Cell interactions and cell signaling during hematopoietic development

Experimental Cell Research

Volumn 329, Issue 2, 2014, Pages 200-206

  Drevon, C ^a,b   Jaffredo, T ^a,b  

^a SORBONNE UNIVERSITÉ   (France)

^b Sorbonne Universités   (France)

Author keywords

Aorta; Chicken; Chimeras; Development; Endoderm; Endothelium; Hematopoietic stem cells; Mouse; Notch; Quail

Indexed keywords

BONE MORPHOGENETIC PROTEIN; TRANSCRIPTION FACTOR RUNX1; TRANSFORMING GROWTH FACTOR BETA;

CELL INTERACTION; ENDODERM; ENDOTHELIUM CELL; GENE EXPRESSION; HEMANGIOBLAST; HEMATOPOIESIS; HEMATOPOIETIC CELL; HEMATOPOIETIC STEM CELL; HUMAN; IN VITRO STUDY; IN VIVO STUDY; MESODERM; NONHUMAN; NOTOCHORD; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; REVIEW; SIGNAL TRANSDUCTION; TISSUE INTERACTION; ADULT; ANIMAL; CELL COMMUNICATION; CELL DIFFERENTIATION; CELL FUNCTION; CYTOLOGY; PHYSIOLOGY;

PHASIANIDAE;

ADULT; ANIMALS; CELL COMMUNICATION; CELL DIFFERENTIATION; CELL PHYSIOLOGICAL PHENOMENA; HEMATOPOIESIS; HEMATOPOIETIC STEM CELLS; HUMANS; SIGNAL TRANSDUCTION;

EID: 84922482273     PISSN: 00144827     EISSN: 10902422     Source Type: Journal    
DOI: 10.1016/j.yexcr.2014.10.009     Document Type: Review

References (52)

1. 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.
2. Sheng G. Primitive and definitive erythropoiesis in the yolk sac: a bird's eye view. Int. J. Dev. Biol. 2010, 54:1033-1043.
3. Minko K., Bollerot K., Drevon C., Hallais M.F., Jaffredo T. From mesoderm to blood islands: patterns of key molecules during yolk sac erythropoiesis. Gene Expr. Patterns 2003, 3:261-272.
4. Boiers C., Carrelha J., Lutteropp M., Luc S., Green J.C., Azzoni E., Woll P.S., Mead A.J., Hultquist A., Swiers G., Perdiguero E.G., Macaulay I.C., Melchiori L., Luis T.C., Kharazi S., Bouriez-Jones T., Deng Q., Ponten A., Atkinson D., Jensen C.T., Sitnicka E., Geissmann F., Godin I., Sandberg R., de Bruijn M.F., Jacobsen S.E. Lymphomyeloid contribution of an immune-restricted progenitor emerging prior to definitive hematopoietic stem cells. Cell Stem Cell 2013, 13:1-14.
5. Guedes P.T., de Oliveira B.C., Manso P.P., Caputo L.F., Cotta-Pereira G., Pelajo-Machado M. Histological analyses demonstrate the temporary contribution of yolk sac, liver, and bone marrow to hematopoiesis during chicken development. PLoS One 2014, 9:e90975.
6. Chen M.J., Li Y., De Obaldia M.E., Yang Q., Yzaguirre A.D., Yamada-Inagawa T., Vink C.S., Bhandoola A., Dzierzak E., Speck N.A. Erythroid/myeloid progenitors and hematopoietic stem cells originate from distinct populations of endothelial cells. Cell Stem Cell 2011, 9:541-552.
7. Sabin F.R. Studies on the origin of blood vessels and of red corpuscles as seen in the living blastoderm of the chick during the second day of incubation. Contrib. Embryol. 1920, 9:213-262.
8. Murray P.D.F. The development in vitro of blood of the early chick embryo. Strangeways Res. Lab. Cambridge 1932, 497-521.
9. Choi K., Kennedy M., Kazarov A., Papadimitriou J.C., Keller G. A common precursor for hematopoietic and endothelial cells. Development 1998, 125:725-732.
10. Kennedy M., Firpo M., Choi K., Wall C., Robertson S., Kabrun N., Keller G. A common precursor for primitive erythropoiesis and definitive haematopoiesis. Nature 1997, 386:488-493.
11. Shalaby F., Ho J., Stanford W.L., Fischer K.-D., Schuh A., Schwartz L., Bernstein A., Rossant J. A requirement for flk-1 in primitive and definitive hematopoiesis and vasculogenesis. Cell 1997, 89:981-990.
12. Shalaby F., Rossant J., Yamaguchi T.P., Gertsenstein M., Wu X.-F., Breitman M.L., Schuh A.C. Failure of blood-island formation and vasculogenesis in Flk-1-deficient mice. Nature 1995, 376:62-66.
13. Dumont D.J., Gradwohl G., Fong G.H., Puri M.C., Gertsenstein M., Auerbach A., Breitman M.L. Dominant-negative and targeted null mutations in the endothelial receptor tyrosine kinase, tek, reveal a critical role in vasculogenesis of the embryo. Genes Dev. 1994, 8:1897-1909.
14. Takakura N., Huang X.L., Naruse T., Hamaguchi I., Dumont D.J., Yancopoulos G.D., Suda T. Critical role of the TIE2 endothelial cell receptor in the development of definitive hematopoiesis. Immunity 1998, 9:677-686.
15. Jaffredo T., Gautier R., Brajeul V., Dieterlen-Lievre F. Tracing the progeny of the aortic hemangioblast in the avian embryo. Dev. Biol. 2000, 224:204-214.
16. Jaffredo T., Gautier R., Eichmann A., Dieterlen-Lievre F. Intraaortic hemopoietic cells are derived from endothelial cells during ontogeny. Development 1998, 125:4575-4583.
17. Zovein A.C., Hofmann J.J., Lynch M., French W.J., Turlo K.A., Yang Y., Becker M.S., Zanetta L., Dejana E., Gasson J.C., Tallquist M.D., Iruela-Arispe M.L. Fate tracing reveals the endothelial origin of hematopoietic stem cells. Cell Stem Cell 2008, 3:625-636.
18. Chen M.J., Yokomizo T., Zeigler B.M., Dzierzak E., Speck N.A. Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter. Nature 2009, 457:887-891.
19. de Bruijn M., Ma X., Robin C., Ottersbach K., Sanchez M.J., Dzierzak E. Hematopoietic stem cells localise to the endothelial cell layer in the midgestation mouse aorta. Immunity 2002, 16:673-683.
20. Eilken H.M., Nishikawa S., Schroeder T. Continuous single-cell imaging of blood generation from haemogenic endothelium. Nature 2009, 457:896-900.
21. Lancrin C., Sroczynska P., Stephenson C., Allen T., Kouskoff V., Lacaud G. The haemangioblast generates haematopoietic cells through a haemogenic endothelium stage. Nature 2009, 457:892-895.
22. Kissa K., Herbomel P. Blood stem cells emerge from aortic endothelium by a novel type of cell transition. Nature 2010, 464:112-115.
23. Bertrand J.Y., Chi N.C., Santoso B., Teng S., Stainier D.Y., Traver D. Haematopoietic stem cells derive directly from aortic endothelium during development. Nature 2010, 464:108-111.
24. Lam E.Y., Hall C.J., Crosier P.S., Crosier K.E., Flores M.V. Live imaging of Runx1 expression in the dorsal aorta tracks the emergence of blood progenitors from endothelial cells. Blood 2010, 116:909-914.
25. Boisset J.C., van Cappellen W., Andrieu-Soler C., Galjart N., Dzierzak E., Robin C. In vivo imaging of haematopoietic cells emerging from the mouse aortic endothelium. Nature 2010, 464:116-120.
26. Wilt F.H. Erythropoiesis in the chick embryo: the role of the endoderm. Science 1965, 147:1588-1590.
27. Kessel J., Fabian B. Inhibitory and stimulatory influences on mesodermal erythropoiesis in the early chick blastoderm. Development 1987, 101:45-49.
28. Gordon-Thomson C., Fabian B.C. Hypoblastic tissue and fibroblast growth factor induce blood tissue (haemoglobin) in the early chick embryo. Development 1994, 120:3571-3579.
29. Dyer M.A., Farrington S.M., Mohn D., Munday J.R., Baron M.H. Indian hedgehog activates hematopoiesis and vasculogenesis and can respecify prospective neurectodermal cell fate in the mouse embryo. Development 2001, 128:1717-1730.
30. Giles P.B., Candy C.L., Fleming P.A., Owens R.W., Argraves W.S., Drake C.J. VEGF directs newly gastrulated mesoderm to the endothelial lineage. Dev. Biol. 2005, 279:169-178.
31. Gottgens B., Nastos A., Kinston S., Piltz S., Delabesse E.C., Stanley M., Sanchez M.J., Ciau-Uitz A., Patient R., Green A.R. Establishing the transcriptional programme for blood: the SCL stem cell enhancer is regulated by a multiprotein complex containing Ets and GATA factors. EMBO J. 2002, 21:3039-3050.
32. Liu F., Walmsley M., Rodaway A., Patient R. Fli1 acts at the top of the transcriptional network driving blood and endothelial development. Curr. Biol. 2008, 18:1234-1240.
33. Ciau-Uitz A., Wang L., Patient R., Liu F. ETS transcription factors in hematopoietic stem cell development. Blood Cells Mol. Dis. 2013, 51:248-255.
34. Richard C., Drevon C., Canto P.Y., Villain G., Bollerot K., Lempereur A., Teillet M.A., Vincent C., Rossello Castillo C., Torres M., Piwarzyk E., Speck N.A., Souyri M., Jaffredo T. Endothelio-mesenchymal interaction controls runx1 expression and modulates the notch pathway to initiate aortic hematopoiesis. Dev. Cell 2013, 24:600-611.
35. Pardanaud L., Dieterlen-Lievre F. Manipulation of the angiopoietic/hemangiopoietic commitment in the avian embryo. Development 1999, 126:617-627.
36. Vokes S.A., Yatskievych T.A., Heimark R.L., McMahon J., McMahon A.P., Antin P.B., Krieg P.A. Hedgehog signaling is essential for endothelial tube formation during vasculogenesis. Development 2004, 131:4371-4380.
37. Peeters M., Ottersbach K., Bollerot K., Orelio C., de Bruijn M., Wijgerde M., Dzierzak E. Ventral embryonic tissues and hedgehog proteins induce early AGM hematopoietic stem cell development. Development 2009, 136:2613-2621.
38. Swiers G., Rode C., Azzoni E., de Bruijn M.F. A short history of hemogenic endothelium. Blood Cells Mol. Dis. 2013, 51:206-212.
39. North T., Gu T.L., Stacy T., Wang Q., Howard L., Binder M., Marin-Padilla M., Speck N.A. Cbfa2 is required for the formation of intra-aortic hematopoietic clusters. Development 1999, 126:2563-2575.
40. North T.E., de Bruijn M.F., Stacy T., Talebian L., Lind E., Robin C., Binder M., Dzierzak E., Speck N.A. Runx1 expression marks long-term repopulating hematopoietic stem cells in the midgestation mouse embryo. Immunity 2002, 16:661-672.
41. Gering M., Patient R. Notch signalling and haematopoietic stem cell formation during embryogenesis. J. Cell Physiol. 2010, 222:11-16.
42. Bigas A., Espinosa L. Hematopoietic stem cells: to be or Notch to be. Blood 2012, 119:3226-3235.
43. Robert-Moreno A., Espinosa L., de la Pompa J.L., Bigas A. RBPj{kappa}-dependent Notch function regulates Gata2 and is essential for the formation of intra-embryonic hematopoietic cells. Development 2005, 132:1117-1126.
44. Bigas A., Guiu J., Gama-Norton L. Notch and Wnt signaling in the emergence of hematopoietic stem cells. Blood Cells Mol. Dis. 2013, 51:264-270.
45. Robert-Moreno A., Espinosa L., Sanchez M.J., de la Pompa J.L., Bigas A. The notch pathway positively regulates programmed cell death during erythroid differentiation. Leukemia 2007, 21:1496-1503.
46. Lorsbach R.B., Moore J., Ang S.O., Sun W., Lenny N., Downing J.R. Role of RUNX1 in adult hematopoiesis: analysis of RUNX1-IRES-GFP knock-in mice reveals differential lineage expression. Blood 2004, 103:2522-2529.
47. Wilkinson R.N., Pouget C., Gering M., Russell A.J., Davies S.G., Kimelman D., Patient R. Hedgehog and Bmp polarize hematopoietic stem cell emergence in the zebrafish dorsal aorta. Dev. Cell 2009, 16:909-916.
48. Durand C., Robin C., Bollerot K., Baron M.H., Ottersbach K., Dzierzak E. Embryonic stromal clones reveal developmental regulators of definitive hematopoietic stem cells. Proc. Natl Acad. Sci. USA 2007, 104:20838-20843.
49. Marshall C.J., Kinnon C., Thrasher A.J. Polarized expression of bone morphogenetic protein-4 in the human aorta-gonad-mesonephros region. Blood 2000, 96:1591-1593.
50. Guo X., Wang X.F. Signaling cross-talk between TGF-beta/BMP and other pathways. Cell Res. 2009, 19:71-88.
51. Pimanda J.E., Donaldson I.J., de Bruijn M.F., Kinston S., Knezevic K., Huckle L., Piltz S., Landry J.R., Green A.R., Tannahill D., Gottgens B. The SCL transcriptional network and BMP signaling pathway interact to regulate RUNX1 activity. Proc. Nat. Acad. Sci. USA 2007, 104:840-845.
52. Goumans M.J., Valdimarsdottir G., Itoh S., Rosendahl A., Sideras P., ten Dijke P. Balancing the activation state of the endothelium via two distinct TGF-beta type I receptors. EMBO J. 2002, 21:1743-1753.