Establishment of IL-5-Dependent Early B Cell Lines by Long-Term Bone Marrow Cultures

References

• Abramson S., Miller R. G., Phillips R. A. The identification in adult bone marrow of pluripotent and restricted stem cells of the myeloid and lymphoid systems. J. Exp. Med. 1977; 145: 1567–1579
   PubMedGoogle Scholar
• Clutterbuck E., Shields J. G., Gordon J., Smith S. H., Boyd A., Callard R. E., Campbell H. D., Young I. G., Sanderson C. J. Recombinant human interleukin 5 is an eosinophil differentiation factor but has no activity in standard human B cell growth factor analysis. Eur. J. Immunol. 1987; 17: 1743–1750
   PubMed Web of Science ®Google Scholar
• Coffman R. L. Surface antigen expression and immunoglobulin gene rearrangement during mouse pre-B cell development. Immunol. Rev. 1982; 69: 5–23
   PubMed Web of Science ®Google Scholar
• Collins L. S., Dorshkind K. A stromal cell line from myeloid long-term bone marrow cultures can support myelopoiesis and B lymphopoiesis. J. Immunol. 1987; 138: 1082–1089
   PubMed Web of Science ®Google Scholar
• Dexter T. M., Allen T. D., Lajtha L. G. Conditions controlling the proliferation of hematopoietic stem cells in vitro. J. Cell Physiol. 1977; 91: 335–344
   PubMed Web of Science ®Google Scholar
• Dorshkind K. In vitro differentiation of B lymphocytes from primitive hemopoietic precursors present in long-term bone marrow cultures. J. Immunol. 1986; 136: 422–429
   PubMedGoogle Scholar
• Harada N., Takahashi T., Matsumoto M., Kinashi T., Ohara J., Kikuchi Y., Koyama N., Severinson E., Yaoita Y., Honjo T., Yamaguchi N., Tominaga A., Takatsu K. Production of a monoclonal antibody useful in the molecular characterization of murine T cell-replacing factor (TRF) and B cell growth factor 11 (BCGF 11). Prof. Natl. Acad. Sci. USA 1987a; 84: 4581–4585
   Google Scholar
• Harada N., Matsumoto M., Takahashi T., Koyama N., Shimizu A., Honjo T., Tominaga A., Takatsu K. T cell-replacing factor (TRF) induces not only differentiation, but also increase in the levels of IL-2 receptor expression on activated B cells. Immunol. Lett. 1987b; 15: 205–215
   PubMed Web of Science ®Google Scholar
• Hardy R., Kishimoto T., Hayakawa K. Differentiation of B cell progenitors in vitro. generation of surface IgM+ B cells, including Ly-1+ B cells, from Thy-1- asialo-GM1+ cells in newborn liver. Eur. J. Immunol. 1987; 17: 1769–1774
   Google Scholar
• Hirayoshi K., Nishikawa S-I., Kina T., Hatanaka M., Habu S., Nomura T., Katsura Y. Immunoglobulin heavy chain gene diversification in the long-term bone marrow culture of normal mice and mice with severe combined immunodeficiency. Eur. J. Immunol. 1987; 17: 1051–1057
   Google Scholar
• Hunt P., Robertson D., Weiss D., Rennik D., Lee F., Witte O. W. A single bone marrow-derived stromal cell type supports the in vitro growth of early lymphoid and myeloid cells. Cell 1987; 48: 997–1007
   PubMed Web of Science ®Google Scholar
• Katsura Y., Amagai T., Kina T., Sado T., Nishikawa S-I. Two subpopulations of stem cells for T cell lineage. J. Immunol. 1987; 135: 3021–3027
   Google Scholar
• Kinashi T., Harada N., Severinson E., Tanabe T., Sideras P., Konishi M., Azuma C., Tominaga A., Bergstedt-Lindqvist S., Takahashi M., Matsuda F., Yaoita Y., Takatsu K., Honjo T. Cloning of complementary DNA encoding T cell-replacing factor and identity with B-cell growth factor II. Nature 1986; 324: 70–73
   PubMed Web of Science ®Google Scholar
• Landreth K. S., Rosse C., Clagett J. Myelogenous production and maturation of B lymphocytes in the mouse. J. Immunol. 1981; 127: 2027–2034
   PubMedGoogle Scholar
• Loughnan M. S., Takatsu K., Harada N., Nossal G. J. V. T cell-replacing factor (IL-5) acts as interleukin-2 receptor-inducing factor on murine splenic B cells. Proc. Natl. Acad. Sci. USA 1987; 84: 5399–5403
   PubMed Web of Science ®Google Scholar
• Matsumoto M., Tominaga A., Harada N., Takatsu K. Role of T cell-replacing factor (TRF) in the murine B cell differentiation: Induction of increased levels of expression of secreted type IgM mRNA. J. Immunol 1987; 138: 1826–1833
   Google Scholar
• Mita S., Harada N., Naomi S., Hitoshi Y., Sakamoto S., Akagi M., Tominaga A., Takatsu K. Receptors for T cell-replacing factor/interleukin 5 on B cells: Quantitation, specificity, and its implication. J. Exp. Med. 1988; 168: 863–878
   PubMed Web of Science ®Google Scholar
• Nakanishi K., Yoshimoto T., Katoh Y., Ono S., Matsui K., Hiroishi K., Noma T., Honjo T., Takatsu K., Higashino K., Hamaoka T. Both B151-TRF1 and interleukin 5 regulate immunoglobulin secretion and IL 2 receptor expression on a cloned B lymphoma line. J. Immunol. 1988; 140: 1168–1174
   Google Scholar
• Namen A. E., Lupton S., Hjerrild K., Wignall J., Mochizuki D. Y., Schmierer A., Mosley B., March C. J., Urdal D., Gillis S., Cosman D., Goodwin R. G. Stimulation of B-cell progenitors by cloned murine interleukin-7. Nature 1988; 333: 571–573
   PubMed Web of Science ®Google Scholar
• Nishikawa S-I., Kina T., Amagai T., Katsura Y. Early B cell precursors in long term bone marrow culture: selective development in the bone marrow of irradiated recipient. Eur. J. Immunol 1985; 15: 696–701
   Google Scholar
• Ogawa M., Nishikawa S., Ikuta K., Yamamura F., Naito M., Takahashi K., Nishikawa S-I. B cell ontogeny in murine embryo studied by a culture system with the monolayer of a stromal cell clone, ST2: B cell progenitor develops first in embryonal body rather than in yolk sac. EMBO J 1988; 7: 1337–1343
   PubMed Web of Science ®Google Scholar
• Palacios R., Henson T., Steinmetz M., McKearn J. P. Interleukin 3 supports growth of mouse pre-B cell clones in vitro. Nature 1984; 209: 126–131
   Google Scholar
• Palacios R., Karasuyama H., Rolink A. Ly1+ pro-B lymphocyte clones. Phenotype, growth requirement and differentiation in intro and in intro. EMBO J. 1987; 6: 3687–3693
   PubMed Web of Science ®Google Scholar
• Riggs J. L., Seiwald A. J., Burckhalter J. W., Downs C. M., Metcalf T. G. Isothiocyanate compounds as fluorescent labeling agents for immune serum. Amer. J. Pathol. 1958; 34: 1081–1098
   PubMed Web of Science ®Google Scholar
• Scatchard G. The attractions of proteins for small molecules and ions. Ann. NY Acad. Sci. 1949; 51: 660–672
   Web of Science ®Google Scholar
• Southern E. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol. 1975; 98: 503–517
   PubMed Web of Science ®Google Scholar
• Takatsu K. B cell growth and differentiation factos. Proc. Soc. Exp. Biol. Med. 1988; 188: 243–258
   Google Scholar
• Takatsu K., Kikuchi Y., Takahashi T., Honjo T., Matsumoto M., Harada N., Yamaguchi N., Tominaga A. Interleukin 5, a T cell derived B cell differentiation factor also induces cytotoxic T lymphocytes. Proc. Natl. Acad. Sci. USA 1987; 84: 4234–4238
   PubMed Web of Science ®Google Scholar
• Takatsu K., Tominaga A., Hamaoka T. Antigen-induced T cell-replacing factor (TRF). I. Functional characterization of TRF-producing helper T cell subset and genetic studies on TRF production. J. Immunol. 1980; 124: 2414–2422
   PubMed Web of Science ®Google Scholar
• Takatsu K., Tominaga A., Harada N., Mita S., Matsumoto M., Takahashi T., Kikuchi Y., Yamaguchi N. T cell-replacing factor (TRF)/interleukin 5 (IL-5): Molecular and functional properties. Immunol. Rev. 1988; 102: 107–135
   PubMed Web of Science ®Google Scholar
• Tominaga A., Matsumoto M., Harada N., Takahashi T., Kikuchi Y., Takatsu K. Molecular properties and regulation of mRNA expression for murine T cell-replacing factor (TRF)/interleukin 5 (IL-5). J. Immunol. 1988; 140: 1175–1181
   PubMed Web of Science ®Google Scholar
• Warren D. J., Moor M. A. S. Synergism among interleukin 1, interleukin 3, and interleukin 5 in the production of eosinophils from primitive hemopoietic stem cells. J. Immunol. 1988; 140: 94–99
   PubMed Web of Science ®Google Scholar
• Whitlock C. A., Witte O. N. Long-term culture of B lymphocytes and their precursors from murine bone marrow. Proc. Natl. Acad. Sci. USA 1982; 79: 3608–3612
   PubMed Web of Science ®Google Scholar
• Whitlock C. A., Tidmarsh G. F., Mueller-Sieburg C., Weissman I. L. Bone marrow stromal cell lines with lymphopoietic activity express high levels of a pre-B neoplasia-associated molecule. Cell 1987; 48: 1009–1021
   PubMed Web of Science ®Google Scholar
• Witte P. L., Robinson M., Henley A., Low M. G., Stiers D. L., Perkins L., Fleishman R. A., Kincade P. W. Relationships between B-lineage lymphocytes and stromal cells in long-term bone marrow cultures. Eur. J. Immunol. 1987; 17: 1473–1484
   PubMed Web of Science ®Google Scholar
• Yamaguchi Y., Suda T., Suda J., Eguchi M., Miura Y., Harada N., Tominaga A., Takatsu K. Purified interleukin-5 (IL-5) supports the terminal differentiation and proliferation of murine eosinophilic precursors. J. Exp. Med. 1988a; 167: 43–56
   PubMed Web of Science ®Google Scholar
• Yamaguchi Y., Hayashi Y., Sugama Y., Miura Y., Kasahara T., Kitamura S., Torisu M., Mita S., Tominaga A., Takatsu K., Suda T. Highly purified murine interleukin 5 (IL-5) stimulates eosinophil function and prolongs in vitro survival. IL-5 as an eosinophil chemotactic factor. J. Exp. Med. 1988b; 167: 1737–1742
   PubMed Web of Science ®Google Scholar
• Yokota T., Coffman R. L., Hagiwara H., Rennick D. M., Takebe Y., Yokota K., Gemmell L., Shrader B., Yang G., Meyerson P., Luh J., Hoy P., Pene J., Briere F., Banchereau J., Vries J. D., Lee F D., Arai N., Arai K. Isolation and characterization of lymphokine cDNA clones encoding murine and human IgA-enhancing factor and eosinophil colony stimulating factor activities: Relationship to interleukin 5. Proc. Natl. Acad. Sci. USA 1987; 84: 7388–7392
   PubMed Web of Science ®Google Scholar