Maintenance of HSC by Wnt5a secreting AGM-derived stromal cell line

Experimental Hematology

Volumn 39, Issue 1, 2011, Pages

  Buckley, Shannon M ^a,b   Ulloa Montoya, Fernando ^a,b   Abts, David ^b   Oostendorp, Robert A J ^c   Dzierzak, Elaine ^d   Ekker, Stephen C ^e   Verfaillie, Catherine M ^a,b  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^d ERASMUS MEDICAL CENTER   (Netherlands)

^e MAYO CLINIC CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

WNT5A PROTEIN;

ANIMAL CELL; AORTA; ARTICLE; BONE MARROW CELL; CELL CULTURE; CELL DIFFERENTIATION; CELL FATE; CELL RENEWAL; CONTROLLED STUDY; EMBRYO; FEMALE; GENE EXPRESSION; GONAD; HEMATOPOIETIC STEM CELL; LIVER; MESONEPHROS; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN SECRETION; STROMA CELL;

MURINAE;

EID: 78650205344     PISSN: 0301472X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.exphem.2010.09.010     Document Type: Article

References (61)

1. Calvi L.M., Adams G.B., Weibrecht K.W., et al. Osteoblastic cells regulate the haematopoietic stem cell niche. Nature 2003, 425:841-846.
2. Fleming H.E., Janzen V., Lo Celso C., et al. Wnt signaling in the niche enforces hematopoietic stem cell quiescence and is necessary to preserve self-renewal in vivo. Cell Stem Cell 2008, 2:274-283.
3. Hackney J.A., Charbord P., Brunk B.P., Stoeckert C.J., Lemischka I.R., Moore K.A. A molecular profile of a hematopoietic stem cell niche. Proc Natl Acad Sci U S A 2002, 99:13061-13066.
4. Wilson A., Trumpp A. Bone-marrow haematopoietic-stem-cell niches. Nat Rev 2006, 6:93-106.
5. Zhang J., Niu C., Ye L., et al. Identification of the haematopoietic stem cell niche and control of the niche size. Nature 2003, 425:836-841.
6. Baron M.H. Embryonic origins of mammalian hematopoiesis. Exp Hematol 2003, 31:1160-1169.
7. Baron M.H., Fraser S.T. The specification of early hematopoiesis in the mammal. Curr Opin Hematol 2005, 12:217-221.
8. Dzierzak E. The emergence of definitive hematopoietic stem cells in the mammal. Curr Opin Hematol 2005, 12:197-202.
9. Dzierzak E. Embryonic beginnings of definitive hematopoietic stem cells. Ann N Y Acad Sci 1999, 872:256-262. discussion 262-254.
10. Dzierzak E., Medvinsky A. Mouse embryonic hematopoiesis. Trends Genet 1995, 11:359-366.
11. Mikkola H.K., Gekas C., Orkin S.H., Dieterlen-Lievre F. Placenta as a site for hematopoietic stem cell development. Exp Hematol 2005, 33:1048-1054.
12. Miller C.L., Eaves C.J. Expansion in vitro of adult murine hematopoietic stem cells with transplantable lympho-myeloid reconstituting ability. Proc Natl Acad Sci U S A 1997, 94:13648-13653.
13. Zhang C.C., Kaba M., Ge G., et al. Angiopoietin-like proteins stimulate ex vivo expansion of hematopoietic stem cells. Nat Med 2006, 12:240-245.
14. Zhang C.C., Lodish H.F. Insulin-like growth factor 2 expressed in a novel fetal liver cell population is a growth factor for hematopoietic stem cells. Blood 2004, 103:2513-2521.
15. Ueda T., Tsuji K., Yoshino H., et al. Expansion of human NOD/SCID-repopulating cells by stem cell factor, Flk2/Flt3 ligand, thrombopoietin, IL-6, and soluble IL-6 receptor. J Clin Invest 2000, 105:1013-1021.
16. Palis J., Yoder M.C. Yolk-sac hematopoiesis: the first blood cells of mouse and man. Exp Hematol 2001, 29:927-936.
17. 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.
18. 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.
19. Yoder M.C., Hiatt K., Mukherjee P. In vivo repopulating hematopoietic stem cells are present in the murine yolk sac at day 9.0 postcoitus. Proc Natl Acad Sci U S A 1997, 94:6776-6780.
20. Morrison S.J., Hemmati H.D., Wandycz A.M., Weissman I.L. The purification and characterization of fetal liver hematopoietic stem cells. Proc Natl Acad Sci U S A 1995, 92:10302-10306.
21. Medvinsky A.L., Dzierzak E.A. Development of the definitive hematopoietic hierarchy in the mouse. Dev Comp Imunol 1998, 22:289-301.
22. Blanpain C., Fuchs E. Epidermal stem cells of the skin. Annu Rev Cell Dev Biol 2006, 22:339-373.
23. Yen T.H., Wright N.A. The gastrointestinal tract stem cell niche. Stem Cell Rev 2006, 2:203-212.
24. Kiger A.A., Jones D.L., Schulz C., Rogers M.B., Fuller M.T. Stem cell self-renewal specified by JAK-STAT activation in response to a support cell cue. Science 2001, 294:2542-2545.
25. Song X., Call G.B., Kirilly D., Xie T. Notch signaling controls germline stem cell niche formation in the Drosophila ovary. Development 2007, 134:1071-1080.
26. Song X., Wong M.D., Kawase E., et al. Bmp signals from niche cells directly repress transcription of a differentiation-promoting gene, bag of marbles, in germline stem cells in the Drosophila ovary. Development 2004, 131:1353-1364.
27. Tulina N., Matunis E. Control of stem cell self-renewal in Drosophila spermatogenesis by JAK-STAT signaling. Science 2001, 294:2546-2549.
28. Oostendorp R.A., Harvey K.N., Kusadasi N., et al. Stromal cell lines from mouse aorta-gonads-mesonephros subregions are potent supporters of hematopoietic stem cell activity. Blood 2002, 99:1183-1189.
29. Dexter T.M., Allen T.D., Lajtha L.G. Conditions controlling the proliferation of haemopoietic stem cells in vitro. J Cell Physiol 1977, 91:335-344.
30. Moore K.A., Ema H., Lemischka I.R. In vitro maintenance of highly purified, transplantable hematopoietic stem cells. Blood 1997, 89:4337-4347.
31. Harvey K., Dzierzak E. Cell-cell contact and anatomical compatibility in stromal cell-mediated hsc support during development. Stem Cells 2004, 22:253-258.
32. Oostendorp R.A., Medvinsky A.J., Kusadasi N., et al. Embryonal subregion-derived stromal cell lines from novel temperature-sensitive SV40 T antigen transgenic mice support hematopoiesis. J Cell Sci 2002, 115:2099-2108.
33. Kusadasi N., Oostendorp R.A., Koevoet W.J., Dzierzak E.A., Ploemacher R.E. Stromal cells from murine embryonic aorta-gonad-mesonephros region, liver and gut mesentery expand human umbilical cord blood-derived CAFC(week6) in extended long-term cultures. Leukemia 2002, 16:1782-1790.
34. 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 U S A 2007, 104:20838-20843.
35. Durand C., Robin C., Dzierzak E. Mesenchymal lineage potentials of aorta-gonad-mesonephros stromal clones. Haematologica 2006, 91:1172-1179.
36. Austin T.W., Solar G.P., Ziegler F.C., Liem L., Matthews W. A role for the Wnt gene family in hematopoiesis: expansion of multilineage progenitor cells. Blood 1997, 89:3624-3635.
37. Van Den Berg D.J., Sharma A.K., Bruno E., Hoffman R. Role of members of the Wnt gene family in human hematopoiesis. Blood 1998, 92:3189-3202.
38. Brandon C., Eisenberg L.M., Eisenberg C.A. WNT signaling modulates the diversification of hematopoietic cells. Blood 2000, 96:4132-4141.
39. van de Wetering M., de Lau W., Clevers H. WNT signaling and lymphocyte development. Cell 2002, 109(suppl):S13-S19.
40. Reya T., Duncan A.W., Ailles L., et al. A role for Wnt signalling in self-renewal of haematopoietic stem cells. Nature 2003, 423:409-414.
41. Zhao R.C., Jiang Y., Verfaillie C.M. A model of human p210(bcr/ABL)-mediated chronic myelogenous leukemia by transduction of primary normal human CD34(+) cells with a BCR/ABL-containing retroviral vector. Blood 2001, 97:2406-2412.
42. Ema H., Morita Y., Yamazaki S., et al. Adult mouse hematopoietic stem cells: purification and single-cell assays. Nat Protoc 2006, 1:2979-2987.
43. Verfaillie C.M. Direct contact between human primitive hematopoietic progenitors and bone marrow stroma is not required for long-term in vitro hematopoiesis. Blood 1992, 79:2821-2826.
44. Harrison D.E. Competitive repopulation: a new assay for long-term stem cell functional capacity. Blood 1980, 55:77-81.
45. Harrison D.E., Jordan C.T., Zhong R.K., Astle C.M. Primitive hemopoietic stem cells: direct assay of most productive populations by competitive repopulation with simple binomial, correlation and covariance calculations. Exp Hematol 1993, 21:206-219.
46. Szilvassy S.J., Humphries R.K., Lansdorp P.M., Eaves A.C., Eaves C.J. Quantitative assay for totipotent reconstituting hematopoietic stem cells by a competitive repopulation strategy. Proc Natl Acad Sci U S A 1990, 87:8736-8740.
47. Oostendorp R.A., Robin C., Steinhoff C., et al. Long-term maintenance of hematopoietic stem cells does not require contact with embryo-derived stromal cells in cocultures. Stem Cells 2005, 23:842-851.
48. Gordon M.D., Nusse R. Wnt signaling: multiple pathways, multiple receptors, and multiple transcription factors. J Biol Chem 2006, 281:22429-22433.
49. Mikels A.J., Nusse R. Purified Wnt5a protein activates or inhibits beta-catenin-TCF signaling depending on receptor context. PLoS Biol 2006, 4:e115.
50. Zhong J.F., Zhao Y., Sutton S., et al. Gene expression profile of murine long-term reconstituting vs. short-term reconstituting hematopoietic stem cells. Proc Natl Acad Sci U S A 2005, 102:2448-2453.
51. Osawa M., Hanada K., Hamada H., Nakauchi H. Long-term lymphohematopoietic reconstitution by a single CD34-low/negative hematopoietic stem cell. Science 1996, 273:242-245.
52. Muller A.M., Medvinsky A., Strouboulis J., Grosveld F., Dzierzak E. Development of hematopoietic stem cell activity in the mouse embryo. Immunity 1994, 1:291-301.
53. Thiemann F.T., Moore K.A., Smogorzewska E.M., Lemischka I.R., Crooks G.M. The murine stromal cell line AFT024 acts specifically on human CD34+CD38- progenitors to maintain primitive function and immunophenotype in vitro. Exp Hematol 1998, 26:612-619.
54. Khan N.I., Bendall L.J. Role of WNT signaling in normal and malignant hematopoiesis. Histol Histopathol 2006, 21:761-774.
55. Kirstetter P., Anderson K., Porse B.T., Jacobsen S.E., Nerlov C. Activation of the canonical Wnt pathway leads to loss of hematopoietic stem cell repopulation and multilineage differentiation block. Nat Immunol 2006, 7:1048-1056.
56. Murdoch B., Chadwick K., Martin M., et al. Wnt-5A augments repopulating capacity and primitive hematopoietic development of human blood stem cells in vivo. Proc Natl Acad Sci U S A 2003, 100:3422-3427.
57. Yamaguchi T.P., Bradley A., McMahon A.P., Jones S. A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo. Development 1999, 126:1211-1223.
58. Chen Y., Haviernik P., Bunting K.D., Yang Y.C. Cited2 is required for normal hematopoiesis in the murine fetal liver. Blood 2007, 110:2889-2898.
59. Chen D., Wang P., Lewis R.L., et al. A microarray analysis of the emergence of embryonic definitive hematopoiesis. Exp Hematol 2007, 35:1344-1357.
60. Schuringa J.J., Wu K., Morrone G., Moore M.A. Enforced activation of STAT5A facilitates the generation of embryonic stem-derived hematopoietic stem cells that contribute to hematopoiesis in vivo. Stem Cells 2004, 22:1191-1204.
61. Nemeth M.J., Topol L., Anderson S.M., Yang Y., Bodine D.M. Wnt5a inhibits canonical Wnt signaling in hematopoietic stem cells and enhances repopulation. Proc Natl Acad Sci U S A 2007, 104:15436-15441.