Negative regulation of primitive hematopoiesis by the FGF signaling pathway

Blood

Volumn 108, Issue 10, 2006, Pages 3335-3343

  Nakazawa, Fumie ^a   Nagai, Hiroki ^a   Shin, Masahiro ^a   Sheng, Guojun ^a  

^a RIKEN Center for Biosystems Dynamics Research   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR; FIBROBLAST GROWTH FACTOR RECEPTOR 2; HEMOGLOBIN; MESSENGER RNA; TRANSCRIPTION FACTOR GATA 1; VASCULOTROPIN RECEPTOR 2;

ANIMAL TISSUE; ARTICLE; BLOOD CELL; CELL DIFFERENTIATION; CELL MIGRATION; CHICK; EMBRYO; HEMATOPOIESIS; MESODERM; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION;

EID: 33751197030     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2006-05-021386     Document Type: Article

References (86)

1. Baron MH. Early patterning of the mouse embryo: implications for hematopoietic commitment and differentiation. Exp Hematol. 2005;33:1015-1020.
2. McGrath KE, Palis J. Hematopoiesis in the yolk sac: more than meets the eye. Exp Hematol. 2005;33:1021-1028.
3. Dieterlen-Lievre F, Le Douarin NM. From the hemangioblast to self-tolerance: a series of innovations gained from studies on the avian embryo. Mech Dev. 2004;121:1117-1128.
4. Orkin SH, Zon LI. Hematopoiesis and stem cells: plasticity versus developmental heterogeneity. Nat Immunol. 2002;3:323-328.
5. Kondo M, Wagers AJ, Manz MG, et al. Biology of hematopoietic stem cells and progenitors: implications for clinical application. Annu Rev Immunol. 2003;21:759-806.
6. Dzierzak E. The emergence of definitive hematopoietic stem cells in the mammal. Curr Opin Hematol. 2005;12:197-202.
7. Psychoyos D, Stern CD. Fates and migratory routes of primitive streak cells in the chick embryo. Development. 1996;122:1523-1534.
8. Minko K, Bollerot K, Drevon C, Hallais MF, Jaffredo T. From mesoderm to blood islands: patterns of key molecules during yolk sac erythropoiesis. Gene Expr Patterns. 2003;3:261-272.
9. Garcia-Martinez V, Schoenwolf GC. Positional control of mesoderm movement and fate during avian gastrulation and neurulation. Dev Dyn. 1992;193:249-256.
10. Hsia N, Zon LI. Transcriptional regulation of hematopoietic stem cell development in zebrafish. Exp Hematol. 2005;33:1007-1014.
11. Park C, Ma YD, Choi K. Evidence for the hemangioblast. Exp Hematol. 2005;33:965-970.
12. Jaffredo T, Nottingham W, Liddiard K, Bollerot K, Pouget C, de Bruijn M. From hemangioblast to hematopoietic stem cell: an endothelial connection? Exp Hematol. 2005;33:1029-1040.
13. Lacaud G, Robertson S, Palis J, Kennedy M, Keller G. Regulation of hemangioblast development. Ann N Y Acad Sci. 2001;938:96-107; discussion 108.
14. Huber TL, Kouskoff V, Fehling HJ, Palis J, Keller G. Haemangioblast commitment is initiated in the primitive streak of the mouse embryo. Nature. 2004;432:625-630.
15. Nishikawa SI. A complex linkage in the developmental pathway of endothelial and hematopoietic cells. Curr Opin Cell Biol. 2001;13:673-678.
16. Kuo Z. Ontogeny of embryonic behavior in Aves, I: the chronology and general nature of the behavior of the chick embryo. J Exp Zool. 1932;61:395-430.
17. Pierce M. The amnion of the chick as an independent effector. J Exp Zool. 1933;65:443-473.
18. Sabin FR. Studies on the origin of blood-vessels and of red blood-corpuscles as seen in the living blastderm of chicks during the second day of incubation. Carnegie Inst Wash Publ Contribs Embryol. 1920;9:213-262.
19. Sabin FR. Origin and development of the primitive vessels of the chick and of the pig. Carnegie Inst Wash Publ Contribs Embryol. 1917;6:61-124.
20. Murray PDF. The development in vitro of the blood of the early chick embryo. Proc R Soc Lond B Biol Sci. 1932;11:497-521.
21. Wilt FH. The control of embryonic hemoglobin synthesis. Adv Morphog. 1967;6:89-125.
22. Ferkowicz MJ, Yoder MC. Blood island formation: longstanding observations and modern interpretations. Exp Hematol. 2005;33:1041-1047.
23. Bruns GA, Ingram VM. The erythroid cells and haemoglobins of the chick embryo. Philos Trans R Soc Lond B Biol Sci. 1973;266:225-305.
24. Ginder GD, Singal R, Little JA, Dempsey N, Ferris R, Wang SZ. Silencing and activation of embryonic globin gene expression. Ann N Y Acad Sci. 1998;850:70-79.
25. Evans T, Felsenfeld G, Reitman M. Control of globin gene transcription. Annu Rev Cell Biol. 1990;6:95-124.
26. Minie M, Clark D, Trainor C, et al. Developmental regulation of globin gene expression. J Cell Sci Suppl. 1992;16:15-20.
27. Sieweke MH, Graf T. A transcription factor party during blood cell differentiation. Curr Opin Genet Dev. 1998;8:545-551.
28. Engel I, Murre C. Transcription factors in hematopoiesis. Curr Opin Genet Dev. 1999;9:575-579.
29. Cantor AB, Orkin SH. Hematopoietic development: a balancing act. Curr Opin Genet Dev. 2001;11:513-519.
30. Walmsley M, Ciau-Uitz A, Patient R. Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus. Development. 2002;129:5683-5695.
31. Snyder A, Fraser ST, Baron MH. Bone morphogenetic proteins in vertebrate hematopoietic development. J Cell Biochem. 2004;93:224-232.
32. Schmerer M, Evans T. Primitive erythropoiesis is regulated by Smad-dependent signaling in postgastrulation mesoderm. Blood. 2003;102:3196-3205.
33. Drake CJ, LaRue A, Ferrara N, Little CD. VEGF regulates cell behavior during vasculogenesis. Dev Biol. 2000;224:178-188.
34. Shalaby F, Ho J, Stanford WL, et al. A requirement for Flk1 in primitive and definitive hematopoiesis and vasculogenesis. Cell. 1997;89:981-990.
35. Eichmann A, Corbel C, Nataf V, Vaigot P, Breant C, Le Douarin NM. Ligand-dependent development of the endothelial and hemopoietic lineages from embryonic mesodermal cells expressing vascular endothelial growth factor receptor 2. Proc Natl Acad Sci U S A. 1997;94:5141-5146.
36. Gerber HP, Malik AK, Solar GP, et al. VEGF regulates haematopoietic stem cell survival by an internal autocrine loop mechanism. Nature. 2002;417:954-958.
37. Van Den Berg DJ, Sharma AK, Bruno E, Hoffman R. Role of members of the Wnt gene family in human hematopoiesis. Blood. 1998;92:3189-3202.
38. Austin TW, Solar GP, Ziegler FC, Liem L, Matthews W. A role for the Wnt gene family in hematopoiesis: expansion of multilineage progenitor cells. Blood. 1997;89:3624-3635.
39. Shawber CJ, Kitajewski J. Notch function in the vasculature: insights from zebrafish, mouse and man. Bioessays. 2004;26:225-234.
40. Siatskas C, Boyd R. Regulation of chicken haemopoiesis by cytokines. Dev Comp Immunol. 2000;24:37-59.
41. Slack JM, Darlington BG, Heath JK, Godsave SF. Mesoderm induction in early Xenopus embryos by heparin-binding growth factors. Nature. 1987;326:197-200.
42. Yamaguchi TP, Harpal K, Henkemeyer M, Rossant J. fgfr-1 is required for embryonic growth and mesodermal patterning during mouse gastrulation. Genes Dev. 1994;8:3032-3044.
43. Sun X, Meyers EN, Lewandoski M, Martin GR. Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo. Genes Dev. 1999;13:1834-1846.
44. Furthauer M, Van Celst J, Thisse C, Thisse B. Fgf signalling controls the dorsoventral patterning of the zebrafish embryo. Development. 2004;131:2853-2864.
45. Griffin K, Patient R, Holder N. Analysis of FGF function in normal and no tail zebrafish embryos reveals separate mechanisms for formation of the trunk and the tail. Development. 1995;121:2983-2994.
46. Nutt SL, Dingwell KS, Holt CE, Amaya E. Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning. Genes Dev. 2001;15:1152-1166.
47. Yang X, Dormann D, Munsterberg AE, Weijer CJ. Cell movement patterns during gastrulation in the chick are controlled by positive and negative chemotaxis mediated by FGF4 and FGF8. Dev Cell. 2002;3:425-437.
48. Presta M, Dell'Era P, Mitola S, Moroni E, Ronca R, Rusnati M. Fibroblast growth factor/fibroblast growth factor receptor system in angiogenesis. Cytokine Growth Factor Rev. 2005;16:159-178.
49. Auguste P, Javerzat S, Bikfalvi A. Regulation of vascular development by fibroblast growth factors. Cell Tissue Res. 2003;314:157-166.
50. Moroni E, Dell'Era P, Rusnati M, Presta M. Fibroblast growth factors and their receptors in hematopoiesis and hematological tumors. J Hematother Stem Cell Res. 2002;11:19-32.
51. Gordon-Thomson C, Fabian BC. Hypoblastic tissue and fibroblast growth factor induce blood tissue (haemoglobin) in the early chick embryo. Development. 1994;120:3571-3579.
52. Huber TL, Zhou Y, Mead PE, Zon LI. Cooperative effects of growth factors involved in the induction of hematopoietic mesoderm. Blood. 1998;92:4128-4137.
53. Allouche M, Bikfalvi A. The role of fibroblast growth factor-2 (FGF-2) in hematopoiesis. Prog Growth Factor Res. 1995;6:35-48.
54. Xu RH, Ault KT, Kim J, et al. Opposite effects of FGF and BMP-4 on embryonic blood formation: roles of PV.1 and GATA-2. Dev Biol. 1999;208:352-361.
55. Bartunek P, Pajer P, Karafiat V, Blendinger G, Dvorak M, Zenke M. bFGF signaling and v-Myb cooperate in sustained growth of primitive erythroid progenitors. Oncogene. 2002;21:400-410.
56. Stern CD. Detection of multiple gene products simultaneously by in situ hybridization and immunohistochemistry in whole mounts of avian embryos. Curr Top Dev Biol. 1998;36:223-243.
57. Shin M, Watanuki K, Yasugi S. Expression of Fgf10 and Fgf receptors during development of the embryonic chicken stomach. Gene Expr Patterns. 2005;5:511-516.
58. Webster MK, Donoghue DJ. Enhanced signaling and morphological transformation by a membrane-localized derivative of the fibroblast growth factor receptor 3 kinase domain. Mol Cell Biol. 1997;17:5739-5747.
59. Niwa H, Yamamura K, Miyazaki J. Efficient selection for high-expression transfectants with a novel eukaryotic vector. Gene. 1991;108:193-199.
60. Palis J, McGrath KE, Kingsley PD. Initiation of hematopoiesis and vasculogenesis in murine yolk sac explants. Blood. 1995;86:156-163.
61. Worthington RE, Bossie-Codreanu J, Van Zant G. Quantitation of erythroid differentiation in vitro using a sensitive colorimetric assay for hemoglobin. Exp Hematol. 1987;15:85-92.
62. Wilt FH. The beginnings of erythropoiesis in the yolk sac of the chick embryo. Ann N Y Acad Sci. 1974;241:99-112.
63. Wainwright SD, Wainwright LK. A kinetic study of the effects of delta-aminolevulinic acid upon the synthesis of embryonic and fetal hemoglobins in the blood islands of the developing chick blastodisc. Can J Biochem. 1970;48:400-406.
64. Silver L, Palis J. Initiation of murine embryonic erythropoiesis: a spatial analysis. Blood. 1997;89:1154-1164.
65. Eichmann A, Marcelle C, Breant C, Le Douarin NM. Two molecules related to the VEGF receptor are expressed in early endothelial cells during avian embryonic development. Mech Dev. 1993;42:33-48.
66. Tahtakran SA, Selleck MA. Ets-1 expression is associated with cranial neural crest migration and vasculogenesis in the chick embryo. Gene Expr Patterns. 2003;3:455-458.
67. Mohammadi M, McMahon G, Sun L, et al. Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science. 1997;276:955-960.
68. Stern CD, Ireland GW. An integrated experimental study of endoderm formation in avian embryos. Anat Embryol (Berl). 1981;163:245-263.
69. Walshe J, Mason I. Expression of FGFR1, FGFR2 and FGFR3 during early neural development in the chick embryo. Mech Dev. 2000;90:103-110.
70. Xu X,Weinstein M, Li C, et al. Fibroblast growth factor receptor 2 (FGFR2)-mediated reciprocal regulation loop between FGF8 and FGF10 is essential for limb induction. Development. 1998;125:753-765.
71. Fong TA, Shawver LK, Sun L, et al. SU5416 is a potent and selective inhibitor of the vascular endothelial growth factor receptor (Flk-1/KDR) that inhibits tyrosine kinase catalysis, tumor vascularization, and growth of multiple tumor types. Cancer Res. 1999;59:99-106.
72. Cross LM, Cook MA, Lin S, Chen JN, Rubinstein AL. Rapid analysis of angiogenesis drugs in a live fluorescent zebrafish assay. Arterioscler Thromb Vasc Biol. 2003;23:911-912.
73. Palis J, Robertson S, Kennedy M, Wall C, Keller G. Development of erythroid and myeloid progenitors in the yolk sac and embryo proper of the mouse. Development. 1999;126:5073-5084.
74. Dieterlen-Lievre F, Beaupain D, Martin C. Origin of erythropoietic stem cells in avian development: shift from the yolk sac to an intraembryonic site. Ann Immunol (Paris). 1976;127:857-863.
75. Poole TJ, Finkelstein EB, Cox CM. The role of FGF and VEGF in angioblast induction and migration during vascular development. Dev Dyn. 2001;220:1-17.
76. Jih YJ, Lien WH, Tsai WC, Yang GW, Li C, Wu LW. Distinct regulation of genes by bFGF and VEGF-A in endothelial cells. Angiogenesis. 2001;4:313-321.
77. Nico B, de Falco G, Vacca A, Roncali L, Ribatti D. In vivo absence of synergism between fibroblast growth factor-2 and vascular endothelial growth factor. J Hematother Stem Cell Res. 2001;10:905-912.
78. Welch JJ, Watts JA, Vakoc CR, et al. Global regulation of erythroid gene expression by transcription factor GATA-1. Blood. 2004;104:3136-3147.
79. McDevitt MA, Shivdasani RA, Fujiwara Y, Yang H, Orkin SH. A "knockdown" mutation created by cis-element gene targeting reveals the dependence of erythroid cell maturation on the level of transcription factor GATA-1. Proc Natl Acad Sci U S A. 1997;94:6781-6785.
80. Flamme I, Risau W. Induction of vasculogenesis and hematopoiesis in vitro. Development. 1992;116:435-439.
81. Delfini MC, Dubrulle J, Malapert P, Chal J, Pourquie O. Control of the segmentation process by graded MAPK/ERK activation in the chick embryo. Proc Natl Acad Sci U S A. 2005;102:11343-11348.
82. Eswarakumar VP, Lax I, Schlessinger J. Cellular signaling by fibroblast growth factor receptors. Cytokine Growth Factor Rev. 2005;16:139-149.
83. Dubrulle J, Pourquie O. fgf8 mRNA decay establishes a gradient that couples axial elongation to patterning in the vertebrate embryo. Nature. 2004;427:419-422.
84. Karabagli H, Karabagli P, Ladher RK, Schoenwolf GC. Comparison of the expression patterns of several fibroblast growth factors during chick gastrulation and neurulation. Anat Embryol (Berl). 2002;205:365-370.
85. Wright TJ, Ladher R, McWhirter J, Murre C, Schoenwolf GC, Mansour SL. Mouse FGF15 is the ortholog of human and chick FGF19, but is not uniquely required for otic induction. Dev Biol. 2004;269:264-275.
86. Olsen SK, Li JY, Bromleigh C, et al. Structural basis by which alternative splicing modulates the organizer activity of FGF8 in the brain. Genes Dev. 2006;20:185-198.