Hematopoietic cell development in the zebrafish embryo

被引:63
作者
Bertrand, Julien Y. [1 ]
Traver, David [1 ,2 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
developmental hematopoiesis; hemangioblast; hematopoietic stem cells; hemogenic endothelium; zebrafish; STEM-CELLS; DEFINITIVE HEMATOPOIESIS; TRANSGENIC ZEBRAFISH; YOLK-SAC; ENDOTHELIAL LINEAGES; VASCULAR DEVELOPMENT; EXPRESSION; BLOOD; MOUSE; PRECURSORS;
D O I
10.1097/MOH.0b013e32832c05e4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review A wealth of new experimental evidence has been published over the past year that has helped refine our models of blood cell development. We will review this information, discuss the current models of hematopoietic ontogeny and provide perspective on current and future research directions, with an emphasis on how studies in the zebrafish are helping us better understand how hematopoietic stem cells are formed in the vertebrate embryo. Recent findings Several important studies have been published recently addressing the embryonic development of hematopoietic stem cells. These studies have helped clarify several controversial topics in developmental hematopoiesis, including the concepts of the hemangioblast and hemogenic endothelium. In particular, the postulate that hematopoietic stem cells arise through hemogenic endothelial intermediates has been greatly strengthened by a collection of convincing publications reviewed below. Summary A precise understanding of how hematopoietic stem cells are patterned during development has important implications for both developmental biology and regenerative medicine. Since hematopoietic stem cells are the only hematopoietic cells capable of lifelong, multilineage blood cell production, understanding the stepwise, molecular processes of their instruction from mesoderm is key to replicating these events in vitro from pluripotent embryonic stem cells.
引用
收藏
页码:243 / 248
页数:6
相关论文
共 58 条
[1]   Genetic and cellular analyses of zebrafish atrioventricular cushion and valve development [J].
Beis, D ;
Bartman, T ;
Jin, SW ;
Scott, IC ;
D'Amico, LA ;
Ober, EA ;
Verkade, H ;
Frantsve, J ;
Field, HA ;
Wehman, A ;
Baier, H ;
Tallafuss, A ;
Bally-Cuif, L ;
Chen, JN ;
Stainier, DYR ;
Jungblut, B .
DEVELOPMENT, 2005, 132 (18) :4193-4204
[2]   CD41+ cmyb+ precursors colonize the zebrafish pronephros by a novel migration route to initiate adult hematopoiesis [J].
Bertrand, Julien Y. ;
Kim, Albert D. ;
Teng, Shutian ;
Traver, David .
DEVELOPMENT, 2008, 135 (10) :1853-1862
[3]   Definitive hematopoiesis initiates through a committed erythromyeloid progenitor in the zebrafish embryo [J].
Bertrand, Julien Y. ;
Kim, Albert D. ;
Violette, Emily P. ;
Stachura, David L. ;
Cisson, Jennifer L. ;
Traver, David .
DEVELOPMENT, 2007, 134 (23) :4147-4156
[4]   Three pathways to mature macrophages in the early mouse yolk sac [J].
Bertrand, JY ;
Jalil, A ;
Klaine, M ;
Jung, S ;
Cumano, A ;
Godin, I .
BLOOD, 2005, 106 (09) :3004-3011
[5]   Characterization of purified intraembryonic hematopoietic stem cells as a tool to define their site of origin [J].
Bertrand, JY ;
Giroux, S ;
Golub, R ;
Klaine, M ;
Jalil, A ;
Boucontet, L ;
Godin, I ;
Cumano, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (01) :134-139
[6]   Hematopoietic stem cell fate is established by the Notch-Runx pathway [J].
Burns, CE ;
Traver, D ;
Mayhall, E ;
Shepard, JL ;
Zon, LI .
GENES & DEVELOPMENT, 2005, 19 (19) :2331-2342
[7]   Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter [J].
Chen, Michael J. ;
Yokomizo, Tomomasa ;
Zeigler, Brandon M. ;
Dzierzak, Elaine ;
Speck, Nancy A. .
NATURE, 2009, 457 (7231) :887-891
[8]  
Choi K, 1998, DEVELOPMENT, V125, P725
[9]   Lymphoid potential, probed before circulation in mouse, is restricted to caudal intraembryonic splanchnopleura [J].
Cumano, A ;
DieterlenLievre, F ;
Godin, I .
CELL, 1996, 86 (06) :907-916
[10]   Intraembryonic, but not yolk sac hematopoietic precursors, isolated before circulation, provide long-term multilineage reconstitution [J].
Cumano, A ;
Ferraz, JC ;
Klaine, M ;
Di Santo, JP ;
Godin, I .
IMMUNITY, 2001, 15 (03) :477-485