Evidence for a Low-Affinity Interleukin-3 Receptor

References

• Benovic J. L., Strasser R. H., Caron M. G., Lefkowitz R. J. Beta-adrenergic receptor kinase: identification of a novel protein kinase that phosphorylates the agonist-occupied form of the receptor. Proc. Natl. Acad. Sci. USA 1988; 83: 2797–2801
   Web of Science ®Google Scholar
• Burgisser E. Radioligand-receptor binding studies: what's wrong with the Scatchard analysis?. TIPS 1984; 4: 142–144
   Google Scholar
• Chao M. V., Bothwell M. A., Ross A. H., Koprowski, Lanahan H.A.A, Buck C. R., Sehgal A. Gene transfer and molecular cloning of the human NGF receptor. Science 1986; 232: 518–521
   PubMed Web of Science ®Google Scholar
• Chen B. D., Clark C. R. Interleukin 3 (IL-3) regulates the in vitro proliferation of both blood monocytes and peritoneal exudate macrophages: synergism between a macrophage lineage-specific colony stimulating factor (CSF-1) and IL-3. J. Immunol. 1986; 137: 563–570
   PubMed Web of Science ®Google Scholar
• Cheng Y.-C., Prusoff W. H. Relationship between the inhibition constant (K) and the concentration of inhibitor which causes 50 per cent inhibition (Iw) of an enzymatic reaction. Biochem. Pharmacol. 1973; 22: 3099–3108
   PubMed Web of Science ®Google Scholar
• Cook W. D., Metcalf D., Nicola N. A., Burgess A. W., Walker F. Malignant transformation of a growth factor-dependent myeloid cell line by Abelson virus without evidence of an autocrine mechanism. Cell 1985; 41: 677–683
   PubMed Web of Science ®Google Scholar
• Dedhar S., Gaboury L., C P., Eaves C. Human granulocyte macrophage colony-stimulating factor is a growth factor active on a variety of cell-types of non-hemopoietic origin. Proc. Natl. Acad. Sci. USA 1988; 85: 9253–9257
   PubMed Web of Science ®Google Scholar
• Dixon R. A., Kobilka B. K., Strader D. J., Benovic J. L., Dohlman H. G., Frielle T., Bolanowski M. A., Bennett C. D., Rands E., Diehl R. E. Cloning of the gene and cDNA for mammalian beta-adrenergic receptor and homology with rhodopsin. Nature 1986; 321: 75–79
   PubMed Web of Science ®Google Scholar
• Fraker P. J., Speck J. C. Protein and cell membrane iodinations with a sparingly soluble chloramide, 1,3,4,6-tetrachloro-3a,6a-diphenylglycolurea. Biochem. Biophys. Res. Commun. 1978; 80: 849–857
   PubMed Web of Science ®Google Scholar
• Fraser J. K., Nicholls J., Coffey C., Lin F.-K., Berridge M. Down-modulation of high-affinity receptors for erythropoietin on murine erythroblasts by interleukin 3. Exp. Hematol. 1988; 16: 769–773
   PubMed Web of Science ®Google Scholar
• Greenberger J. S., Eckner R. J., Sakakeeny A., Marks P., Reid D., Nabel G., Hapel J. N., Ihle J. N., Humphries K. C. Interleukin 3-dependent hematopoietic progenitor cell lines. Fed. Proc. 1983; 42: 2762–2771
   PubMedGoogle Scholar
• Hatakeyama M., Tsudo M., Minamoto S., Kono T., Doi T., Miyata Y., Miyasaka M., Taniguchi T. Interleukin-2 receptor β chain gene: generation of three receptor forms by cloned human α and β chain cDNA's. Science 1989; 244: 551–556
   PubMed Web of Science ®Google Scholar
• Ihle J. N., Keller J, Greenberger J. S., Henderson L., Yette R. A., Morse HC, III. Phenotypic characteristics of cell lines requiring interleukin 3 for growth. J. Immunol. 1982; 129: 1377–1381
   PubMed Web of Science ®Google Scholar
• Ihle J. N., Keller J., Oroszlan S., Henderson L. E., Copeland T. D., Fitch F., Prystowsky M. B., Goldwasser E., Schrader J. W., Palaszynski E., Dy M., Lebel B. Biologic properties of homogeneous interleukin 3. J.Immunol 1983; 131: 282–287
   PubMed Web of Science ®Google Scholar
• Isfort R., Abraham R., Huhn R. D., Frackelton A. R., Ihle J. N. Stimulation of factor-dependent myeloid cell lines with interleukin 3 induces tyrosine phosphorylation of several cellular substrates. J. Biol. Chem. 1988a; 263: 19203–19209
   PubMed Web of Science ®Google Scholar
• Isfort R. J., Stevens D., May W. S., Ihle J. N. Interleukin 3 binds to a 140-kDa phosphotyrosine-containing cell surface protein. Proc. Natl. Acad. Sci. USA 1988b; 85: 7982–7986
   PubMed Web of Science ®Google Scholar
• Itoh N., Yonehara S., Schreurs J., Gorman D., Maruyama K., Yahara I., Arai K., Miyajima A. Molecular cloning of a cDNA encoding the murine interleukin-3 receptor reveals a consensus motif of a new cytokine receptor gene family. Science, (submitted)
   Google Scholar
• Kipreos E. T., Wang J. Y. J. Reversible dependence on growth factor interleukin-3 in myeloid cells expressing temperature sensitive v-abl oncogene. Oncogene Res. 1988; 2: 277–284
   PubMedGoogle Scholar
• Koyasu S., Tojo A., Miyajima A., Akiyama T., Kasuga M., Urabe A., Schreurs J., Arai K., Takaku F., Yahara I. Interleukin 3-specific tyrosine phosphorylation of a membrane glycoprotein of Mr150 000 in multi-factor-dependent myeloid cell lines. EMBO J 1987; 6: 3979–3984
   PubMed Web of Science ®Google Scholar
• Koyasu S., Nakauchi J., Kitamura K., Yonehara S., Okumura K., Tada T., Yahara I. Production of interleukin-3 and gamma interferon by an antigen-specific mouse suppressor T cell clone. J. Immunol. 1985; 134: 3130–3136
   PubMed Web of Science ®Google Scholar
• Leonard W. J., Depper J. M., Crabtree G. R., Rudikoff S., Pumphrey J., Robb R. J., Kronke M., Svetlik P. B., Pfeffer N, Waldmann T. A., Greene W. C. Molecular cloning and expression of cDNAs for the human interleukin-2 receptor. Nature 1984; 311: 626–631
   PubMed Web of Science ®Google Scholar
• Lowenthal J. W., Castle B. E., Christiansen J., Schreurs J., Rennick D., Arai N., Hoy P., Takebe Y., Howard M. Expression of high affinity receptors for murine inter-leukin-4 (BSF-1) on hemopoietic and non-hemopoietic cells. J. Immunol. 1988; 14: 456–464
   Google Scholar
• Maher P. A. Nerve growth factor induces protein-tyrosine phosphorylation. Proc. Natl. Acad. Sci. USA 1988; 85: 6788–6791
   PubMed Web of Science ®Google Scholar
• Mathey-Prevot B., Nabel G., Palacios R., Baltimore D. Abelson virus abrogation of interleukin 3 dependence in a lymphoid cell line. Mol. Cell. Biol. 1986; 6: 4133–4135
   PubMed Web of Science ®Google Scholar
• May W. S., Ihle J. N. Affinity isolation of the interleukin-3 surface receptor. Biochem. Biophys. Res. Commun. 1986; 135: 870–879
   PubMed Web of Science ®Google Scholar
• Mingari M. C, Gerosa F., Carra G., Accolla R. S., Moretta A., Zubler R. H., Waldmann T. A., Moretta L. Human interleukin-2 promotes proliferation of activated B cells via surface receptors similar to those of activated T cells. Nature 1984; 312: 641–643
   PubMed Web of Science ®Google Scholar
• Miyajima A., Schreurs, Otsu J., Kondo A., Arai K., Maeda S. Use of the silkworm, Bombyx mori, and an insect baculovirus vector for high level expression and secretion of biologically active mouse interleukin-3. Gene 1987; 58: 273–281
   PubMed Web of Science ®Google Scholar
• Miyajima A., Miyatake S., Schreurs J., DeVries J., Arai N., Yokota T., Arai K. Coordinate regulation of immune and inflammatory responses by T cell-derived lymphokines. FASEB J 1988; 2: 2462–2473
   PubMed Web of Science ®Google Scholar
• Miyajima A., Schreurs J., Wang H.-M., Maruyama K., Gorman D., Koyasu S., Yahara I., Wang J., Ohta Y., Arai K. Characterization of the mouse interleukin 3 receptor system. The Fourth International Congress on lmmunophar-macology. Pergamon Press, New York 1989, (in press)
   Google Scholar
• Morla A., Schreurs J., Miyajima A., Wang J. Y. J. Hematopoietic growth factors activate the tyrosine phosphorylation of distinct sets of proteins in interleukin-3-dependent murine cell lines. Mol. Cell. Biol. 1988; 8: 2214–2218
   PubMed Web of Science ®Google Scholar
• Mosmann T. Rapid colorimetric assays for cellular growth and survival: application to proliferation and cytotoxicity assays. J.Immunol. Methods 1983; 65: 55–63
   PubMed Web of Science ®Google Scholar
• Mosmann T. R., Abrams J. S., Arai K., Arai N., Bond M. W., Lee F. D., Miyajima A., Miyatake S., Rennick D., Schreurs J., Smith C. A., Takebe Y., Yokota T., Zurawski G., Zurawski S. M. Mouse interleukin-3; recombinant cDNA cloning, expression, and characterization, pp. 217–240. Recombinant Lymphokines and Their Receptors, S. Gillis. Marcel Dekker, New York 1987
   Google Scholar
• Mui A. L., Sorensen P. H. B., Kay R. J., Krystal G. Purification and characterization of the interleukin-3 receptor. Hemopoieses UCLA Symposia. Alan R. Liss, New York 1989; 120, (in press)
   Google Scholar
• Munson P. J. LIGAND: a computerized analysis of ligand binding data. Methods Enzymol. 1983; 92: 543–576
   PubMed Web of Science ®Google Scholar
• Munson P. J., Rodbard D. LIGAND: a versatile computerized approach for characterization of ligand-binding systems. Anal. Biochem. 1980; 107: 220–239
   PubMed Web of Science ®Google Scholar
• Murphy F., Sorensen P., Mui A., Krystal G. Interleukin-3 down-regulates its own receptor. Blood 1989; 73: 1180–1187
   PubMed Web of Science ®Google Scholar
• Nabel G. S., Galli J., Dvorak A. M., Dvorak H. F., Cantor H. Inducer T lymphocytes synthesize a factor that stimulates proliferation of cloned mast cells. Nature 1981; 291: 332–334
   PubMed Web of Science ®Google Scholar
• Nicola N. A., Metcalf D. Binding of iodinated multi-potential colony-stimulating factor (interleukin-3) to murine bone marrow cells. J.Cell Phys. 1986; 128: 180–188
   PubMed Web of Science ®Google Scholar
• Nicola N. A., Metcalf D. Binding, internalization, and degradation of 25I-multipotentia) colony-stimulating factor (interleukin-3) by FDCP-1 cells. Growth Factors 1988; 1: 29–39.
   PubMedGoogle Scholar
• Nicola N. A., Peterson L. Identification of distinct receptors for two hemopoietic growth factors (granulocyte colony-stimulating factor and multipotential colony-stimulating factor) by chemical cross-linking. J. Biol. Chem. 1986; 261: 12384–12389
   PubMed Web of Science ®Google Scholar
• Nikaido T., Shimizu A., Ishida N., Sabe H., Teshigawara K., Maeda M., Uchiyama T., Yodoi J., Honjo T. Molecular cloning of cDNA encoding human interleukin-2 receptor. Nature 1984; 311: 631–635
   PubMed Web of Science ®Google Scholar
• Palacios R., Henson G., Steinmetz M., McKearn J. P. Interleukin-3 supports growth of mouse pre-B-cell clones in vitro. Nature 1984; 309: 126–131
   PubMed Web of Science ®Google Scholar
• Palacios R., Kiefer M., Brockhaus M., Karjalainen K., Dembic Z., Kisielow N., von Boehmer H. Molecular, cellular, and functional properties of bone marrow T lymphocyte progenitor cells. J. Exp. Med. 1987; 166: 12–32
   PubMed Web of Science ®Google Scholar
• Palaszynski E. W., Ihle J. N. Evidence for specific receptors for interleukin 3 on lymphokine dependent cell lines established from long-term bone marrow cultures. J. Immunol. 1984; 132: 1872–1877
   PubMed Web of Science ®Google Scholar
• Park L., Friend D., Gillis S., Urdal D. L. Characterization of the cell surface receptor for a multilineage colony-stimulating factor CSF-2a. J. Biol. Chem 1986; 261: 205–210
   PubMed Web of Science ®Google Scholar
• Park L. S., Friend D., Price V., Anderson D., Singer J., Prickett K. S., Urdal D. L. Heterogeneity in human interleukin-3 receptors. J. Biol. Chem. 1989; 264: 5420–5427
   PubMed Web of Science ®Google Scholar
• Pierce J. H., Fiore P. P., Aaronson S. A., Potter M., Pumphrey J., Scott A., Ihle J. N. Neoplastic transformation of mast cells by Abelson-MuLV: abrogation of IL-3 dependence by a nonautocrine mechanism. Cell 1985; 41: 685–693
   PubMed Web of Science ®Google Scholar
• Pilch P. F., Czech M. Affinity cross-linking of peptide hormones and their receptors. Receptor Biochemistry and Methodology, Venter, Fraser. Alan R. Liss, New York 1984; 161–175
   Google Scholar
• Pluznik D. H., Cunningham R. E., Noguchi P. E. Colony-stimulating factor (CSF) controls proliferation of CSF-dependent cells by acting during the G, phase of the cell cycle. Proc. Natl. Acad. Sci. USA 1984; 81: 7451–7455
   PubMed Web of Science ®Google Scholar
• Prystowsky M. B., Often G., Naujokas M. F., Vardiman J., Ihle J. N., Goldwasser E., Fitch F. W. Multiple hemopoietic lineages are found after stimulation of mouse bone marrow precursor cells with interleukin 3. Am. J Pathol. 1986; 117: 171–179
   Web of Science ®Google Scholar
• Radeke M. J., Misko T. P., Hsu C., Herzenberg L. A., Shooter E. M. Gene transfer and molecular cloning of the rat nerve growth factor receptor. Nature 1987; 325: 593–597
   PubMed Web of Science ®Google Scholar
• Rennick D. M., Lee F. D., Yokota T., Arai K., Cantor H., Nabel G. J. A cloned MCGF cDNA encodes a multi-lineage hemotopoietic growth factor: multiple activities of interleukin 3. J. Immunol. 1985; 134: 910–914
   PubMed Web of Science ®Google Scholar
• Rennick D., Yang G., B L., Lee F. Control of hemopoiesis by a bone marrow stromal cell clone: lipopoly-saccharide- and interleukin-inducible production of colony stimulating factor. Blood 1987; 69: 682–691
   PubMed Web of Science ®Google Scholar
• Rennick D., Jackson J., Moulds C., Lee F., Yang G. IL-3 and stromal cell-derived factor synergistically stimulate the growth of pre-B cell lines cloned from long-term lymphoid bone marrow cultures. J. Immunol. 1989; 142: 161–166
   PubMed Web of Science ®Google Scholar
• Rodbard D. Mathematics of hormone-receptor interaction. I. Basic principles. Adv. Exp. Med. 1973; 36: 289–326
   PubMedGoogle Scholar
• Schlessinger J. The epidermal growth factor receptor as a multifunctional allosteric protein. Biochemistry 1988; 27: 3119–3123
   PubMed Web of Science ®Google Scholar
• Schreurs J., Miyajima A., Arai K., Sugawara W., Tanaka H., Ohta Y. 1652. Murine IL-3 receptor structure abst. FASEB J 1988; 2
   PubMed Web of Science ®Google Scholar
• Schreurs J., Sugawara M., Arai K., Ohta Y., Miyajima A. A monoclonal antibody with IL-3-like activity blocks IL-3 binding and stimulates tyrosine phosphorylation. J. Immunol. 1989; 142: 819–825
   PubMed Web of Science ®Google Scholar
• Schreurs J., Arai K., Miyajima A. Biochemistry of the detergent solubilized murine IL-3 receptor. Hemopoiesis UCLA Symposia, New. Alan R. Liss, York 1989; 120, (in press)
   Google Scholar
• Sorensen P., Farber N. M., Krystal G. Identification of the interleukin-3 receptor using an iodinatable, cleavable photoreactive cross-linking agent. J. Biol. Chem. 1986; 261: 9094–9097
   PubMed Web of Science ®Google Scholar
• Spalding D. M., Griffin J. A. Different pathways of differentiation of pre-B cell lines are induced by dendritic cells and T cells from different lymphoid tissues. Cell 1986; 44: 507–515
   PubMed Web of Science ®Google Scholar
• Takebe Y., Seiki M., Fujisawa J., Hoy P., Yokota K., Arai K., Hoshida M., Arai N. SRa promoter: an efficient and versatile mammalian cDNA expression system composed of the simian virus 40 early promoter and the R-U5 segment of human T-cell leukemia virus Type I long terminal repeat. Mol. Cell. Biol. 1987; 8: 466–472
   Web of Science ®Google Scholar
• Tsudo M., Uchiyama T., Uchino H. Expression of TAC antigen on activated normal human B cells. J. Exp. Med. 1984; 160: 612–617
   PubMed Web of Science ®Google Scholar
• Waldmann T.A., Goldman C. K., Ronn R. J., Depper J. M., Leonard W, Sharrow S. O., Buongiovanni K. F., Kors-meyer S. J., Greene W. C. Expression of interleukin 2 receptors on activated human B cells. J. Exp. Med. 1984; 160: 1450–1466
   PubMed Web of Science ®Google Scholar
• Wang H. M., Smith K. A. The interleukin 2 receptor. Functional consequences of its bimolecular structure. J. Exp. Med. 1987; 166: 1055–1069
   PubMed Web of Science ®Google Scholar
• Warren H. S., Hargreaves J., Hapel A. J. Some interleukin-3 dependent mast-cell lines also respond to interleukin-2. lymphokine Res. 1985; 4: 195–204
   PubMedGoogle Scholar
• Watson J. D., Eszes M., Overell R., Conlon P., Widmer M., Gillis S. Effect of infection with murine recombinant retroviruses containing the v-src oncogene on interleukin 2-and interleukin 3-dependent growth states. J. Immunol. 1987; 139: 123–129
   PubMed Web of Science ®Google Scholar
• Wheeler E. F., Askew D., May S., Ihle j. N., Sherr C. J. The v-fms oncogene induces factor independent growth and transformation of the interleukin 3 dependent myeloid cell line FDC-P1. Mol. Cell. Biol. 1987; 7: 1673–1680
   PubMed Web of Science ®Google Scholar