
Gadue, Paul [2 ]
机构
[1] Univ Hlth Network, McEwen Ctr Regenerat Med, Toronto, ON M5G 1L7, Canada
[2] Mt Sinai Sch Med, Dept Gen & Cell Med, New York, NY 10029 USA
关键词
D O I
10.1016/j.stem.2007.10.011
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The embryonic stem cell differentiation system was used to define the roles of the Activin/Nodal, BMP, and canonical Wnt signaling pathways at three distinct developmental stages during hematopoietic ontogeny: induction of a primitive streak-like population, formation of Flk1(+) mesoderm, and induction of hematopoietic progenitors. Activin/Nodal and Wnt, but not BMP, signaling are required for the induction of the primitive streak. Although BMP is not required for primitive streak induction, it displays a strong posteriorizing effect on this population. All three signaling pathways regulate induction of Flk1(+) mesoderm. The specification of Flk1(+) mesoderm to the hematopoietic lineages requires VEGF and Wnt, but not BMP or Activin/Nodal signaling. Specifically, Wnt signaling is essential for commitment of the primitive erythroid, but not the definitive lineages. These findings highlight dynamic changes in signaling requirements during blood cell development and identify a role for Wnt signaling in the establishment of the primitive erythroid lineage.
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收藏
页码:60 / 71
页数:12
相关论文
共 49 条
[1]   MOLECULAR AND CELLULAR PROPERTIES OF PECAM-1 (ENDOCAM/CD31) - A NOVEL VASCULAR CELL CELL-ADHESION MOLECULE [J].
ALBELDA, SM ;
MULLER, WA ;
BUCK, CA ;
NEWMAN, PJ .
JOURNAL OF CELL BIOLOGY, 1991, 114 (05) :1059-1068
[2]   The organizer factors Chordin and Noggin are required for mouse forebrain development [J].
Bachiller, D ;
Klingensmith, J ;
Kemp, C ;
Belo, JA ;
Anderson, RM ;
May, SR ;
McMahon, JA ;
McMahon, AP ;
Harland, RM ;
Rossant, J ;
De Robertis, EM .
NATURE, 2000, 403 (6770) :658-661
[3]   The specification of early hernatopoiesis in the mammal [J].
Baron, Margaret H. ;
Fraser, Stuart T. .
CURRENT OPINION IN HEMATOLOGY, 2005, 12 (03) :217-221
[4]   Axis development and early asymmetry in mammals [J].
Beddington, RSP ;
Robertson, EJ .
CELL, 1999, 96 (02) :195-209
[5]   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
[6]   BMP type II receptor is required for gastrulation and early development of mouse embryos [J].
Beppu, H ;
Kawabata, M ;
Hamamoto, T ;
Chytil, A ;
Minowa, O ;
Noda, T ;
Miyazono, K .
DEVELOPMENTAL BIOLOGY, 2000, 221 (01) :249-258
[7]  
CANDIA AF, 1992, DEVELOPMENT, V116, P1123
[8]  
Choi K, 1998, DEVELOPMENT, V125, P725
[9]  
CONLON FL, 1994, DEVELOPMENT, V120, P1919
[10]   Smad-dependent and Smad-independent pathways in TGF-β family signalling [J].
Derynck, R ;
Zhang, YE .
NATURE, 2003, 425 (6958) :577-584