Hierarchical differentiation of multipotent progenitor cells

BioEssays

Volumn 21, Issue 4, 1999, Pages 333-338

  Flickinger, Reed A ^a,b  

^a UNIVERSITY AT BUFFALO   (United States)

^b NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALIA;

EID: 0033119555     PISSN: 02659247     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-1878(199904)21:4<333::AID-BIES10>3.0.CO;2-X     Document Type: Article

References (67)

1. Grigoriadis AE, Heersche JN, Aubin JE. Continuously growing bipotential and monopotential myogenic, adipogenic, and chondrogenic subclones isolated from the monopotential RCJ 3.1 clonal cell line. Dev Biol 1990;142: 313-318.
2. Yamaguchi A, Kahn AJ. Clonal osteogenic cell lines express myogenic and adipogenic developmental potential. Calcif Tissue Int 1991;49:221-225.
3. Yamaguchi A, Katagiri T, Ikeda T, Wozney JM, Rosen V, Wang EA, Kahn AJ, Suda T, Yoshika S. Recombinant human bone morphogenetic protein-2 stimulates osteoblastic maturation and inhibits myogenic differentiation in vitro. J Cell Biol 1991;113:681-687.
4. Yamaguchi A. Regulation of differentiation pathway of skeletal mesenchyme cells in cell lines by transforming growth factor-β superfamily. Semin Cell Biol 1995;6:165-173.
5. Katagiri T, Akiyama S, Namiki M, Komaki M, Yamaguchi A, Rosen V, Wozney JM, Fujisawa-Sehara A, Suda T. Bone morphogenetic protein-2 inhibits terminal differentiation of myogenic cells by suppressing the transcriptional activity of MyoD and myogenin. Exp Cell Res 1997;230:342-351.
6. Marie J. Effects of bone morphogenetic proteins on cells of the osteoblastic lineage. Cell Eng 1997;2:92-99.
7. Shah NM, Marchionni MA, Isaacs I, Stroobant PW, Anderson DJ. Glial growth factor restricts mammalian neural crest stem cells to a glial fate. Cell 1994;77:349-360.
8. Anderson DJ. A molecular switch for the neuron-glia developmental decision. Neuron 1995;15:1219-1222.
9. Jones BW, Fetter RD, Tear G, Goodman CS. Glial cells missing: a genetic switch that controls glial versus neuronal fate. Cell 1995;82:1013-1023.
10. Temple S, Raff MC. Differentiation of a bipotential glial progenitor cell in single cell microculture. Nature 1985;313:223-225.
11. Lillien LE, Raff MC. Differentiation signals in the CNS: type-2 astrocyte development in vitro as a model system. Neuron 1990;5:111-119.
12. Turner DL, Cepko CL. A common progenitor for neurons and glia persists in rat retina late in development. Nature 1987;328:131-136.
13. Cepko CL, Austin CP, Young X, Alexiades M, Ezzeddine D. Cell fate determination in the vertebrate retina. Proc Natl Acad Sci USA 1996;93: 589-595.
14. Mayani H, Dragowska W, Landsdorp PM. Lineage commitment in human hemopoiesis involves asymmetric cell division of multipotent progenitors and does not appear to be influenced by cytokines. J Cell Physiol 1993;157:579-586.
15. Hu M, Krause D, Greaves M, Sharkis S, Dexter M, Heyworth C, Enver T. Multilineage gene expression precedes commitment in the hemopoietic system. Genes Dev 1997;11:774-785.
16. Shah NM, Groves AK, Anderson DJ. Alternative neural crest cell fates are instructively promoted by TGF-β superfamily members. Cell 1996;85:331-343.
17. Anderson DJ. Cellular and molecular biology of neural crest cell lineage determination. Trends Genet 1997;13:276-280.
18. Anderson DJ, Carnahan J, Michelsohn A, Patterson PH. Antibody markers identify a common progenitor to sympathetic neurons and chromaffin cells in vivo, and reveal the timing of commitment to neuronal differentiation in the sympathoadrenal lineage. J Neurosci 1991;11:3507-3519.
19. Doupe AJ, Patterson PH, Landis SC. Small intensely fluorescent cells in culture: Role of glucocorticoids and growth factors in their development and interconversions with other neural crest derivitives. J Neurosci 1985;5:2143-2160.
20. Anderson DJ, Axel R. A bipotential neuroendocrine precursor whose choice of cell fate is determined by NGF and glucocorticoids. Cell 1986;47:1079-1090.
21. Lennon VA, Peterson S, Schubert D. Neuroectoderm markers retained in phenotypical skeletal muscle cells arising from a glial cell line. Nature 1979;281:586-588.
22. Valtz NLM, Hayes TE, Norregaard T, Liu S, McKay RDG. An embryonic origin for medulloblastoma. New Biol 1991;3:364-371.
23. McBurney NM, Jones-Villeneuve EMV, Edwards MKS, Anderson PJ. Control of muscle and neuronal differentiation in a cultured embryonal carcinoma cell line. Nature 1982;299:165-167.
24. Tajbakhsh S, Vivarelli E, Angelis G, Rocancourt D, Buckingham M, Cossu G. A population of myogenic cells derived from the mouse neural tube. Neuron 1994;13:813-821.
25. Tajbakhsh S, Buckingham ME. Lineage restriction of the myogenic conversion factor myf-5 in the brain. Development 1995;121:4077-4083.
26. Hemmati-Brivanlou A, Melton DA. Vertebrate embryonic cells will become nerve cells unless told otherwise. Cell 1997;88:13-17.
27. Ogawa M. Differentiation and proliferation of hematopoietic stem cells. Blood 1993;81:2844-2853.
28. Young JA. The life of vertebrates. 3rd ed. London: Oxford University Press; 1981.
29. Pearse V, Pearse J, Buchsbaum M, Buchsbaum R. Living invertebrates, Palo Alto, CA: Blackwell Scientific; 1987.
30. Weslch U, Storch V. Comparative animal cytology and histology. Seattle, WA: University of Washington Press; 1976.
31. Altschuler DM, Turner DL, Cepko CL. Specification of cell type in the vertebrate retina. In: Lam DMK, Schatz CJ, editors. Development of the visual system. Cambridge: MIT Press; 1991. p 37-58.
32. Bloom GE, Ostlund E, von Euler US, Lishjko F, Titzen M, Adams-Ray J. Studies on catecholamine-containing granules of specific cells in cyclostome hearts. Acta Physiol Scand 1961;53(suppl. 85):1-34.
33. Miller DA, Ratcliffe NA. The evolution of blood cells: facts and enigmas. Endeavour 1989;13:72-77.
34. Grigoriadis AE, Heersche JNM, Aubin JE. Differentiation of muscle, fat, cartilage and bone from progenitor cells present in a bone-derived clonal cell population: effect of dexamethasone. J Cell Biol 1988;106:2139-2151.
35. Williams BP, Abney ER, Raff MC. Macroglial cell development in embryonic rat brain: studies using monoclonal antibodies, fluorescence activated cell sorting and cell culture. Dev Biol 1985;112:126-134.
36. Keller G, Kennedy M, Papayannopoulou T, Wiles MV. Hematopoietic commitment during embryonic stem cell differentiation in culture. Mol Cell Biol 1993;13:473-486.
37. Ito K, Sieber-Blum M. Pluripotent and developmentally restricted neural-crest-derived cells in posterior visceral arches. Dev Biol 1993;156:191-200.
38. Lo L, Johnson JE, Wuenschell CW, Saito T, Anderson DJ. Mammalian achaete-scute homolog I is transiently expressed by spatially-restricted subsets of early neuroepithelial and neural crest cells. Genes Dev 1991;5:1524-1537.
39. Freese E, Yoshida A. The role of mutations in evolution. In: Bryson V, Vogel HJ, editors. Evolving genes and proteins. New York: Academic Press; 1965. p 341-355.
40. Boulikas T. Evolutionary consequences of nonrandom damage and repair of chromatin domains. J Mol Evol 1992;35:156-180.
41. Modrich P. DNA mismatch correction. Annu Rev Biochem 1987;56:435-466.
42. Mielke C, Maass K, Tummler M, Bode J. Anatomy of highly expressing sites targeted by retroviral vectors. Biochemistry 1996;35:2239-2252.
43. Mielke C, Kohwi Y, Kohwi-Shigematsu T, Bode J. Hierarchical binding of DNA fragments derived from scaffold-attached regions: correlation of properties in vitro and function in vivo. Biochemistry 1990;29:7475-7485.
44. Bouvet P, Dimitrov S, Wolffe A. Specific regulation of Xenopus chromosomal 5S rRNA gene transcription in vivo by histone H1. Genes Dev 1994;8:1147-1159.
45. Tomaszewski R, Jerzmanowski A. The AT-rich flanks of the oocyte-type 5S RNA gene of Xenopus laevis act as a strong local signal for histone H1-mediated chromatin reorganization in vitro. Nucleic Acids Res 1997;25: 458-465.
46. Strasbaugh LD, Williams SM. High density of an SAR-associated motif differentiates heterochromatin from euchromatin. J Theor Biol 1996;183: 159-167.
47. Flickinger RA. Cell differentiation: an evolutionary perspective. Int Rev Cytol 1994;148:81-118.
48. Renz M, Day LA. Transition from non-cooperative to cooperative and selective binding of histone H1 to DNA. Biochemistry 1976;15:3220-3228.
49. Izaurralde E, Käs E, Laemmli UK. Highly preferential nucleation of histone H1 assembly on scaffod-associated regions. J Mol Biol 1989;210:573-585.
50. Rupp RAW, Weintraub H. Ubiquitous MyoD transcription at the midblastula transition prededes induction-dependent MyoD expression in presumptive mesoderm of X. laevis. Cell 1991;65:927-937.
51. Dimitrov S, Almouzni G, Dasso M, Wolffe AP. Chromatin transitions during early Xenopus embryogenesis: changes in histone H4 acetylation and in linker histone type. Dev Biol 1993;160:214-227.
52. Steinbach OC, Wolffe A, Rupp RAW. Somatic linker histones cause loss of mesodermal competence in Xenopus. Nature 1997;389:395-399.
53. Rosseau D, Khochbin S, Gorka C, Lawrence JJ. Regulation of histone H1° accumulation during induced differentiation of murine erythroleukemia cells. J Mol Biol 1991;217:85-92.
54. Reeves R, Nissen MS. The A-T-DNA-binding domain of mammalian high mobility group 1 chromosomal proteins. A novel peptide motif recognizing DNA structure. J Biol Chem 1990;265:8573-6582.
55. Wisniewski JR, Grossbach U. Structural and functional properties of linker histones and high mobility group proteins in polytene chromosomes. Int J Dev Biol 1996;40:177-187.
56. Zhao K, Käs E, Gonzales E, Laemmli UK. SAR-dependent mobilization of histone H1 by HMG-1/Y in vitro: HMG1/Y is enriched in H1-depleted chromatin. EMBO J 1993;12:3237-3247.
57. Ura K, Nightingale K, Wolffe AP. Differential association of HMG1 and linker histones B4 and H1 with dinucleosomal DNA: structural transitions and transcriptional repression. EMBO J 1996;15:4959-4969.
58. Seyedin SM, Pehrson JR, Cole RD. Loss of chromosomal high mobility group proteins HMG 1 and HMG 2 when mouse neuroblastoma and Friend erythroleukemia cells become committed to differentiation. Proc Natl Acad Sci USA 1981;78:5988-5992.
59. Heads RJ, Carpenter BG. Differential synthesis of histone H1 during early spherulation in Physarum polycephalum. Biochim Biophys Acta 1990;1053: 56-62.
60. Weintraub H. The MyoD family and myogenesis, networks and thresholds. Cell 1993;75:1241-1244.
61. Cross MA, Heyworth CM, Murrell AM, Bockman EO, Dexter TM, Green AR. Expression of lineage restricted transcription factors precedes lineage specific differentiation in a multipotent hemopoietic progenitor cell line. Oncogene 1994;9:3013-3016.
62. Moreau J, Scherrer K. Co-evolution of base composition and codon useage in Xenopus laevis and human globin genes with long-range DNA organization of the genome. FEBS Lett 1987;221:3-10.
63. +) nuclear RNA of frog embryo and Friend erythroleukemia cells. Dev Growth Diff 1987;30:9-14.
64. Affara N, Daubas P. Regulation of a group of abundant mRNA sequences during Friend cell differentiation. Dev Biol 1979;72:110-125.
65. Larson DE, Xie W, Glibetic M, OMahony D, Sells BH, Rothblum LI. Coordinated decreases in rRNA gene transcription factors and rRNA synthesis during muscle cell differentiation. Proc Natl Acad Sci USA 1993;90:7933-7936.
66. Maheshwari Y, Rao M, Sykes DE, Tyner AL, Weiser MM. Changes in ribosomal protein and ribosomal RNA synthesis during rat intestinal differentiation. Cell Growth Diff 1993;4:745-752.
67. Sherton CE, Kabat D. Changes in RNA and protein metabolism preceding onset of hemoglobin synthesis in cultured Friend leukemia cells. Dev Biol 1976;48:118-131.