Hedgehog signaling is required for adult blood stem cell formation in zebrafish embryos

被引:283
作者
Gering, M [1 ]
Patient, R [1 ]
机构
[1] Univ Nottingham, Inst Genet, Queens Med Ctr, Nottingham NG7 2UH, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.devcel.2005.01.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Studies with embryonic explants and embryonic stem cells have suggested a role for Hedgehog (Hh) signaling in hematopoiesis. However, targeted deletion of Hh pathway components in the mouse has so far failed to provide in vivo evidence. Here we show that zebrafish embryos mutant in the Hh pathway or treated with the Hh signaling inhibitor cyclopamine display defects in adult hematopoietic stem cell (HSC) formation but not in primitive hematopoiesis. Hh is required in the trunk at three consecutive stages during vascular development: for the medial migration of endothelial progenitors of the dorsal aorta (DA), for arterial gene expression, and for the formation of intersomitic vessel sprouts. Interference with Hh signaling during the first two stages also interferes with HSC formation. Furthermore, HSC and DA formation also share Vegf and Notch requirements, which further distinguishes them from primitive hernatopoiesis and underlines their close relationship during vertebrate development.
引用
收藏
页码:389 / 400
页数:12
相关论文
共 81 条
[21]   DIFFUSE INTRAEMBRYONIC HEMATOPOIESIS IN NORMAL AND CHIMERIC AVIAN DEVELOPMENT [J].
DIETERLENLIEVRE, F ;
MARTIN, C .
DEVELOPMENTAL BIOLOGY, 1981, 88 (01) :180-191
[22]   Dosage-sensitive requirement for mouse D114 in artery development [J].
Duarte, A ;
Hirashima, M ;
Benedito, R ;
Trindade, A ;
Diniz, P ;
Bekman, E ;
Costa, L ;
Henrique, D ;
Rossant, J .
GENES & DEVELOPMENT, 2004, 18 (20) :2474-2478
[23]  
Dyer MA, 2001, DEVELOPMENT, V128, P1717
[24]   PATTERNING ACTIVITIES OF VERTEBRATE HEDGEHOG PROTEINS IN THE DEVELOPING EYE AND BRAIN [J].
EKKER, SC ;
UNGAR, AR ;
GREENSTEIN, P ;
VONKESSLER, DP ;
PORTER, JA ;
MOON, RT ;
BEACHY, PA .
CURRENT BIOLOGY, 1995, 5 (08) :944-955
[25]   Combinatorial effects of Flk1 and Tal1 on vascular and hematopoietic development in the mouse [J].
Ema, M ;
Faloon, P ;
Zhang, WL ;
Hirashima, M ;
Reid, T ;
Stanford, WL ;
Orkin, S ;
Choi, K ;
Rossant, J .
GENES & DEVELOPMENT, 2003, 17 (03) :380-393
[26]   Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene [J].
Ferrara, N ;
CarverMoore, K ;
Chen, H ;
Dowd, M ;
Lu, L ;
OShea, KS ;
PowellBraxton, L ;
Hillan, KJ ;
Moore, MW .
NATURE, 1996, 380 (6573) :439-442
[27]   The Notch target genes Hey1 and Hey2 are required for embryonic vascular development [J].
Fischer, A ;
Schumacher, N ;
Maier, M ;
Sendtner, M ;
Gessler, M .
GENES & DEVELOPMENT, 2004, 18 (08) :901-911
[28]   Vessel patterning in the embryo of the zebrafish: Guidance by notochord [J].
Fouquet, B ;
Weinstein, BM ;
Serluca, FC ;
Fishman, MC .
DEVELOPMENTAL BIOLOGY, 1997, 183 (01) :37-48
[29]  
GARCIAPORRERO JA, 1995, ANAT EMBRYOL, V192, P427
[30]   A γ-secretase inhibitor blocks Notch signaling in vivo and causes a severe neurogenic phenotype in zebrafish [J].
Geling, A ;
Steiner, H ;
Willem, M ;
Bally-Cuif, L ;
Haass, C .
EMBO REPORTS, 2002, 3 (07) :688-694