The symmetry of initial divisions of human hematopoietic progenitors is altered only by the cellular microenvironment

Experimental Hematology

Volumn 31, Issue 4, 2003, Pages 339-347

  Punzel, Michael ^a   Liu, Daihong ^a   Zhang, Tao ^a   Eckstein, Volker ^a   Miesala, Katrin ^a   Ho, Anthony D ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CD34 ANTIGEN; CD38 ANTIGEN; FIBRONECTIN; SERUM ALBUMIN;

ARTICLE; BONE MARROW CELL; CELL ASSAY; CELL CULTURE; CELL CYCLE; CELL DIVISION; CELL FUNCTION; CELL POPULATION; COLONY FORMING CELL; CONTROLLED STUDY; HEMATOPOIETIC STEM CELL; HUMAN; HUMAN CELL; LYMPHOID CELL; MICROSCOPY; PRIORITY JOURNAL; STEM CELL;

BOVINAE;

EID: 0037385037     PISSN: 0301472X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0301-472X(03)00024-9     Document Type: Article

References (50)

1. Morrison S.J., Shah N.M., Anderson D.J. Regulatory mechanisms in stem cell biology. Cell. 88:1997;287-298.
2. Wagers A.J., Christensen J.L., Weissman I.L. Cell fate determination from stem cells. Gene Ther. 9:2002;606-612.
3. Knoblich J.A. Asymmetric cell division during animal development. Nat Rev Mol Cell Biol. 2:2001;11-20.
4. Huang S., Law P., Francis K., Palsson B.O., Ho A.D. Symmetry of initial cell divisions among primitive hematopoietic progenitors is independent of ontogenic age and regulatory molecules. Blood. 94:1999;2595-2604.
5. - cells. Exp Hematol. 30:2002;464-472.
6. Gumbiner B.M. Cell adhesion. the molecular basis of tissue architecture and morphogenesis Cell. 84:1996;345-357.
7. Rosendaal M., Krenacs T.T. Regulatory pathways in blood-forming tissue with particular reference to gap junctional communication. Pathol Oncol Res. 6:2000;243-249.
8. Prosper F., Verfaillie C.M. Regulation of hematopoiesis through adhesion receptors. J Leukoc Biol. 69:2001;307-316.
9. Wagers A.J., Christensen J.L., Weissman I.L. Cell fate determination from stem cells. Gene Ther. 9:2002;606-612.
10. Zandstra P.W., Lauffenburger D.A., Eaves C.J. A ligand-receptor signaling threshold model of stem cell differentiation control. a biologically conserved mechanism applicable to hematopoiesis Blood. 96:2000;1215-1222.
11. Spradling A., Drummond-Barbosa D., Kai T. Stem cells find their niche. Nature. 414:2001;98-104.
12. Verfaillie C.M., Gupta P., Prosper F., Hurley R., Lundell B., Bhatia R. The hematopoietic microenvironment. stromal extracellular matrix components as growth regulators for human hematopoietic progenitors Hematology. 4:1999;321-333.
13. Wolf N.S. The hematopoietic microenvironment. stromal cell types: characterization and function in situ and in vitro Hematology. 4:1999;241-254.
14. Olesen G., Tonder H., Holm M.S., Hokland P. Long-term culture of hematopoietic stem cells - validating the stromal component of the CAFC assay. Cytotherapy. 3:2001;107-116.
15. Okubo T., Matsui N., Yanai N., Obinata M. Stroma-dependent maintenance of cytokine responsive hematopoietic progenitor cells derived from long-term bone marrow culture. Cell Struct Funct. 25:2000;133-139.
16. Punzel M., Moore K.A., Lemischka I.R., Verfaillie C.M. The type of stromal feeder used in limiting dilution assays influences frequency and maintenance assessment of human long-term culture initiating cells. Leukemia. 13:1999;92-97.
17. Nolta J.A., Thiemann F.T., Arakawa-Hoyt J.et al. The AFT024 stromal cell line supports long-term ex vivo maintenance of engrafting multipotent human hematopoietic progenitors. Leukemia. 16:2002;352-361.
18. Lewis I.D., Verfaillie C.M. Multi-lineage expansion potential of primitive hematopoietic progenitors. superiority of umbilical cord blood compared to mobilized peripheral blood Exp Hematol. 28:2000;1087-1095.
19. - progenitors to maintain primitive function and immunophenotype in vitro. Exp Hematol. 26:1998;612-619.
20. Moore K.A., Ema H., Lemischka I.R. In vitro maintenance of highly purified, transplantable hematopoietic stem cells. Blood. 89:1997;4337-4347.
21. Moore K.A., Pytowski B., Witte L., Hicklin D., Lemischka I.R. Hematopoietic activity of a stromal cell transmembrane protein containing epidermal growth factor-like repeat motifs. Proc Natl Acad Sci U S A. 94:1997;4011-4016.
22. 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. 99:2002;13061-13066.
23. Punzel M., Gupta P., Roodell M., Mortari F., Verfaillie C.M. Factor(s) secreted by AFT024 fetal liver cells following stimulation with human cytokines are important for human LTC-IC growth. Leukemia. 13:1999;1079-1084.
24. - progenitors give rise to natural killer cells, B-lineage cells, dendritic cells, and myeloid cells. Blood. 93:1999;96-106.
25. Punzel M., Wissink S.D., Miller J.S., Moore K.A., Lemischka I.R., Verfaillie C.M. The myeloid-lymphoid initiating cell (ML-IC) assay assesses the fate of multipotent human progenitors in vitro. Blood. 93:1999;3750-3756.
26. Lajtha L.G., Pozzi L.V., Schofield R., Fox M. Kinetic properties of hematopoietic stem cells. Cell Tissue Kinet. 2:1969;39-44.
27. Cheng T., Rodrigues N., Shen H.et al. Hematopoietic stem cell quiescence maintained by p21cip1/waf1. Science. 287:2000;1804-1808.
28. Mahmud N., Devine S.M., Weller K.P.et al. The relative quiescence of hematopoietic stem cells in nonhuman primates. Blood. 97:2001;3061-3068.
29. Lemischka I.R., Raulet D.H., Mulligan R.C. Developmental potential and dynamic behavior of hematopoietic stem cells. Cell. 45:1986;917-927.
30. Brummendorf T.H., Dragowska W., Zijlmans J.M.J.M., Thornbury G., Lansdorp P.M. Asymmetric cell divisions sustain long-term hematopoiesis from single-sorted human fetal liver cells. J Exp Med. 188:1998;1117-1124.
31. Bryder D., Jacobsen S.E. Interleukin-3 supports expansion of long-term multilineage repopulating activity after multiple stem cell divisions in vitro. Blood. 96:2000;1748-1755.
32. Morrison S.J., Shah N.M., Anderson D.J. Regulatory mechanisms in stem cell biology. Cell. 88:1998;287-298.
33. Lansdorp P.M. Self-renewal of stem cells. Biol Blood Marrow Transplant. 3:1997;171-178.
34. Suda T., Suda J., Ogawa M. Disparate differentiation in mouse hemopoietic colonies derived from paired progenitors. Proc Natl Acad Sci U S A. 81:1984;2520-2524.
35. Mayani H., Dragowska W., Lansdorp P.M. Lineage commitment in human hemopoiesis involves asymmetric cell division of multipotent progenitors and does not appear to be influenced by cytokines. J. Cell Physiol. 157:1993;579.
36. Han W., Ye Q., Moore M.A. A soluble form of human Δ-like-1 inhibits differentiation of hematopoietic progenitor cells. Blood. 95:2000;1616-1625.
37. Punzel M., Gupta P., Verfaillie C.M. The microenvironment of AFT024 cells maintains primitive human hematopoiesis by counteracting contact mediated inhibition of proliferation. Cell Communication and Adhesion. 9:2002;149-159.
38. Hurley R.W., McCarthy J.B., Verfaillie C.M. Direct adhesion to bone marrow stroma via fibronectin receptors inhibits hematopoietic progenitor proliferation. J Clin Invest. 96:1995;5111-5119.
39. Verfaillie C.M. Direct contact between human primitive hematopoietic progenitors and bone marrow stroma is not required for long-term in vitro hematopoiesis. Blood. 79:1992;2821-2826.
40. Bhatia R., Williams A.D., Munthe H.A. Contact with fibronectin enhances preservation of normal but not chronic myelogenous leukemia primitive hematopoietic progenitors. Exp Hematol. 30:2002;324-332.
41. Bhatia R., McCarthy J.B., Verfaillie C.M. Interferon-α restores normal β1 integrin-mediated inhibition of hematopoietic progenitor proliferation by the marrow microenvironment in chronic myelogenous leukemia. Blood. 87:1996;3883-3891.
42. Jiang Y., Prosper F., Verfaillie C.M. Opposing effects of engagement of integrins and stimulation of cytokine receptors on cell cycle progression of normal human hematopoietic progenitors. Blood. 95:2000;846-854.
43. Dao M.A., Hashino K., Kato I., Nolta J.A. Adhesion to fibronectin maintains regenerative capacity during ex vivo culture and transduction of human hematopoietic stem and progenitor cells. Blood. 92:1998;4612-4621.
44. Schofield K.P., Humphries M.J., de Wynter E., Testa N., Gallagher J.T. The effect of α4 β1-integrin binding sequences of fibronectin on growth of cells from human hematopoietic progenitors. Blood. 91:1998;3230-3238.
45. Yokota T., Oritani K., Mitsui H.et al. Growth-supporting activities of fibronectin on hematopoietic stem/progenitor cells in vitro and in vivo. structural requirement for fibronectin activities of CS1 and cell-binding domains Blood. 91:1998;3263-3272.
46. Kapur R., Cooper R., Zhang L., Williams D.A. Cross-talk between α4β1/α5β1 and c-kit results in opposing effect on growth and survival of hematopoietic cells via the activation of focal adhesion kinase, mitogen-activated protein kinase, and Akt signaling pathways. Blood. 97:2001;1975-1981.
47. Kiger A.A., White-Cooper H., Fuller M.T. Somatic support cells restrict germline stem cell self-renewal and promote differentiation. Nature. 407:2000;750-754.
48. Gupta P., Oegema T.R. Jr., Brazil J.J., Dudek A.Z., Slungaard A., Verfaillie C.M. Human LTC-IC can be maintained for at least 5 weeks in vitro when interleukin-3 and a single chemokine are combined with o-sulfated heparan sulfates. requirement for optimal binding interactions of heparan sulfate with early-acting cytokines and matrix proteins Blood. 95:2000;147-155.
49. 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. 294:2001;2542-2545.
50. Tulina N., Matunis E. Control of stem cell self-renewal in Drosophila spermatogenesis by JAK-STAT signaling. Science. 294:2001;2546-2549.