Regulation of chicken haemopoiesis by cytokines

Developmental and Comparative Immunology

Volumn 24, Issue 1, 2000, Pages 37-59

  Siatskas, Christopher ^a   Boyd, Richard ^a  

^a MONASH UNIVERSITY MEDICAL SCHOOL   (Australia)

Author keywords

Chicken; Cytokines; Haemopoiesis; Ontogeny; Stem progenitor cells

Indexed keywords

CYTOKINE; GROWTH FACTOR; INTERFERON; INTERLEUKIN 1; INTERLEUKIN 2; STEM CELL FACTOR; TRANSFORMING GROWTH FACTOR ALPHA; TRANSFORMING GROWTH FACTOR BETA;

CHICKEN; HEMATOPOIESIS; HEMATOPOIETIC SYSTEM; LYMPHOPOIESIS; NONHUMAN; ONTOGENY; PRIORITY JOURNAL; REVIEW; STEM CELL;

AVES; GALLUS GALLUS; MAMMALIA;

EID: 0033951390     PISSN: 0145305X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-305X(99)00051-8     Document Type: Review

References (200)

1. Moore M.A.S., Owen J.J.T. Chromosome marker studies on the development of the haemopoietic system in the chick embryo. Nature. 208:1965;989-990.
2. Moore M.A.S., Owen J.J.T. Stem cell migration in developing myeloid and lymphoid systems. Lancet. 23:1967;658-659.
3. Moore M.A.S., Owen J.J.T. Chromosome marker studies in the irradiated chick embryo. Nature. 215:1967;1081-1082.
4. Lassila O., Martin C., Toivanen P., Dieterlen-Liévre F. Erythropoiesis and lymphopoiesis in the chick yolk sac embyro chimaeras: contribution of yolk sac and intra-embryonic stem cells. Blood. 59:1982;377-381.
5. Hamburger V., Hamilton H.L. A series of normal stages in the development of the chick embryo. J. Morphol. 88:1951;49-92.
6. Szenberg A. Ontogeny of myelopoietic precursor cells in the chicken embryo. Benedict A.A. Avian immunobiology. Advances in experimental medical biology. vol. 88:1977;3-11 Plenum Press, New York, London.
7. Müller A.M., Medvinski A.L., Strouboulis J., Grosveld F., Dzierzak E.A. Development of hematopoietic stem cell activity in the mouse embryo. Immunity. 1:1994;291-301.
8. Moore M.A.S., Metcalf D. 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. 18:1970;279-296.
9. Huang H., Auerbach R. Identification and characterisation of hematopoietic stem cells from the yolk sac of the early mouse embryo. Proc. Natl. Acad. Sci. USA. 90:1993;10,110-10,114.
10. Reynaud C.A., Imhof B.A., Anquez V., Weill J.C. Emergence of committed B lymphoid progenitors in the developing chicken embryo. EMBO J. 11:1992;4349-4358.
11. Cumano A., Furlonger C., Paige C.J. Differentiation and characterization of B-cell precursors detected in the yolk sac and embryo body of embryos beginning at the 10- to 12-somite stage. Proc. Natl. Acad. Sci. USA. 90:1993;6429-6433.
12. Martin C., Beaupain D., Dieterlen-Liévre F. Developmental relationships between vitelline intra-embryonic haemopoiesis studied in the avian "yolk sac chimaeras" Cell Differentiation. 7:1987;115-130.
13. Lassila O., Eskola J., Toivanen P., Dieterlen-Liévre F. Lymphoid stem cells in the intra-embryonic mesenchyme of the chicken. Scand. J. Immunol. 11:1980;445-448.
14. Jotereau F.V., Houssaint E. Experimental studies in the migration and differentiation of primary lymphoid stem cells in the avian embryo. Solomon J.B., Horton J.D. Developmental immunobiology. 1977;123-130 Elsevier North Holland Biomedical Press, Amsterdam.
15. Dieterlen-Liévre F., Martin C. Diffuse intra-embryonic haemopoiesis in normal and chimeric avian development. Dev. Biol. 88:1981;180-191.
16. Cormier F., Dieterlen-Liévre F. The wall of the chick embryo aorta harbours M-CFC, G-CFC, GM-CFC and BFU-E. Development. 102:1988;279-285.
17. Dieterlen-Liévre F. Haemopoiesis during avian ontogeny. Poult. Sci. Rev. 5:1993;273-305.
18. Lassila O., Eskola J., Toivanen P. Pre-bursal stem cells in the intra-embryonic mesenchyme of the chick embryo at 7 days of incubation. J. Immunol. 123:1979;2091-2094.
19. Dieterlen-Liévre F. On the origin of haemopoietic stem cells in the avian embryo: an experimental approach. J. Embryol. Exp. Morphol. 33:1975;607-619.
20. Lassila O., Eskola J., Toivanen P., Martin C., Dieterlen-Liévre F. The origin of lymphoid stem cells studied in chick yolk sac-embryo chimaeras. Nature. 272:1978;353-354.
21. Ramanoff A.L. The avian embryo. 1960;Macmillan Company, New York.
22. Beaupain D., Martin C., Dieterlen-Liévre F. Are developmental hemoglobin changes related to the origin of stem cells and the site of erythropoiesis? Blood. 53:1979;212-225.
23. Nakano T., Kodama H., Honjo T. In vitro development of primitive and definitive erythrocytes from different precursors. Science. 272:1996;722-724.
24. Godin I.E., Garcia-Porrero J.A., Coutinho A., Dieterlen-Liévre F., Marcos M.A. Para-aortic splanchnopleura from early mouse embryos contains B1a progenitors. Nature. 364:1993;67-70.
25. Medvinski A.L., Samoylina N.L., Müller A.M., Dzierzak E.A. An early pre-liver intra-embryonic source of CFU-S in the developing mouse. Nature. 364:1993;64-66.
26. Godin I., Dieterlen-Liévre F., Cumano, A. Emergence of multipotential hemopoietic cells in the yolksac paraaortic splanchnopleura in mouse embryos, beginning at 8.5 days postcoitus. Proc. Natl. Acad. Sci. USA. 92:1995;737-777.
27. Cumano A., Dieterlen-Liévre F., Godin I. Lymphoid potential probed before circulation in mouse is restricted to caudal intraembryonic splanchnopleura. Cell. 86:1996;907-916.
28. + hematopoietic cells in the early human embryo. Blood. 87:1996;67-72.
29. Delanney L.E., Ebert J.D. On the chick spleen: origin, patterns of normal development and their experimental modification. Contrib. Embryol. 255:1962;57-86.
30. Yassine F., Fedecka-Bruner B., Dieterlen-Liévre F. Ontogeny of the chick embryo spleen - a cytological study. Cell Differ. Dev. 27:1989;29-45.
31. Dieterlen-Liévre F., Beaupain D., Martin C. Origin of erythropoietic stem cells in avian development: shift from the yolk sac to an intraembryonic site. Ann. Immunol. 127C:1976;857-863.
32. Payne L.M., Powell P.C. The lymphoid system. Freeman B.M. Physiology and biochemistry of the domestic fowl. 1984;278-321 Academic Press, Florida.
33. Keller G., Havele C., Longenecker M., Diener E. Ontogeny of hemopoietic colony forming units in the chicken embryo spleen. Benedict A.A. Avian immunobiology. Advances in experimental medical biology. vol. 88:1977;13-27 Plenum Press, New York, London.
34. Till J.E., McCulloch E.A. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiat. Res. 14:1961;213-222.
35. Nicolas-Bolnet C., Yassine F., Cormier F., Dieterlen-Liévre F. Developmental kinetics of hemopoietic progenitors in the avian embryo spleen. Exp. Cell Res. 196:1991;294-301.
36. Eskola J., Toivanen A. Cell transplantation into immunodeficient chicken embryos. Reconstituting capacity of cells from the bursa of Fabricius, spleen, bone marrow, thymus liver of 18 day old embryos. Cell. Immunol. 26:1976;68-77.
37. Toivanen A., Eskola J., Toivanen P. Restorative effects of different embryonic cells transplanted into immunodeficient chick embryos. Ann. Immunol. 127C:1976;923-929.
38. Houssaint E., Lassila O., Vainio O. Bu-1 antigen expression as a marker for B cell precursors in chicken embryos. Eur. J. Immunol. 19:1989;239-243.
39. Göbel T.W.F., Chen C.L.H., Shrimpf J., Grossi C.E., Bernot A., Bucy R.P., et al. Characterization of avian natural killer cells and their intracellular CD3 protein complex. Eur. J. Immunol. 24:1994;1685-1691.
40. Samarut J., Nigon V. Properties and development of erythropoietic stem cells in the chick embryo. J. Embryol. Exp. Morphol. 36:1976;247-260.
41. Broxmeyer H.E., Cooper S., Lu L., Hangoc G., Anderson D., Cosman D., et al. Effect of murine mast cell growth factor (c-kit proto-oncogene ligand) on colony formation by human marrow hematopoietic progenitor cells. Blood. 77:1991;2142-2149.
42. Tavassoli M. Embryonic fetal hemopoiesis: an overview. Blood Cells. 1:1991;269-281.
43. Bell S.E., Zamoyska D. Identification of thymocyte precursors in murine fetal liver. Eur. J. Immuol. 21:1991;2931-2936.
44. Kantor A.B., Stall A.M., Adams S., Herzenberg L.A. Differential development of progenitor activity for three B-cell lineages. Proc. Natl. Acad. Sci. USA. 89:1992;3320-3324.
45. Wong G.K., Cavey M.J. Development of the liver in the chicken embryo. Erythropoietic and granulopoietic cells. Anat. Rec. 235:1993;131-143.
46. Ratcliffe M.J.H. Development of the avian B lymphocyte lineage. Crit. Rev. Poult. Biol. 2:1989;207-234.
47. Le Douarin N.M., Dieterlen-Liévre F., Oliver P.D. Ontogeny of primary lymphoid organs and lymphoid stem cells. Am. J. Anat. 170:1984;261-299.
48. Houssaint E., Belo M., Le Douarin N.M. Investigations on cell lineage tissue interactions in the developing bursa of Fabricius through interspecific chimaeras. Dev. Biol. 53:1976;250-264.
49. Hemmingsson E.J., Alm G.V. Migration of stem cells from the yolksac to the thymus and bursa of Fabricius in the chicken embryo. Acta. Pathol. Microbiol. Scand. Section A. 81:1973;79-84.
50. Weber W.T., Mausner R. Migration patterns of avian embryonic bone marrow cells and their differentiation to functional T- and B-cells. Benedict A.A. Avian immunobiology. Advances in experimental medical biology. vol. 88:1977;47-59 Plenum Press, New York, London.
51. Le Douarin N.M., Jotereau F.V. The homing of lymphoid stem cells to the thymus and bursa of Fabricius as studied in avian embryo chimaeras. Congès Paris Juillet 1980. Fougereau M., Dausset J. Immunology. 1980;285-302 Academic Press, London.
52. Houssaint E., Mansikka A., Vainio O. Early separation of B and T lymphocyte precursors in chick embryo. J. Exp. Med. 174:1991;397-406.
53. Ratcliffe M.J.H., Lassila O., Pink J.R.L., Vainio O. Avian B cell precursors: surface immunoglobulin expression is an early, possibly bursa-independent event. Eur. J. Immunol. 16:1991;129-133.
54. Palojoki E., Lassila O., Jalkanen S., Toivanen P. Involvement of the avian μ heavy chain in recolonisation of the bursa of Fabricius. Scand. J. Immunol. 36:1992;251-259.
55. Toivanen P., Toivanen A., Good R.A. Ontogeny of bursal function in chicken. Embryonic stem cell for humoral immunity. J. Immunol. 109:1972;1058-1070.
56. Toivanen P., Toivanen A. Bursal and post bursal stem cells in chicken. Functional characteristics. Eur. J. Immunol. 3:1973;585-595.
57. Toivanen P., Toivanen A., Linna T.J., Good R.A. Ontogeny of bursal function in chicken. Post embryonic stem cell for humoral immunity. J. Immunol. 109:1972;1071-1080.
58. Kadish J.L., Basch R.S. Thymic regeneration after lethal irradiation: evidence for an intra-thymic radioresistant T cell precursor. J. Immunol. 114:1975;452-458.
59. Meijne E.J.M., Ria J.M., Groenewegen W.D.W.V., Ploemacher R.E., Vos O., David J.A.G., et al. The effects of x-irradiation on hematopoietic stem cell compartments in the mouse. Exp. Hematol. 19:1991;617-623.
60. Dieterlen-Liévre F., Pardanaud L., Yassine F., Cormier F. Early haemopoietic stem cells in the avian embryo. J. Cell. Sci. 10:(Suppl.):1988;29-44.
61. Houssaint E. Cell lineage segregation during bursa of Fabricius ontogeny. J. Immunol. 138:1987;3626-3634.
62. Davidson W.F., Pierce J.H., Rudikoff S., Morse H.C. Relationships between B cell and myeloid differentiation. Studies with a B lymphocyte progenitor line, HAFTL-1. J. Exp. Med. 168:1988;389-407.
63. Boyd A.W., Schrader J.W. Derivation of macrophage like lines from the pre-B lymphoma ABLS 8.1 using 5-azacytidine. Nature. 297:1982;691-693.
64. Martin M., Strasser A., Baumgarth N., Cicuttini F.M., Welch K., Salvaris E., Boyd A.W. A novel cellular model (SPGM 1) of switching between the pre-B cell and myelomonocytic lineages. J. Immunol. 150:1993;4395-4406.
65. Klinken S.P., Alexander W.S., Adams J.M. Hemopoietic lineage switch: v-raf oncogene converts Eμ-myc transgenic B cells into macrophages. Cell. 53:1988;857-867.
66. Cumano A., Paige C.J., Iscove N.N., Brady G. Bipotential precursors of B cells and macrophages in murine fetal liver. Nature. 356:1992;612-614.
67. Borrello M.A., Phipps R.P. Fibroblasts support outgrowth of splenocytes simultaneously expressing B lymphocyte and macrophage characteristics. J. Immunol. 155:1995;4155-4161.
68. Lindemann G.J., Adams J.M., Cory S., Harris A.W. B-lymphoid to granulocytic switch during hematopoiesis in a transgenic mouse strain. Immunity. 1:1994;517-527.
69. Metcalf D., Lindemann G.J., Nicola N. Analysis of hematopoiesis in max 41 transgenic mice that exhibit sustained elevations of blood granulocytes and monocytes. Blood. 85:1995;2364-2370.
70. Langdon W.Y., Harris A.W., Cory S., Adams J.M. The c-myc oncogene perturbs B lymphocyte development in Eμ-myc transgenic mice. Cell. 47:1986;11-18.
71. Wu L., Antica M., Johnson G.R., Scollay R., Shortman K. Developmental potential of the earliest precursor cells from the adult mouse thymus. J. Exp. Med. 174:1991;1617-1627.
72. Ardavin C., Wu L., Shortman K. Thymic dendritic cells and T cells develop simultaneously in the thymus from a common precursor population. Nature. 362:1993;761-763.
73. Jotereau F.V., Le Douarin N.M. The developmental relationship between osteocytes and osteoclasts: a study using the quail-chick nuclear marker in endochondral ossification. Dev. Biol. 63:1978;253-265.
74. Corbel C., Pouquié O., Cormier F., Vaigot P., LeDouarin N.M. BEN/SCI/DM-GRASP, a homophilic adhesion molecule, is required for in vitro myeloid colony formation in avian haemopoietic progenitors. Proc. Natl. Acad. Sci. USA. 93:1996;2844-2849.
75. + hemopoietic progenitors. J. Cell. Biol. 135:1996;1655-1668.
76. Bäck O., Bäck E., Hemmingsson E.J., Liden S., Linna T.J. Migration of bone marrow cells to the bursa of Fabricius and the spleen in the chicken. Scand. J. Immunol. 2:1973;357-365.
77. Dunon D., Kaufman J., Salomonsen J., Skjoedt K., Vainio O., Thiery J.P., et al. T-cell precurors migration towards β2-microglobulin is involved in thymus colonization of the chicken embryos. EMBO J. 9:1990;3315-3352.
78. Dieterlen-Liévre F. Birds. Rowley A.F., Ratcliffe N.A. Invertebrate blood cells. 1988;257-336 Cambridge University Press, New York.
79. Leutz A., Beug H., Graf T. Purification and characterization of cMGF, a novel chicken myelomonocytic growth factor. EMBO J. 3:1984;3191-3197.
80. Beug H., Hayman M.J., Graf T. Myeloblasts transformed by the avian acute leukemia virus E26 are hormone-dependent for growth and for expression of a putative myb containing protein, p35 E26. EMBO J. 1:1982;1069-1073.
81. Leutz A., Beug H., Walter C., Graf T. Hematopoietic growth factor glycosylation. J. Biol. Chem. 263:1988;3905-3911.
82. Leutz A., Damm K., Sterneck E., Kowenz E., Ness S., Frank R., et al. Molecular cloning of the chicken myelomonocytic growth factor (cMGF) reveals relationship to interleukin 6 and granulocyte colony stimulating factor. EMBO J. 8:1989;175-181.
83. York J.J., Strom A.D.G., Connick T.E., McWaters P.G., Boyle D.B., Lowenthal J.W. In vivo effects of chicken myelomonocytic growth factor. Delivery via a viral vector. J. Immunol. 156:1996;2991-2997.
84. Lowenthal J.W., York J.J., O'Neil T.E., Steven R.A., Strom D.G., Digby M.R. Potential use of cytokine therapy in poultry. Vet. Immunol. Immunopathol. 63:1998;191-198.
85. Nicola N.A. Why do hemopoietic growth factor receptors interact with each other? Immunol. Today. 8:1987;134-140.
86. Woldman I., Mellitzer G., Kieslinger M., Buchhart D., Meinke A., Beug H., et al. STAT 5 involvement in the differentiation reponse of primary chicken myeloid cell progenitors to myelomonocytic growth factor. J. Immunol. 159:1997;877-886.
87. Azam M., Erdjument-Bromage H.E., Kreider B.L., Xia M., Quelle F., Basu R., et al. Interleukin-3 signals through multiple isoforms of Stat5. EMBO J. 14:1995;1402-1411.
88. Baramand-Pour F., Meinke A., Eilers A., Gouilleux F., Groner B., Decker T. Colony stimulating factors and interferon-γ activate a protein related to MGF-STAT 5 to cause formation of the differentiation-induced factor in myeloid cells. FEBS. Lett. 360:1995;29-33.
89. Gouilleux F., Pallard C., Dusanter-Fourt I., Wakao H., Haldosen L.A., Norstedt G., et al. Prolactin, growth hormone, erythropoietin and granulocyte-macrophage colony stimulating factor induce MGF-STAT 5 binding activity. EMBO J. 14:1995;2005-2013.
90. Issacs A., Lindenmann J. Virus intereference. I. The Interferon. Proc. R. Soc. Lond [Biol.]. 147:1957;258-267.
91. Sekellick M.J., Ferrino A.F., Hopkins D.A., Marcus P.I. Chicken interferon gene: cloning, expression, and analysis. J. Interferon. Res. 14:1994;71-79.
92. Digby R.M., Lowenthal J.M. Cloning expression of the chicken interferon-γ gene. J. Interferon Cytokine Res. 15:1995;939-945.
93. Lillehoj H.S., Kaspers B., Jenkins M.C., Lillehoj E.P. Avian interferon and interleukin-2. A review by comparison with mammalian homologues. Poultry Sci. Rev. 4:1992;67-85.
94. Kohase M., Moriya H., Sato T.A., Kohno S., Yamazaki S. Purification and characterization of chicken interferon induced by viruses. J. Gen. Virol. 67:1986;215-218.
95. Sekellick M.J., Marcus P.I. Induction of high titer chicken interferon. Methods. Enzymol. 119:1986;115-125.
96. Onaga H., Tajima M., Ishii T. Activation of macrophages by culture fluid of antigen-stimulated spleen cells collected from chickens immunised with Eimeria tenella. Vet. Parasitol. 13:1983;1-11.
97. von Bülow V., Weiler H., Klasen A. Activating effects of interferons, lymphokines and viruses on cultured chicken macrophages. Avian Pathol. 13:1984;621-637.
98. Lillehoj H.S., Kang S.Y., Keller L., Sevoian M. Eimeria tenella and Eimeria acervulina: lymphokines secreted by an avian T cell lymphoma or by sporozoite-stimulated immune lymphocytes protect chickens against avian coccidiosis. Exp. Parasitol. 69:1989;54-64.
99. Krempien U., Redmann I., Jungwirth C. Purification of chick interferon by zinc chelate affinity chromatography and sodium dodecylsulphate-polyacrylamide gel electrophoresis. J. Interferon Res. 5:1985;209-214.
100. Pusztai R., Tarodi B., Beladi I. Production and characterization of interferon induced in chicken leukocytes by concanavalin A. Acta Virol. 30:1986;131-136.
101. Fredericksen T.L., Sharma J.M. Purification of avian T cell growth factor and immune interferon using gel filtration high resolution chromatography. Weber W.T., Ewert D.L. Avian immunology. Progress in clinical biological research. vol. 238:1987;145-156 Alan R. Liss, New York.
102. Dijmans R., Creemers J., Billiau A. Chicken macrophage activation by interferon: do birds lack the molecular homologue of mammalian interferon-γ? Vet. Immunol. Immunopathol. 26:1990;319-332.
103. Yip Y.K., Barrowclough B., Urban C., Vilcek J. Purification of two subspecies of human γ (immune) interferon. Proc. Natl. Acad. Sci. USA. 78:1982;1820-1824.
104. Schultz U., Kaspers B., Rinderle C., Sekellick M.J., Markus P.I., Staeheli P. Recombinant chicken interferon: a potent antiviral agent that lacks intrinsic macrophage activating factor activity. Eur. J. Immunol. 25:1995;847-851.
105. Schultz U., Rinderle C., Sekellick M.J., Markus P.I., Staeheli P. Recombinant chicken interferon from Escherichia coli and transfected COS cells is biologically active. Eur. J. Biochem. 229:1995;73-76.
106. Lowenthal J.W., Digby M.R., York J.J. Production of interferon-γ by chicken T cells. J. Interferon Cytokine Res. 15:1995;933-938.
107. Sekellick M.J., Lowenthal J.W., O'Nell T.E., Markus P.I. Chicken interferon types I and II enhance synergistically the antiviral state and nitric oxide secretion. J. Interferon Cytokine Res. 18:1998;407-414.
108. Song K.D., Lillehoj H.S., Choi K.D., Zarlenga D., Han J.Y. Expression and functional characterisation of recombinant chicken interferon-gamma. Vet. Immunol. Immunopathol. 58:1997;321-333.
109. Lillehoj H.S., Choi K.D. Recombinant chicken interferon-gamma-mediated inhibition of Eimeria tenalla development in vitro and reduction of oocyst production and body weight loss following Eimeria acervulina infection. Avian Dis. 42:1998;307-314.
110. Zhou J.-H., Ohtaki M., Sakurai M. Sequence of a cDNA encoding chicken stem cell factor. Gene. 127:1993;269-270.
111. Anderson D.M., Williams D.E., Tushinski R., Gimpel S., Eisenman J., Cannizzaro L.A., et al. Alternative splicing of mRNAs encoding human mast cell growth factor localization of the gene to chromosome 12q22-q24. Cell Growth Differ. 2:1991;373-378.
112. Martin F.H., Suggs S.V., Langley K.E., Lu H.S., Ting J., Okino K.H., et al. Primary structure and functional expression of rat and human stem cell factors DNAs. Cell. 63:1990;203-211.
113. Bartunek P., Pichlikova L., Stengl G., Boehmelt G., Martin F.H., Beug H., et al. Avian stem cell factor (SCF): production and characterization of the recombinant his-tagged SCF of chicken and its neutralizing antibody. Cytokine. 8:1996;14-20.
114. Hayman M.J., Meyer S, Martin F., Steinlein P., Beug H. Self-renewal and differentiation of normal avian erythroid progenitor cells: regulatory roles of the TGF-α/c-ErbB and SCF/c-kit receptors. Cell. 74:1993;157-169.
115. Larsen J., Meyer S., Steinlein P., Beug H., Hayman M.J. Transformation of chicken bone marrow cells by the v-ski oncogene. Oncogene. 8:1993;3221-3228.
116. Steinlein P., Wessely O., Meyer S, Deiner E.-M., Hayman M., Beug H. Primary, self-renewing erythroid progenitors develop through activation of both tyrosine kinase and steroid hormone receptors. Curr. Biol. 5:1995;191-204.
117. Lahav R., Lecoin L., Ziller C., Nataf V., Carnahan J.F., Martin F.H., et al. Effect of the steel gene product on melanogenesis in avian neural crest cell cultures. Differentiation. 58:1994;133-139.
118. Van't Hof R.J., von Lindern M., Nijweide P.J., Beug H. Stem cell factor stimulates chicken osteoclast activity in vitro. FASEB J. 11:1997;287-293.
119. Carnahan J.F., Patel D.R., Miller J.A. Stem cell factor is a neurotrophic factor for neural crest-derived chick sensory neurons. J. Neurosci. 14:1994;1433-1440.
120. Sasaki E., Okamura H.H., Chikamune T., Kanai Y., Watanabe A., Mitsuru N., et al. Cloning and expression of the chicken c-kit proto-oncogene. Gene. 128:1993;257-261.
121. Galli S.J., Zsebo K.M., Geissler E.N. The kit ligand, stem cell factor. Adv. Immunol. 55:1994;1-98.
122. Soler C., Carpenter G. Transforming growth factor-α (TGF-α). Nicola N.A. Guidebook to cytokines and their receptors. 1994;194-197 Oxford University Press, Oxford, New York, Tokyo.
123. Waltz T.M., Malm C., Nishikawa B.K., Wasteson A. Transforming growth factor-α (TGF-α) in human marrow: demonstration of TGF-α in erythroblasts and eosinophilic precursors and of epidermal growth factor receptors in blastlike cells of myelomonocytic origin. Blood. 85:1995;2385-2392.
124. Ullrich A., Coussens L., Hayflick J.S., Dull T.J., Gray A., Tam A.W., et al. Human epidermal growth factor receptor cDNA sequence and aberrant expression of the amplified gene in A431 epidermoid carcinoma cells. Nature. 309:1984;418-425.
125. Pain B., Woods C.M., Saez J., Flickinger T., Raines M., Peyrol S., et al. EGF-R as a hemopoietic growth factor receptor: the c-erbB product is present in chicken erythrocytic progenitors and controls their self-renewal. Cell. 65:1991;37-46.
126. Downward J., Yarden Y., Mayes E., Scrace G., Totty N., Stockwell P., et al. Close similarity of epidermal growth factor receptor and v-erbB oncogene protein sequences. Nature. 307:1984;521-526.
127. Schroeder C., Gibson L., Nordström C., Beug H. The estrogen receptor co-operates with the TGF-α receptor (c-erbB) in regulation of chicken erythroid progenitor self-renewal. EMBO J. 12:1993;951-960.
128. Roberts A.B., Sporn M.B. The transforming growth factor β's. Sporn M.B., Roberts A.B. Peptide growth factors their receptors. 1990;419-472 Springer-Verlag, Berlin, New York.
129. Gitelman S.E., Derynck R. Transfoming growth factor β (TGF-β). Nicola N.A. Guidebook to cytokines and their receptors. 1994;223-226 Oxford University Press, Oxford, New York, Tokyo.
130. Cheifetz S., Weatherbee J.A., Tsang M.L., Andersen J.K., Mole J.E., Lucas R., Massagué J. The transforming growth factor-beta system, a complex pattern of cross reactive ligands and receptors. Cell. 48:1987;409-415.
131. Jakowlew S.B., Dillard P.J., Kondaiah P., Sporn M.B., Roberts A.B. Complementary deoxyribonucleic acid cloning of a novel transforming growth factor-β, messenger ribonucleic acid from chick embryo chondrocytes. Molec. Endocrinol. 2:1988;747-755.
132. Jakowlew S.B., Dillard P.J., Sporn M.B., Roberts A.B. Complementary deoxyribonucleic acid cloning of a messenger ribonucleic acid encoding transforming growth factor β4 from chicken embryo chondrocytes. Molec. Endocrinol. 2:1988;1186-1195.
133. Jakowlew S.B., Dillard P.J., Sporn M.B., Roberts A.B. Complementary deoxyribonucleic acid cloning of an mRNA encoding transforming growth factor-β2 from chicken embryo chondrocytes. Growth Factors. 2:1990;123-133.
134. Jakowlew S.B., Dillard P.J., Winokur T.S., Flanders K.C., Sporn M.B., Roberts A.B. Expression of transforming growth factors-β's 1-4 in chicken embryo chondrocytes myocytes. Dev. Biol. 143:1991;135-148.
135. Jakowlew S.B., Ciment G., Tuan R.S., Sporn M.B., Roberts A.B. Expression of transforming growth factor-β2 and β3 mRNAs proteins in the developing chicken embryo. Differentiation. 55:1994;105-118.
136. Kondaiah P., van Obberghen-Schilling E., Ludwig R., Dhar R., Sporn M.B., Melton D.A. cDNA cloning of porcine TGF-beta: evidence for alternative splicing. J. Biol. Chem. 263:1988;18,313-18,317.
137. Keller J.R., Sing G.K., Ellingsworth L.R., Ruscetti F.W. Transforming growth factor-β: possible roles in the regulation of normal and leukemia hematopoietic cell growth. J. Cell. Biochem. 39:1989;79-84.
138. Sugano S., Stoeckle M.Y., Hanufusa H. Transformation by Rous-sarcoma virus induces a novel gene with homology to a mitogenic platelet protein. Cell. 49:1987;321-328.
139. Stoeckle M.Y., Barker K.A. Two burgeoning families of platelet factor 4-related proteins: mediators of the inflammatory response. New Biol. 22:1990;313-323.
140. Martins-Green M., Stoeckle M., Hampe A., Wimberly S., Hanafusa H. The 9E3/CEF4 cytokine: kinetics of secretion, processing by plasmin, and interaction with extracellular matrix. Cytokine. 8:1996;448-459.
141. Gonneville L., Martins T.J., Bérard P.-A. Complex expression pattern of the CEF-4 cytokine in transformed and mitogenically stimulated cells. Oncogene. 6:1991;1825-1833.
142. Barker K.A., Hampe A., Stoeckle M.Y., Hanafusa H. Transformation associated cytokine 9E3/CEF4 is chemotactic for chicken peripheral blood mononuclear cells. J. Virol. 67:1993;3528-3533.
143. Bagglioni M.A., Walz A., Kunkel S.L. NAP/IL-8, a novel cytokine that activates neutrophils. J. Clin. Invest. 84:1989;1045-1049.
144. Hayari Y., Schauenstein K., Globerson A. Avian lymphokines, II: interleukin-1 activity in supernatants of stimulated adherent splenocytes of chickens. Dev. Comp. Immunol. 6:1982;785-789.
145. Klasing K.C., Peng R.K. Influence of cell sources, stimulating agents, and incubation conditions on release of interleukin-1 from chicken marocrophages. Dev. Comp. Immunol. 11:1987;385-394.
146. Klasing K.C. Avian interleukin-1: immunological and physiological functions. Proceedings of the Thirty-sixth Western Poultry Disease Conference. Cooperative extension, University of California, Davis, CA. 1987;82-84.
147. Klasing K.C., Peng R.K. Monokine-like activities released from a chicken macrophage line. Anim. Biotech. 1:1990;107-120.
148. Klasing K.C., Laurin D.E., Peng R.K., Fry D.M. Immunologically mediated growth depression in chicks: influence of feed intake, corticosterone, and interleukin-1. J. Nutr. 117:1987;1629-1637.
149. Weining K.C., Sick C., Kaspers B., Staheli P. A chicken homologue of mammalian interleukin-1β: cDNA cloning and purification of active recombinant protein. Eur. J. Biochem. 258:1998;994-1000.
150. Guida S., Heguy A., Melli M. The chicken IL-1 receptor: differential evolution of the cytoplasmic extracellular domains. Gene. 111:1992;239-243.
151. Schauenstein K., Globerson A., Wick G. Avian lymphokines: I. Thymic cell growth factor in supernatants of mitogen stimulated chicken spleen cells. Dev. Comp. Immunol. 6:1982;533-540.
152. Schnetzler M., Oommen A., Nowak J.S., Franklin R.M. Characterization of chicken T cell growth factor. Eur. J. Immunol. 13:1983;560-568.
153. H2 cells: differential patterns of lymphokine secretion lead to different functional properties. Ann. Rev. Immunol. 7:1989;145-173.
154. Schauenstein K., Hayari Y. Avian lymphokines. Dev. Comp. Immunol. 7:1982;767-768.
155. Krömer G., Schauenstein K., Wick G. Avian lymphokines: an improved method for chicken IL-2 production and assay. A con A-erythrocyte complex induces higher T cell proliferation IL-2 production than does free mitogen. J. Immunol. Methods. 73:1984;273-281.
156. Vainio O., Ratcliffe M.J.H., Leerson T. Chicken T-cell growth factor: use in the generation of a long-term cultured T-cell line and biochemical characterization. Scand. J. Immunol. 23:1986;135-142.
157. Myers T.J., Lillehoj H.S., Fetterer R.H. Partial purification and characterisation of chicken interleukin-2. Vet. Immunol. Immunopathol. 34:1992;97-114.
158. Gillis S., Ferm M.M., Smith K.A. T cell growth factor: parameters of production and a quantitative mircoassay for activity. J. Immunol. 120:1978;2027-2032.
159. Corbel C., Thomas J.L. Establishment of an IL-2 dependent, antigen nonspecific chicken T-cell line. Dev. Comp. Immunol. 14:1990;439-446.
160. Kaplan M.H., Dhai A., Brown T.R., Sundick R.S. Marek's disease virus transformed cell lines respond to lymphokines. Vet. Immunol. Immunopathol. 34:1992;63-79.
161. Sundick R.S., Gill-Dixon C. A cloned chicken lymphokine homologous to both mammalian IL-2 and IL-15. J. Immunol. 159:1997;720-725.
162. Anderson D.M., Jonson L., Glaccum M.B., Copel N.G., Gilbert D.J., Jenkins N.A., et al. Chromosomal assignment and genomic structure of IL-15. Genomics. 25:1995;701-706.
163. Tagaya Y., Bamford R., DeFilippis A.P., Waldmann T.A. IL-15: a pleiotropic cytokine with diverse receptor/signal pathways whose expression is controlled at multiple levels. Immunity. 4:1996;329-336.
164. Bamford R.N., Grant A.J., Burton J.D., Peters C., Kurys G., Goldman C.K., et al. The interleukin (IL) 2 receptor beta chain is shared by IL-2 and a cytokine, provisionally designated IL-T, that stimulates T-cell proliferation and the induction of lymphokine-activated killer cells. Proc. Natl. Acad. Sci. USA. 91:1994;4940-4944.
165. Hala K., Schauenstein K., Neu N., Krömer G., Wolf H., Beck G., et al. A monoclonal antibody reacting with a membrane determinant on activated chicken T lymphocytes. Eur. J. Immunol. 16:1986;1331-1336.
166. Schauenstein K., Krömer G., Hala K., Bock G., Wick G. Chicken activated T lymphocyte antigen (CATLA) recognized by the monoclonal antibody INN-CH16 represents the IL-2 receptor. Dev. Comp. Immunol. 12:1988;823-831.
167. Lee T.-H., Tempelis C.H. Possible 110 kDa receptor for interleukin 2 in the chicken. Dev. Comp. Immunol. 16:1992;463-472.
168. Martin D.E., Glick B. Physiochemical characterization of lymphocyte inhibitory factor (LyIF) isolated from avian B and T cells. Cell. Immunol. 79:1983;383-388.
169. Joshi P., Glick B. Characterization of lymphocyte inhibitory factor from avian bursal and thymic lymphocytes and a chemotactic factor from thymic lymphocytes. Poultry Sci. 69:1990;249-258.
170. Joshi P., Glick B. The role of avian macrophages in the production of avian lymphokines. Dev. Comp. Immunol. 90:1990;319-325.
171. Landolfo S., Herberman B., Holden M.T. Macrophage lymphocyte interaction in MIF production. J. Immunol. 118:1977;1244-1248.
172. Rath N.C., Huff W.E., Bayyari G.R., Balog J.M. Identification of transformation growth factor-β and interleukin-6 in chicken ascites fluid. Avian Diseases. 39:1995;382-389.
173. Dodge W.H., Moscovici C. Colony formation by normal chick hematopoietic cells and leukaemic myeloblasts. J. Cell. Physiol. 30:1973;371-386.
174. Sharma S., Dodge W.H. Induction of colony-stimulating factor from quiescent fibroblasts by avian macrophages and monocytic leukemic cells. Leuk. Res. 9:1985;1507-1510.
175. Nicolas-Bolnet C., Qureshi M.A., Cieszynski J.A., Taylor R.L. Avian hematopoiesis in response to avian cytokines. Poultry Sci. 74:1995;1970-1974.
176. Klasing K.C. Avian inflammatory response: mediation by macrophages. Poultry Sci. 70:1991;1176-1186.
177. Siatskas C., McWaters P.G., Digby M., Lowenthal J.W., Boyd R.L. In vitro characterization of a novel avian haemopoietic growth factor derived from stromal cells. Dev. Comp. Immnunol. 20:1996;139-156.
178. Obranovich T.D., Boyd R.L. A bursal stromal derived cytokine induces proliferation of MHC class II bearing cells. Dev. Comp. Immnunol. 20:1996;61-75.
179. Silva R.F., Dodge W.H., Moscovici C. The role of humoral factors in the regression of leukemia in chickens as measured by in vitro colony formation. J. Cell. Physiol. 83:1973;187-192.
180. Bryant D., Smith R., Sharma S., Dodge W.H. Some circulating factors which influence granulocyte-monocyte production in the chick with myeloblastic leukemia. Cancer. Res. 40:1980;4031-4036.
181. Dodge W.H., Love S.H., Bryant D.L., Mitchell R.H. Properties of colony-stimulating and inhibiting activities of chicken serum. Exp. Hematol. 8:1980;395-403.
182. Bryant D.L., Dodge W.H. Studies on the circulating, colony-stimulatory activities in normal chicks and in chicks with myeloblastic leukemia. Exp. Hematol. 9:1981;457-467.
183. Bryant D.L., Whitaker J.M., Gruber K.A., Dodge W.H. Characterization of an inhibitor of granulocyte/monocyte colony formation in leukemic chicken plasma. Exp. Hematol. 9:1981;479-488.
184. Bryant D.L., Smith R.E., Dodge W.H. Levels of colony-stimulating
185. Byrnes S., Eaton R., Kogut M. In vitro interleukin-1 and tumor necrosis factor-alpha production by macrophages from chickens infected with either Eimeria maxima or Eimeria tenella. Int. J. Parasitol. 23:1993;639-645.
186. Zhang S, Lillehoj H.S., Ruff M.D. Chicken tumor necrosis-like factor. I. In vitro production by macrophages stimulated with Eimeria tenella or bacterial ploysaccharide. Poultry Sci. 74:1995;1304-1310.
187. Zhang S, Lillehoj H.S., Ruff M.D. In vivo role of tumor necrosis-like factor in Eimeria tenella infection. Avian Dis. 39:1995;859-866.
188. Yang Z., Petitte J.N. Use of avian cytokines in mammalian embryonic stem cell culture. Poultry Sci. 73:1994;965-974.
189. Samarut J., Nigon V. In vitro development of chicken erythropoietin-sensitive cells. Exp. Cell. Res. 100:1976;245-248.
190. Vainio O., Imhof B.A. The immunology and developmental biology of the chicken. Immunol. Today. 16:1995;365-370.
191. Beug H., Metz T., Mullner E.W., Hayman M.J. Self-renewal and differentiation in primary avian hematopoietic cells: an alternative to mammalian in vitro models. Wolff L., Perkins A.S. Molecular aspects of myeloid stem cell development. 1996;29-39 Springer, Berlin.
192. Nicolas-Bolnet C., Johnson P.A., Kemper A.E., Ricks C., Petitte J.N. Synergistic action of two sources of avian growth factors on proliferative differentiation of chick embryonic hematopoietic cells. Poultry Sci. 74:1995;1102-1116.
193. Johnson P.A., Liu H., O'Connell T., Phelps P., Bland M., Tyczkowski J., et al. Applications in in ovo technology. Poultry Sci. 76:1997;165-178.
194. Klasing K. Avian leukocytic cytokines. Poultry Sci. 73:1994;1035-1043.
195. Petrenko O., Ischenko I., Enrietto P.J. Isolation of a cDNA encoding a novel chicken chemokine homologous to mammalian macrophage inflammatory protein-1β Gene. 160:1995;305-306.
196. Barger B.O., Pace J.L., Inman F.P., Ragland W.L. Purification and partial characterization of an avian thymic hormone. Thymus. 17:1991;181-197.
197. Audhya T., Kroon D., Heavner G., Viamontes G., Goldstein G. Tripeptide structure of bursin, a selective B cell differentiating hormone of the bursa of Fabricius. Science. 231:1986;997-999.
198. Armani D.L., Mauzy-Melitz D., Mosesson M.W. Effect of hepatocyte stimulating factor and glycocorticoids on plasma fibronectin levels. J. Biochem. 238:1986;365-371.
199. Marsh J.A. The humoral activity of the avian thymic microenvironment. Poultry Sci. 72:1993;1294-1300.
200. Choi K.D., Lillehoj H.S., Song K.D., Han J.Y. Molecular and functional characterisation of chicken IL-15. Dev. Comp. Immunol. 23:1999;165-177.