Phylogeny and Ontogeny of the Hematopoietic Microenvironment

References

• Miyake, K., Weissman, I. L., Greenberger, J. S. and Kincade, P. W. (1991). Evidence for a role of the integrin VLA-4 in lympho-hemopoiesis. J Exp Med, 173(3), 599–607.
   PubMed Web of Science ®Google Scholar
• Simmons, P. J., Zannettino, A., Gronthos, S. and Leavesley, D. (1994). Potential adhesion mechanisms for localisation of haemopoietic progenitors to bone marrow stroma. [Review] Leuk Lymphoma, 12(5–6), 353–63.
   PubMed Web of Science ®Google Scholar
• Zannettino, A. C., Berndt, M. C., Butcher, C., Butcher, E. C., Vadas, M. A. and Simmons, P. J. (1995). Primitive human hematopoietic progenitors adhere to P-selectin (CD62P). Blood, 85(12), 3466–77.
   PubMed Web of Science ®Google Scholar
• Baumheter, S., Singer, M. S., Henzel, W., Hemmerich, S., Renz, M., Rosen, S. D. and Lasky, L. A. (1993). Binding of L-selectin to the vascular sialomucin CD34. Science, 262, 436–8.
   PubMed Web of Science ®Google Scholar
• Lasky, L. A. (1992). Selectins: interpreters of cell-specific carbohydrate information during inflammation. [Review] Science, 258(5084), 964–9.
   Web of Science ®Google Scholar
• Ikuta, K., Kina, T., MacNeil, I., Uchida, N., Peault, B., Chien Yueh-hsiu and Weissman, I. L. (1990). A developmental switch in thymic lymphocyte maturation potential occurs at the level of hematopoietic stem cells. Cell, 62, 863–874.
   PubMed Web of Science ®Google Scholar
• Spangrude, G. J., Heimfeld, S. and Weissman, I. L. (1988). Purification and characterization of mouse hematopoietic stem cells. Science, 241, 58–62.
   PubMed Web of Science ®Google Scholar
• Till, J. E. and McCulloch, E. A. (1961). A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiat Res, 14, 213–222.
   PubMed Web of Science ®Google Scholar
• Becker, A. J., McCulloch, E. A. and Till, J. E. (1963). Cytological demonstration of the clonal nature of spleen colonies derived from transplanted marrow cells. Nature, 197, 452–454.
   PubMed Web of Science ®Google Scholar
• Siminovitch, L., McCulloch, E. A. and Till, J. E. (1963). The distribution of colony-forming cells among spleen colonies. J Cellular Comp Physiol, 62, 327–336.
   PubMedGoogle Scholar
• Wu, A. M., Till, J. E., Siminovitch, L. and McCulloch, E. A. (1968). cytological evidence for a relationship between normal hematopoietic colony-forming cells and cells of the lymphoid system. J Exp Med, 127, 455–464.
   PubMed Web of Science ®Google Scholar
• Till, J. E., McCulloch, E. A. and Siminovitch, L. (1964). A stochastic model of stem cell proliferation, based on the growth of spleen colony-forming cells. Proc Natl Acad Sci, USA, 51, 29.
   Google Scholar
• Mayani, H. and Lansdorp, P. M. (1995). Proliferation of individual hematopoietic progenitors purified from umbilical cord blood. Exp Hematol, 23(14), 1453–62.
   PubMed Web of Science ®Google Scholar
• Mayani, H., Dragowska, W. and Lansdorp, P. M. (1993). Lineage commitment in human hemopoiesis involvesv asymmetric cell division of multipotent progenitors and does not appear to be influenced by cytokines. J Cell Physiol, 157(3), 579–86.
   PubMed Web of Science ®Google Scholar
• Mayani, H., Guilbert, L. J. and Janowska-Wieczorek, A. (1992). Biology of the hemopoietic microenvironment. [Review] Eur J Haematol, 49(5), 225–33.
   PubMed Web of Science ®Google Scholar
• Abkowitz, J. L., Catlin, S. N. and Guttorp, P. Evidence that hematopoiesis may be a stochastic process in vivo.
   Google Scholar
• Abkowitz, J. L., Persik, M. T., Shelton, G. H., Ott, R. L., Kiklevich, J. V., Catlin, S. N. and Guttorp, P. (1995). Behavior of hematopoietic stem cells in a large animal. Proc Natl Acad Sci USA, 92(6), 2031–5.
   PubMed Web of Science ®Google Scholar
• Wolf, N. S. and Trentin, J. J. (1968). Ematopoietic colony studies V.: Effect of hematopoietic organ stroma on differentiation of pluripotent stem cells. J Exp Med, 127, 205.
   PubMed Web of Science ®Google Scholar
• Wolf, N. S. (1979). The hematopoietic microenvironment. Clin Haematol, 8, 469.
   PubMedGoogle Scholar
• Trentin, J. J. (1970). Influence of hematopoietic organ stroma (hematopoietic inductive microenvironments) on stem cell differentiation, Regulation of Hematopoiesis. Vol 1 Edited by AS gordon. New York, Appleton-Centroy-Crofts, pp. 161–186.
   Google Scholar
• Trentin, J. J., Curry, J. L., Wolf, N. and Cheng, V. (1968). Factors controlling stem cell differentiation and proliferation: the hematopoietic inductive microenvironment (HIM), The Proliferation and Spread of Neoplastic Cells. Baltimore, The Williams and Wilkins Co, pp. 713–731.
   Google Scholar
• Trentin, J. J., McGarry, M. P., Jenkins, V. K., Gallagher, M. T., Speirs, R. S. and Wolf, N. S. (1971). Role of inductive microenvironments on hematopoietic (and lymphoid?) differentiation, and role of thymic cells in the eosinophilic granulocyte response to antigen, Morphological and Functional Aspects of Immunity. Edited by K. Lindahl_kiessling, G. Alm, M. G. Hanna Jr. New York, Plenum Press, pp. 289–298.
   Google Scholar
• Gilbert, S. F. (1994). Developmental Biology, 4th Edition, Sinauer Assoc., Inc, Pub, Sunderland, Mass, USA.
   Google Scholar
• Kirk, D. L. and Harper, J. F. (1986). Genetic, biochemical, and molecular approaches to Volvox development and evolution. [Review] Int Rev Cytol, 99, 217–93.
   PubMedGoogle Scholar
• Kirk, D. L., Kaufman, M. R., Keeling, R. M. and Stamer, K. A. (1991). Genetic and cytological control of the asymmetric divisions that pattern the Volvox embryo. Dev, (1), 67–82.
   Google Scholar
• Kirk, D. L. (1988). The ontogeny and phylogeny of cellular differentiation in Volvox. [Review] Trends Genet, 4(2), 32–6.
   PubMed Web of Science ®Google Scholar
• Kirk, D. L., Birchem, R. and King, N. (1986). The extracellular matrix of Volvox: a comparative study and proposed system of nomenclature. J Cell Sci, 80, 207–31.
   PubMed Web of Science ®Google Scholar
• Greenberger, J. S., Sakakeeny, M. and Parker, L. M. (1979). In vitro proliferation of hemopoietic stemcells in long-term marrow cultures: principles in mouse applied to man. Exp Hematol, 7(5), 135–48.
   PubMedGoogle Scholar
• Greenberger, J. S. (1991). The hematopoietic microenvironment. [Review] Crit Rev Oncol Hematol, 11(1), 65–84.
   PubMed Web of Science ®Google Scholar
• Simmons, P. J., Gronthos, S., Zannettino, A., Ohta, S. and Graves, S. (1994). Isolation, characterization and functional activity of human marrow stromal progenitors in hemopoiesis. Prog Clin Biol Res, 389, 271–80.
   PubMedGoogle Scholar
• Zuckerman, K. S. and Wicha, M. S. (1983). Extracellular matrix production by the adherent cells of long-term murine bone marrow cultures. Blood, 61(3), 540–7.
   PubMed Web of Science ®Google Scholar
• Zuckerman, K. S. (1984). Composition and function of the extracellular matrix in the stroma of long-term bone marrow cell cultures. [Review] Kroc Found Ser, 18, 157–70.
   PubMedGoogle Scholar
• Zuckerman, K. S. and Rhodes, R. K. (1985). The hematopoietic extracellular matrix. Prog Clin Biol Res, 184, 257–66.
   PubMedGoogle Scholar
• Zuckerman, K. S., Rhodes, R. K., Goodrum, D. D., Patel, V. R., Sparks, B., Wells, J., Wicha, M. S. and Mayo, L. A. (1985). Inhibition of collagen deposition in the extracellular matrix prevents the establishment of a stroma supportive of hematopoiesis in long-term murine bone marrow cultures. J Clin Invest, 75(3), 970–5.
   PubMed Web of Science ®Google Scholar
• Deryugina, E. I. and Muller-Sieburg, C. E. (1993). Stromal cells in long-term cultures: keys to the elucidation of hematopoietic development?. [Review] Crit Rev Immunol, 13(2), 115–50.
   PubMed Web of Science ®Google Scholar
• Anklesaria, P., Greenberger, J. S., Fitzgerald, T. J., Sullenbarger, B., Wicha, M. and Campbell, A. (1991). Hemonectin mediates adhesion of engrafted murine progenitors to a clonal bone marrow stromal cell line from SI/SId mice. Blood, 77(8), 1691–8.
   PubMed Web of Science ®Google Scholar
• Linenberger, M. L., Jacobson, F. W., Bennett, L. G., Broudy, V. C., Martin, F. H. and Abkowitz, J. L. (1995). Stem cell factor production by human marrow stromal fibroblasts. Exp Hematol, 23(10), 1104–14.
   PubMed Web of Science ®Google Scholar
• Geissler, E. N. and Russell, E. S. (1983). Analysis of the hematopoietic effects of new dominant spotting (W) mutations of the mouse. I. Influence upon hematopoietic stem cells. Exp Hematol, 11(6), 452–60.
   PubMed Web of Science ®Google Scholar
• Geissler, E. N., McFarland, E. C. and Russell, E. S. (1981). Analysis of pleiotropism at the dominant white-spotting (W) locus of the house mouse: a description of ten new W alleles. Genetics, 97(2), 337–61.
   PubMed Web of Science ®Google Scholar
• Lamoreux, M. L. and Russell, E. S. (1979). Developmental interaction in the pigmentary system of mice. I. Interactions between effects of genes on color of pigment and on distribution of pigmentation in the coat of the house mouse (Mus musculus). J Hered, 70(1), 31–6.
   PubMed Web of Science ®Google Scholar
• Russell, E. S. (1979). Hereditary anemias of the mouse: a review for geneticists. [Review] Adv Genet, 20, 357–459.
   Google Scholar
• Wolf, N. S. (1974). Dissecting the hematopoietic microenvironment. I Stem cell lodgement and committment, and proliferation and differentiation of erythropoietic descendants in the SI/SId mouse. Cell Tissue Kinetics, 7, 89–98.
   PubMedGoogle Scholar
• Russell, E. S., Bernstein, S. E., McFarland, E. C. and Modeen, W. R. (1963). The cellular basis of differential radiosensitivity of normal and genetically anemic mice. Radiat Res, 20, 677–694.
   PubMed Web of Science ®Google Scholar
• McCulloch, E. A., Siminovitch, L., Till, J. E., Russell, E. S. and bernstein, S. E. (1965). The cellular basis of the genetically determined hematopoietic defect in anemic mice or genotype SI/SId. Blood, 26, 399–410.
   PubMed Web of Science ®Google Scholar
• McCulloch, E. A., Siminovitch, L. and Till, J. E. (1964). Spleen-Colony formation in anemic mice of genotype W/Wv. Science, 144, 844–846.
   PubMed Web of Science ®Google Scholar
• Boggs, S. S., Boggs, D. R. and Walter, M. (1978). Differing patterns of erythropoiesis following wholebody irradiation in W/Wv and S1/S1d mice. Rad Res, 74, 334–344.
   Web of Science ®Google Scholar
• Boggs, S. S., Wilson, S. M. and Smith, W. W. (1973). Effects of endotoxin on hematopoiesis in irradiated and non-irradiated W/Wv mice. Rad Res, 56, 481–493.
   PubMed Web of Science ®Google Scholar
• Boggs, D. R., Saxe, D. F. and Boggs, S. S. (1983). Aging and hematopoiesis II. The ability of bone marrow cells from young and aged mice to cure and maintain cure in W/Wv. Transplantation, 37, 300–306.
   Web of Science ®Google Scholar
• Boggs, D. R., Boggs, S. S., Saxe, D. F., Gress, L. A. and Canfield, D. R. (1982). Hematopoietic stem cells with high proliferative potential: Assay of their concentration in marrow by the frequency and duration of cure of W/Wv mice. J Clin Invest, 70, 242–253.
   PubMed Web of Science ®Google Scholar
• Ruscetti, F. W., Boggs, D. R., Torok, B. J. and Boggs, S. S. (1976). Reduced blood and marrow neutrophils and granulocytic colony forming cells in Sl/Sld mice. Proc Soc Exp Biol Med, 152, 398–402.
   PubMed Web of Science ®Google Scholar
• Geissler, E. N., Liao, M., Brook, J. D., Martin, F. H., Zsebo, K. M., Housman, D. E. and Galli, S. J. (1991). Stem cell factor (SCF), a novel hematopoietic growth factor and ligand for c-kit tyrosine kinase receptor, maps on human chromosome 12 between 12q14.3 and 12qter. Somat Cell Mol Genet, 17(2), 207–14.
   PubMedGoogle Scholar
• Zsebo, K. M., Wypych, J., McNiece, I. K., Lu, H. S., Smith, K. A., Karkare, S. B., Sachdev, R. K., Yuschenkoff, V. N., Birkett, N. C., Williams, L. R., et al., (1990). Identification, purification, and biological characterization of hematopoietic stem cell factor from buffalo rat liver—conditioned medium. Cell, 63(1), 195–201.
   PubMed Web of Science ®Google Scholar
• Zsebo, K. M., Williams, D. A., Geissler, E. N., Broudy, V. C., Martin, F. H., Atkins, H. L., Hsu, R. Y., Birkett, N. C., Okino, K. H., Murdock, D. C., et al., (1990). Stem cell factor is encoded at the S1 locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor. Cell, 63(1), 213–24.
   PubMed Web of Science ®Google Scholar
• Nocka, K., Tan, J. C., Chiu, E., Chu, T. Y., Ray, P., Traktman, P. and Besmer, P. (1990). Molecular bases of dominant negative and loss of function mutations at the murine c-kit/white spotting locus: W37, Wv, W41 and W. EMBO J, 9(6), 1805–13.
   PubMed Web of Science ®Google Scholar
• Huang, E., Nocka, K., Beier, D. R., Chu, T. Y., Buck, J., Lahm, H. W., Wellner, D., Leder, P. and Besmer, P. (1990). The hematopoietic growth factor KL is encoded by the S1 locus and is the ligand of the c-kit receptor, the gene product of the W locus. Cell, 63(1), 225–33.
   PubMed Web of Science ®Google Scholar
• Bernstein, A., Chabot, B., Dubreuil, P., Reith, A., Nocka, K., Majumder, S., Ray, P. and Besmer, P. (1990). The mouse W/c-kit locus. [Review] Ciba Found Symp, 148, 158–66; discussion, 166–72.
   PubMedGoogle Scholar
• Migliaccio, G., Migliaccio, A. R., Valinsky, J., Langley, K., Zsebo, K., Visser, J. W. and Adamson, J. W. (1991). Stem cell factor induces proliferation and differentiation of highly enriched murine hematopoietic cells. Proc Natl Acad Sci USA, 88(16), 7420–4.
   PubMed Web of Science ®Google Scholar
• Godin, I., Deed, R., Cooke, J., Zsebo, K., Dexter, M. and Wylie, C. C. (1991). Effects of the steel gene product on mouse primordial germ cells in culture. Nature, 352(6338), 807–9.
   PubMed Web of Science ®Google Scholar
• Nocka, K., Majumder, S., Chabot, B., Ray, P., Cervone, M., Bemstein, A. and Besmer, P. (1989). Expression of c-kit gene products in known cellular targets of W mutations in normal and W mutant mice—evidence for an impaired c-kit kinase in mutant mice. Genes Dev, 3(6), 816–26.
   PubMed Web of Science ®Google Scholar
• Matsui, Y., Zsebo, K. M. and Hogan, B. L. (1990). Embryonic expression of a haematopoietic growth factor encoded by the S1 locus and the ligand for c-kit. Nature, 347(6294), 667–9.
   PubMed Web of Science ®Google Scholar
• Motro, B., van der Kooy, D., Rossant, J., Reith, A. and Bernstein, A. (1991). Contiguous patterns of c-kit and steel expression: analysis of mutations at the W and S1 loci. Development, 113(4), 1207–21.
   PubMed Web of Science ®Google Scholar
• Matsui, Y., Toksoz, D., Nishikawa, S., Nishikawa, S., Williams, D., Zsebo, K. and Hogan, B. L. (1991). Effect of Steel factor and leukaemia inhibitory factor on murine primordial germ cells in culture. Nature, 353(6346), 750–2.
   PubMed Web of Science ®Google Scholar
• Manova, K., Nocka, K., Besmer, P. and Bachvarova, R. F. (1990). Gonadal expression of c-kit encoded at the W locus of the mouse. Development, 110(4), 1057–69.
   PubMed Web of Science ®Google Scholar
• Fleischman, R. A., Simpson, F., Gallardo, T., Jin, X. L. and Perkins, S. (1995). Isolation of endothelial-like stromal cells that express Kit ligand and support in vitro hematopoiesis. Exp Hematol, 23(13), 1407–16.
   PubMed Web of Science ®Google Scholar
• Kirk, M. M., Ransick, A., McRae, S. E. and Kirk, D. L. (1993). The relationship between cell size and cell fate in Volvox carteri. J Cell Biol, 123(1), 191–208.
   PubMed Web of Science ®Google Scholar
• Kirk, D. L. (1994). Germ cell specification in Volvox carteri. [Review] Ciba Found Symp, 182, 2–15; discussion, 15–30.
   PubMedGoogle Scholar
• Tam, L. W., Stamer, K. A. and Kirk, D. L. (1991). Early and late gene expression programs in developing somatic cells of Volvox carteri. Dev Biol, 145(1), 67–76.
   PubMed Web of Science ®Google Scholar
• Tam, L. W. and Kirk, D. L. (1991). Identification of cell-type-specific genes of Volvox carteri and characterization of their expression during the asexual life cycle. Dev Biol, 145(1), 51–66.
   PubMed Web of Science ®Google Scholar
• Larson, A., Kirk, M. M. and Kirk, D. L. (1992). Molecular phylogeny of the volvocine flagellates. Mol Biol Evol, 9(1), 85–105.
   PubMed Web of Science ®Google Scholar
• Schmitt, R., Fabry, S. and Kirk, D. L. (1992). In search of molecular origins of cellular differentiation in Volvox and its relatives. [Review] Int Rev Cytol, 139, 189–265.
   PubMed Web of Science ®Google Scholar
• Horvitz, H. R. and Herskowitz, I. (1992). Mechanisms of asymmetric cell division: two Bs or not two Bs, that is the question. [Review] Cell, 68(2), 237–55.
   Web of Science ®Google Scholar
• Shivdasani, R. A., Mayer, E. L. and Orkin, S. H. (1995). Absence of blood formation in mice lacking the T-cell leukaemia oncoprotein tal-1/SCL. Nature, 373(6513), 432–4.
   PubMed Web of Science ®Google Scholar
• Shivdasani, R. A. and Orkin, S. H. (1995). Erythropoiesis and globin gene expression in mice lacking the transcription factor NF-E2. Proc Natl Acad Sci USA, 92(19), 8690–4.
   PubMed Web of Science ®Google Scholar
• Shivdasani, R. A. and Orkin, S. H. (1996). The transcriptional control of hematopoiesis. [Review] Blood, 87(10), 4025–39.
   PubMed Web of Science ®Google Scholar
• Georgopoulos, K., Bigby, M., Wang, J. H., Molnar, A., Wu, P., Winandy, S. and Sharpe, A. (1994). The Ikaros gene is required for the development of all lymphoid lineages. Cell, 79(1), 143–56.
   PubMed Web of Science ®Google Scholar
• Kelley, C., Yee, K., Harland, R. and Zon, L. I. (1994). Ventral expression of GATA-1 and GATA-2 in the Xenopus embryo defines induction of hematopoietic mesoderm. Dev Biol, 165(1), 193–205.
   PubMed Web of Science ®Google Scholar
• Yee, K., Bishop, T. R., Mather, C. and Zon, L. I. (1993). Isolation of a novel receptor tyrosine kinase cDNA expressed by developing erythroid progenitors. Blood, 82(4), 1335–43.
   PubMed Web of Science ®Google Scholar
• Stainier, D. Y., Weinstein, B. M., Detrich, H. W. 3rd, Zon, L. I. and Fishman, M. C. (1995). Cloche, an early acting zebrafish gene, is required by both the endothelial and hematopoietic lineages. Development, 121(10), 3141–50.
   PubMed Web of Science ®Google Scholar
• Van Zant, G., Scott-Micus, K., Thompson, B. P., Fleischman, R. A. and Perkins, S. (1992). Stem cell quiescence/activation is reversible by serial transplantation and is independent of stromal cell genotype in mouse aggregation chimeras. Exp Hematol, 20(4), 470–5.
   PubMed Web of Science ®Google Scholar
• Sharma, H. W., Maltese, J. Y., Zhu, X., Kaiser, H. E. and Narayanan, R. (1996). Telomeres, telomerase and cancer: is the magic bullet real?. [Review] Anticancer Res, 16(1), 511–5.
   PubMed Web of Science ®Google Scholar
• Sharma, H. W., Sokoloski, J. A., Perez, J. R., Maltese, J. Y., Stein, C. A., Nichols, G., Khaled, Z., Telang, N. T. and Narayanan, R. (1995). Differentiation of immortal cells inhibits telomerase activity. Proc Natl Acad Sci USA, 92(26), 12343–6.
   PubMed Web of Science ®Google Scholar
• Lansdorp, P. M., Dragowska, W. and Mayani, H. (1993). Ontogeny-related changes in proliferative potential of human hematopoietiv cells. J Exp Med, 178, 787–91.
   PubMed Web of Science ®Google Scholar
• Dexter, T. M., Allen, T. D. and Lajtha, L. G. (1977). Conditions controlling the proliferation of haemopoietic stem cells in vitro. J Cell Physiol, 91, 335–44.
   PubMed Web of Science ®Google Scholar
• Greenberger, J. S. (1984). Recent modifications of technique in human long-term bone marrow cultures. Kroc Found Ser, 18, 119–31.
   PubMedGoogle Scholar
• Greenberg, H. M., Parker, L. M., Newburger, P. E., Said, J., Cohen, G. I. and Greenberger, J. S. (1981). Corticosteroid dependence of continuous hemopoiesis in vitro with murine or human bone marrow. Hematol Bluttransfus, 26, 289–93.
   PubMedGoogle Scholar
• Anklesaria, P., Teixido, J., Laiho, M., Pierce, J. H., Greenberger, J. S. and Massague, J. (1990). Cell-cell adhesion mediated by binding of membrane-anchored transforming growth factor alpha to epidermal growth factor receptors promotes cell proliferation. Proc Natl Acad Sci USA, 87(9), 3289–93.
   PubMed Web of Science ®Google Scholar
• Anklesaria, P., FitzGerald, T. J., Kase, K., Ohara, A. and Greenberger, J. S. (1989). Improved hematopoiesis in anemic SI/SId mice by splenectomy and therapeutic transplantation of a hematopoietic microenvironment. Blood, 74(3), 1144–51.
   PubMed Web of Science ®Google Scholar
• Anklesaria, P., Teixido, J., Laiho, M., Pierce, J. H., Greenberger, J. S. and Massague, J. (1990). Cell-cell adhesion mediated by binding of membrane-anchored transforming growth factor alpha to epidermal growth factor receptors promotes cell proliferation. Proc Nat Acad of Sci USA, 87(9), 3289–93.
   PubMed Web of Science ®Google Scholar
• Perkins, S. and Fleischman, R. A. (1990). Stromal cell progeny of murine bone marrow fibroblast colony-forming units are clonal endothelial-like cells that express collagen IV and laminin. Blood, 75(3), 620–5.
   PubMed Web of Science ®Google Scholar
• Perkins, S. and Fleischman, R. A. (1988). Hematopoietic microenvironment. Origin, lineage, and transplantability of the stromal cells in long-term bone marrow cultures from chimeric mice. J Clin Invest, 81(4),1072–80.
   PubMed Web of Science ®Google Scholar
• Simmons, P. J., Gronthos, S., Zannettino, A., Ohta, S. and Graves, S. (1994). Isolation, characterization and functional activity of human marrow stromal progenitors in hemopoiesis. Prog Clin Biol Res, 389, 271–80.
   PubMedGoogle Scholar
• Drize, N. J., Surin, V. L., Gan, O. I., Deryugina, E. I. and Chertkov, J. L. (1992). Gene therapy model for stromal precursor cells of hematopoietic microenvironment. Leukemia, 6(3), 174S–175S.
   PubMedGoogle Scholar
• Anklesaria, P., Kase, K., Glowacki, J., Holland, C. A., Sakakeeny, M. A., Wright, J. A., FitzGerald, T. J., Lee, C. Y. and Greenberger, J. S. (1987). Engraftment of a clonal bone marrow stromal cell line in vivo stimulates hematopoietic recovery from total body irradiation. Proc Natl Acad Sci USA, 84(21), 7681–5.
   PubMed Web of Science ®Google Scholar
• van den Brink, M. R., Boggs, S. S., Herberman, R. B. and Hiserodt, J. C. (1990). The generation of natural killer (NK) cells from NK precursor cells in rat long-term bone marrow cultures. J Exp Med, 172, 303–13.
   PubMed Web of Science ®Google Scholar
• Vecchini, F., Delfino, D., Patrene, K. D., DeLeo, A., Lu, L., Herberman, R. B. and Boggs, S. S. (1993). Generation of natural killer (NK) cells from long-term cultures of mouse bone marrow. Nat Immun Cell Growth Regulation, 12, 1–16.
   Google Scholar
• Delfino, D. V., Patrene, K. D., DeLeo, A. B., DeLeo, R., Herberman, R. B. and Boggs, S. S. (1994). Role of CD44 in the development of Natural Killer cells from precursors in long-term Cultures of mouse bone marrow. J Immunol, 152, 5171–5179.
   PubMed Web of Science ®Google Scholar
• Kincade, P. W., Gimble, J. M., Dorheim, M. A., Cheng, Q., Medina, K., Wang, C. S., Jones, R., Koren, E. and Pietrangeli, C. (1990). Adipogenesis in a murine bone marrow stromal cell line capable of supporting B lineage lymphocyte growth and proliferation: biochemical and molecular characterization. European Journal of Immunology, February, 20(2), 379–87.
   PubMed Web of Science ®Google Scholar
• Whitlock, C. A. and Witte, O. N. (1982). Long-term culture of B lymphocytes and their precursors from murine bone marrow. Proc Natl Acad Sci USA, 79, 3608–12.
   PubMed Web of Science ®Google Scholar
• Witte, P. L., Robinson, M., Henley, A., Low, M. G., Stiers, D. L., Perkins, S., Fleischman, R. A. and Kincade, P. W. (1987). Relationships between B-lineage lymphocytes and stromal cells in long-term bone marrow cultures. Eur J Immunol, 17(10), 1473–84.
   PubMed Web of Science ®Google Scholar
• Waller, E. K., Olweus, J., Lund-Johansen, F., Huang, S., Nguyen, M., Guo, G. R. and Terstappen, L. (1995). The “common stem cell” hypothesis reevaluated: human fetal bone marrow contains separate populations of hematopoietic and stromal progenitors. Blood, 85(9), 2422–35.
   PubMed Web of Science ®Google Scholar
• Tavassoli, M. (1991). Embryonic and fetal hematopoiesis: an overview. Blood Cells, 1, 269.
   Google Scholar
• Detrich, H. W. 3rd, Kieran, M. W., Chan, F. Y., Barone, L. M., Yee, K., Rundstadler, J. A., Pratt, S., Ransom, D. and Zon, L. I. (1995). Intraembryonic hematopoietic cell migration during vertebrate development. Proc Natl Acad Sci USA, 92(23), 10713–7.
   PubMed Web of Science ®Google Scholar
• Barker, J. E. (1970). Embryonic mouse peripheral blood colony-forming units. Nature, 228, 1305.
   PubMed Web of Science ®Google Scholar
• Dzierzak, E. and Medvinsky, A. (1995). Mouse embryonic hematopoiesis. [Review] Trends in Genetics, 11, 359.
   PubMed Web of Science ®Google Scholar
• Moore, M. A. and Metcalf, D. (1970). Ontogeny of the haemopoietic system: yolk sac origin of in vivo and in vitro colony forming cells in the developing mouse embryo. Br J Haematol, 18, 279.
   PubMed Web of Science ®Google Scholar
• Barker, J. E., Keenan, M. A. and Raphals, L. (1969). Development of the mouse hematopoietic system. II. Estimation of spleen and liver “stem” cell number. J Cell Physiol, 74, 51.
   PubMed Web of Science ®Google Scholar
• Huang, H., Zettergren, L. D. and Auerbach, R. (1994). In vitro differentiation of B cells and myeloidcells from the early mouse embryo and its extraembryonic yolk sac [see comments]. Exp Hematol, 22, 19.
   PubMed Web of Science ®Google Scholar
• Zon, L. I. (1995). Developmental biology of hematopoiesis. [Review] Blood, 86(8), 2876–91.
   PubMed Web of Science ®Google Scholar
• Tavian, M., Coulombel, L., Luton, D., San Clemente, H., Dieterlen-Lievre, F. and Peault, B. (1996). Aorta-associated CD34+ hematopoietic cells in the early human embryo. Blood, 87, 67.
   PubMed Web of Science ®Google Scholar
• Huyan, A., Dommergues, M., Izac, B., Croisille, L., Katz, A., Vainchenker, W. and Coulombel, L. (1995). Characterization of hematopoietic progenitors from human yolk sacs and embryos. Blood, 86, 4474.
   PubMed Web of Science ®Google Scholar
• Nakano, T., Kodama, H. and Honjo, T. (1996). In vitro development of primitive and definitive erythrocytes from different precursors. Science, 272(5262), 722–4.
   PubMed Web of Science ®Google Scholar
• Huang, H. and Auerbach, R. (1993). Identification and characterization of hematopoietic stem cells from the yolk sac of the early mouse embryo. Proc Natl Acad Sci USA, 90, 10110.
   PubMed Web of Science ®Google Scholar
• Medvinsky, A. L., Gan, O. I., Semenova, M. L. and Samoylina, N. L. (1996). Development of day-8 colony-forming unit-spleen hematopoietic progenitors during early murine embryogenesis: spatial and temporal mapping. Blood, 87, 557.
   PubMed Web of Science ®Google Scholar
• Micklem, H. S. (1972). Cell proliferation in haematopoietic spleen colonies of mice: difference between colonies derived from injected adult bone marrow and foetal liver cells. Cell and Tissue Kinetics, 5, 159.
   PubMedGoogle Scholar
• Micklem, H. S., Ford, C. E., Evans, E. P., Ogden, D. A. and Papworth, D. S. (1972). Competitive in vivo proliferation of foetal and adult haematopoietic cells in lethally irradiated mice. J Cell Physiol, 79, 293.
   PubMed Web of Science ®Google Scholar
• Rebel, V. I., Miller, C. L., Thornbury, G. R., Dragowska, W. H., Eaves, C. J. and Lansdorp, P. M. (1996). A comparison of long-term repopulating hematopoietic stem cells in fetal liver and adult bone marrow from the mouse. Exp Hematol, 24, 638.
   PubMed Web of Science ®Google Scholar
• Jordan, C. T., McKearn, J. P. and Lemischka, I. R. (1990). Cellular and developmental properties of fetal hematopoietic stem cells. Cell, 61, 953.
   PubMed Web of Science ®Google Scholar
• Jordan, C. T. and Lemischka, I. R. (1990). Clonal and systemic analysis of long-term hematopoiesis in the mouse. Genes Dev, 4, 220.
   PubMed Web of Science ®Google Scholar
• McKearn, J. P., McCubrey, J. and Fagg, B. (1985). Enrichment of hematopoietic precursor cells and cloning of multipotential B-lymphocyte precursors. Proc Natl Acad Sci USA, 82, 7414.
   PubMed Web of Science ®Google Scholar
• Harrison, D. E. (1983). Long-term erythropoietic repopulating ability of old, young, and fetal stem cells. J Exp Med, 157, 1496.
   PubMed Web of Science ®Google Scholar
• Forrester, L. M., Bernstein, A., Rossant, J. and Nagy, A. (1991). Long-term reconstitution of the mouse hematopoietic system by embryonic stem cell-derived fetal liver. Proc Natl Acad Sci USA, 88, 7514.
   PubMed Web of Science ®Google Scholar
• Bell, S. and Zamoyska, R. (1991). Identification of thymocyte precursors in murine fetal liver. Eur J Immunol, 21, 2931.
   PubMed Web of Science ®Google Scholar
• Poggi, A., Sargiacomo, M., Biassoni, R., Pella, N., Sivori, S., Revello, V., Costa, P., Valtieri, M., Russo, G., Mingari, M. C., et at., (1993). Extrathymic differentiation of T lymphocytes and natural killer cells from human embryonic liver precursors. Proc Natl Acad Sci USA, 90, 4465.
   PubMed Web of Science ®Google Scholar
• Horton, W. A. (1990). The biology of bone growth. Growth Genet Horm, 6, 1–3.
   Google Scholar
• Fennie, C., Cheng, J., Dowbenko, D., Young, P. and Lasky, L. A. (1995). CD34+ endothelial cell lines derived from murine yolk sac induce the proliferation and differentiation of yolk sac CD34+ hematopoietic progenitors. Blood, 86, 4454–4467.
   PubMed Web of Science ®Google Scholar