Concise reviews: A stem cell apostasy: A tale of four H words

Stem Cells

Volumn 33, Issue 1, 2015, Pages 15-20

  Quesenberry, Peter J ^a   Goldberg, Laura R ^a   Dooner, Mark S ^a  

^a RHODE ISLAND HOSPITAL   (United States)

Author keywords

Colony forming units; Extracellular vesicles; Hematopoietic progenitor cells; Hematopoietic stem cells; Microenvironment; Tissue stem cells

Indexed keywords

CELL SURFACE MARKER; EPITOPE;

BONE MARROW; CELL DIFFERENTIATION; CELL ISOLATION; CYTOLOGY; GENE EXPRESSION; HEMATOPOIESIS; HEMATOPOIETIC STEM CELL; HUMAN; NONHUMAN; PHENOTYPE; REVIEW; SELF CONCEPT; STEM CELL TRANSPLANTATION; ANIMAL; METABOLISM; PHYSIOLOGY; STEM CELL;

ANIMALS; CELL DIFFERENTIATION; HEMATOPOIETIC STEM CELLS; HUMANS; STEM CELLS;

EID: 84919459989     PISSN: 10665099     EISSN: 15494918     Source Type: Journal    
DOI: 10.1002/stem.1829     Document Type: Review

References (64)

1. Till JE, McCulloch EA,. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiat Res 1961; 14: 213-222.
2. Till JE, McCulloch EA, Siminovitch L,. A stochastic model of stem cell proliferation, based on the growth of spleen colony-forming cells. Proc Natl Acad Sci USA 1964; 51: 29-36.
3. Bradley TR, Metcalf D,. The growth of mouse bone marrow cells in vitro. Aust J Exp Biol Med Sci 1966; 44: 287-299.
4. Pluznik DH, Sachs L,. The cloning of normal "mast" cells in tissue culture. J Cell Physiol 1965; 66: 319-324.
5. Axelrad AA, McLeod DL, Suzuki S, et al. Regulation of the population size of erythropoietic progenitor cells. In:, Clarkson B, Marks PA, Till JE, eds. Differentiation of Normal and Neoplastic Hematopoietic Cells. New York, Cold Sring Harbor, 1978: 155.
6. Metcalf D, MacDonald HR, Odartchenko N, et al. Growth of mouse megakaryocyte colonies in vitro. Proc Natl Acad Sci USA 1975; 72: 1744-1748.
7. Nakeff A, Dicke KA, Van Noord MJ,. Megakaryocytes in agar culture of mouse bone marrow. Ser Haematol 1975; 8: 4-21.
8. Gregory CJ,. Erythropoietin sensitivity as a differentiation marker in the hemopoietic system: Studies of three erythropoietic colony responses in culture. J Cell Physiol 1976; 89: 289-301.
9. Long MW, Gragowski LL, Heffner CH, et al. Phorbol diesters stimulate the development of an early murine progenitor cell. The burst-forming unit-megakaryocyte. J Clin Invest 1985; 76: 431-438.
10. Bradley TR, Hodgson GS,. Detection of primitive macrophage progenitor cells in mouse bone marrow. Blood 1979; 54: 1446-1450.
11. Suda T, Suda J, Ogawa M,. Single cell origin of mouse hemopoietic colonies expressing multiple lineages in variable combinations. Proc Natl Acad Sci USA 1983; 80: 6689-6693.
12. Spangrude GJ, Heimfeld S, Weissman IL,. Purification and characterization of mouse hematopoietic stem cells. Science 1988; 241: 58-62.
13. Forsberg EC, Prohaska SS, Katzman S, et al. Differential expression of novel potential regulators in hematopoietic stem cells. PLoS Genet 2005; 1: e28.
14. Rossi DJ, Bryder D, Zahn JM, et al. Cell intrinsic alterations underlie hematopoietic stem cell aging. Proc Natl Acad Sci USA 2005; 102: 9194-9199.
15. Arber C, BitMansour A, Sparer TE, et al. Common lymphoid progenitors rapidly engraft and protect against lethal murine cytomegalovirus infection after hematopoietic stem cell transplantation. Blood 2003; 102: 421-428.
16. Manz MG, Miyamoto T, Akashi K, et al. Prospective isolation of human clonogenic common myeloid progenitors. Proc Natl Acad Sci USA 2002; 99: 11872-11877.
17. Miyamoto T, Iwasaki H, Reizis B, et al. Myeloid or lymphoid promiscuity as a critical step in hematopoietic lineage commitment. Dev Cell 2002; 3: 137-147.
18. Christensen JL, Weissman IL,. Flk-2 is a marker in hematopoietic stem cell differentiation: A simple method to isolate long-term stem cells. Proc Natl Acad Sci USA 2001; 98: 14541-14546.
19. Kondo M, Scherer DC, King AG, et al. Lymphocyte development from hematopoietic stem cells. Curr Opin Genet Dev 2001; 11: 520-526.
20. Kondo M, Scherer DC, Miyamoto T, et al. Cell fate conversion of lymphoid-committed progenitors by instructive actions of cytokines. Nature 2000; 407: 383-386.
21. Akashi K, Traver D, Miyamoto T, et al. A clonogenic common myeloid progenitor that gives rise to all myeloid lineages. Nature 2000; 404: 193-197.
22. Cheshier SH, Morrison SJ, Liao X, et al. In vivo proliferation and cell cycle kinetics of long-term self-renewing hematopoietic stem cells. Proc Natl Acad Sci USA 1999; 96: 3120-3125.
23. Kondo M, Weissman IL, Akashi K,. Identification of clonogenic common lymphoid progenitors in mouse bone marrow. Cell 1997; 91: 661-672.
24. Morrison SJ, Wandycz AM, Hemmati HD, et al. Identification of lineage of multipotent hematopoietic progenitors. Development 1997; 124: 1929-1939.
25. Adolfsson J, Mansson R, Buza-Vidas N, et al. Identification of Flt3+ lympho-myeloid stem cells lacking erythro-megakaryocytic potential: A revised road map for adult blood lineage commitment. Cell 2005; 121: 295-306.
26. Randal TD, Lund FE, Howard MD, et al. Expression of murine CD38 defines a population of long-term reconstituting hematopoietic stem cells. Blood 1996; 87: 4057-4067.
27. Morrison SJ, Weissman IL,. The long-term repopulating subset of hematopoietic stem cells is deterministic and isolatable by phenotype. Immunity 1994; 1: 661-673.
28. Forsberg EC, Bhattacharya D, Weissman IL,. Hematopoietic stem cells: Expression profiling and beyond. Stem Cell Rev 2006; 2: 23-30. Review.
29. Warren L, Bryder D, Weissman IL, et al. Transcription factor profiling in individual hematopoietic progenitors by digital RT-PCR. Proc Natl Acad Sci USA 2006; 103: 17807-17812.
30. Bryder D, Rossi DJ, Weissman IL,. Hematopoietic stem cells: The paradigmatic tissue-specific stem cell. Am J Pathol 2006; 169: 338-346, Erratum in: Am J Pathol 169:1899.
31. Forsberg EC, Serwold T, Kogan S, et al. New evidence supporting megakaryocyte-erythrocyte potential of flk2/flt3+ multipotent hematopoietic progenitors. Cell 2006; 126: 415-426.
32. Suda T, Suda J, Ogawa M,. Disparate differentiation in mouse hemopoietic colonies derived from paired progenitors. Proc Natl Acad Sci USA 1984; 81: 2520-2524.
33. Passegue E, Wagers AJ, Giuriato S, et al. Global analysis of proliferation and cell cycle gene expression in the regulation of hematopoietic stem and progenitor cell fates. J Exp Med 2005; 202: 1599-1611.
34. Fleming WH, Alpern EJ, Uchida N, et al. Functional heterogeneity is associated with the cell cycle status of murine hematopoietic stem cells. J Cell Biol 1993; 122: 897-902.
35. Orschell-Traycoff CM, Hiatt K, Dagher RN, et al. Homing and engraftment potential of Sca-1+lin- cells fractionated on the basis of adhesion molecule expression and position in cell cycle. Blood 2000; 96: 1380-1387.
36. Quesenberry PJ,. The blueness of stem cells. Exp Hematol 1991; 19: 725-728.
37. Suda J, Suda J, Ogawa M,. Analysis of differentiation of mouse hemopoietic stem cells in cultures by sequential replating of paired progenitors. Blood 1984; 64: 393-399.
38. Nilsson SK, Dooner MS, Tiarks CY, et al. Potential and distribution of transplanted hematopoietic stem cells in a non-ablated mouse model. Blood 1997; 89: 4013-4020.
39. Yimez OH, Kiel MJ, Morrison SJ,. Slam family markers are conserved among hematopoietic stem cells from old and reconstituted mice and markedly increase their purity. Blood 2006; 107: 924-930.
40. Peters SO, Kittler EL, Ramshaw HS, et al. Murine marrow cells expanded in culture with IL-3, IL-6, IL-11, and SCF acquire an engraftment defect in normal hosts. Exp Hematol 1995; 23: 461-469.
41. Peters SO, Kittler EL, Ramshaw HS, et al. Ex vivo expansion of murine marrow cells with interleukin-3 (IL-3), IL-6, IL-11, and stem cell factor leads to impaired engraftment in irradiated hosts. Blood 1996; 87: 30-37.
42. Habibian HK, Peters SO, Hsieh CC, et al. The fluctuating phenotype of the lympho-hematopoietic stem cell with cell cycle transit. J Exp Med 1998; 188: 393-398.
43. Colvin GA, Dooner MS, Dooner GJ, et al. Stem cell continuum: Directed differentiation hotspots. Exp Hematol 2007; 35: 96-107.
44. Cerny J, Dooner M, McAuliffe C, et al. Homing of purified murine lymphohematopoietic stem cells: A cytokine-induced defect. J Hematother. Stem Cell Res 2002; 11: 913-922.
45. Becker PS, Nilsson SK, Li Z, et al. Adhesion receptor expression by hematopoietic cell lines and murine progenitors: Modulation by cytokines and cell cycle status. Exp Hematol 1999; 27: 533-541.
46. Berrios VM, Dooner GJ, Nowakowski G, et al. The molecular basis for the cytokine-induced defect in homing and engraftment of hematopoietic stem cells. Exp Hematol 2001; 29: 1326-1335.
47. Lambert JF, Liu M, Colvin GA, et al. Marrow stem cells shift gene expression and engraftment phenotype with cell cycle transit. J Exp Med 2003; 197: 1563-1572.
48. Colvin GA, Lambert JF, Moore BE, et al. Intrinsic hematopoietic stem cell/progenitor plasticity: Inversions. J Cell Physiol 2004; 199: 20-31.
49. Reddy GP, McAuliffe CI, Pang L, et al. Cytokine receptor repertoire and cytokine responsiveness of Ho dull/Rh dull stem cells with differing potentials for G1/S phase progression. Exp Hematol 2002; 30: 792-800.
50. Aliotta JM, Lee D, Puente N, et al. Progenitor/stem cell fate determination: Interactive dynamics of cell cycle and microvesicles. Stem Cells Dev 2012; 21: 1627-1638.
51. Goldberg LR, Dooner MS, Johnson K, et al. The murine long-term multi-lineage renewal marrow stem cell is a cycling cell. Leukemia 2014; 28: 813-822.
52. Kiel MJ, Yilmaz OH, Iwashita T, et al. SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells. Cell 2005; 121: 1109-1121.
53. Hock H,. Some hematopoietic stem cells are more equal than others. J Exp Med 2010; 207: 1127-1130.
54. Copley MR, Beer PA, Eaves CJ,. Hematopoietic stem cell heterogeneity takes center stage. Cell Stem Cell 2012; 10: 690-697.
55. Morita Y, Ema H, Nakauchi H,. Heterogeneity and hierarchy within the most primitive hematopoietic stem cell compartment. J Exp Med 2010; 207: 1173-1182.
56. Oguro H, Ding L, Morrison S,. SLAM family markers resolve functionally distinct subpopulations of hematopoietic stem cells and multipotent progenitors. Cell Stem Cell 2013; 13: 102-116.
57. Ogawa M,. Changing phenotypes of hematopoietic stem cells. Exp Hematol 2002; 30: 3-6.
58. Goodell MA, Brose K, Paradis G, et al. Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo. J Exp Med 1996; 183: 1797-1806.
59. Keller S, Sanderson MP, Stoeck A, et al. Exosomes: From biogenesis and secretion to biological function. Immunol Lett 2006; 107: 102-108.
60. Heijnen HF, Schiel AE, Fijnheer R, et al. Activated platelets release two types of membrane vesicles: Microvesicles by surface shedding and exosome derived from exocytosis of multivesicular bodies and alpha granules. Blood 1999; 94: 3791-3799.
61. Thery C, Ostrowski M, Segura E,. Membrane vesicles as conveyors of immune responses. Nat Rev Immunol 2009; 9: 581-593.
62. Aliotta JM, Sanchez-Guijo FM, Dooner GJ, et al. Alteration of marrow gene expression, protein production, and engraftment into lung by lung-derived microvesicles: A novel mechanism for phenotype modulation. Stem Cells 2007; 25: 2245-2256.
63. Aliotta JM, Pereira M, Johnson KW, et al. Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription. Exp Hematol 2010; 38: 233-245.
64. Aliotta JM, Pereira M, Li M, et al. Stable cell fate changes in marrow cells induced by lung-derived microvesicles. J Extracell Vesicles 2012; 1.