用户名: 密码: 验证码:
The development and maintenance of the mononuclear phagocyte system of the chick is controlled by signals from the macrophage colony-stimulating factor receptor
详细信息    查看全文
  • 作者:Valerie Garceau (1)
    Adam Balic (1)
    Carla Garcia-Morales (1)
    Kristin A Sauter (1)
    Mike J McGrew (1)
    Jacqueline Smith (1)
    Lonneke Vervelde (1)
    Adrian Sherman (1)
    Troy E Fuller (2)
    Theodore Oliphant (2)
    John A Shelley (2)
    Raksha Tiwari (2)
    Thomas L Wilson (2)
    Cosmin Chintoan-Uta (1)
    Dave W Burt (1)
    Mark P Stevens (1)
    Helen M Sang (1)
    David A Hume (1)

    1. The Roslin Institute and Royal (Dick) School of Veterinary Studies
    ; The University of Edinburgh ; Easter Bush ; Midlothian ; EH25 9RG ; UK
    2. Zoetis
    ; 7000 Portage Road ; Kalamazoo ; MI ; 49001 ; USA
  • 关键词:Chicken ; CSF1 ; Hematopoiesis ; Macrophage ; Transgenic
  • 刊名:BMC Biology
  • 出版年:2015
  • 出版时间:December 2015
  • 年:2015
  • 卷:13
  • 期:1
  • 全文大小:3,874 KB
  • 参考文献:1. Hume, DA (2006) The mononuclear phagocyte system. Curr Opin Immunol. 18: pp. 49-53 CrossRef
    2. Gentek, R, Molawi, K, Sieweke, MH (2014) Tissue macrophage identity and self-renewal. Immunol Rev. 262: pp. 56-73 CrossRef
    3. Jenkins, SJ, Hume, DA (2014) Homeostasis in the mononuclear phagocyte system. Trends Immunol. 35: pp. 358-367 CrossRef
    4. Cuadros, MA, Martin, C, Coltey, P, Almendros, A, Navascues, J (1993) First appearance, distribution, and origin of macrophages in the early development of the avian central nervous system. J Comp Neurol. 330: pp. 113-129 CrossRef
    5. Cuadros, MA, Coltey, P, Carmen Nieto, M, Martin, C (1992) Demonstration of a phagocytic cell system belonging to the hemopoietic lineage and originating from the yolk sac in the early avian embryo. Development. 115: pp. 157-168
    6. Lichanska, AM, Browne, CM, Henkel, GW, Murphy, KM, Ostrowski, MC, McKercher, SR (1999) Differentiation of the mononuclear phagocyte system during mouse embryogenesis: the role of transcription factor PU.1. Blood. 94: pp. 127-138
    7. Lichanska, AM, Hume, DA (2000) Origins and functions of phagocytes in the embryo. Exp Hematol. 28: pp. 601-611 CrossRef
    8. Naito, M, Yamamura, F, Nishikawa, S, Takahashi, K (1989) Development, differentiation, and maturation of fetal mouse yolk sac macrophages in cultures. J Leukoc Biol. 46: pp. 1-10
    9. Hume, DA, MacDonald, KP (2012) Therapeutic applications of macrophage colony-stimulating factor-1 (CSF-1) and antagonists of CSF-1 receptor (CSF-1R) signaling. Blood. 119: pp. 1810-1820 CrossRef
    10. Nakamichi, Y, Udagawa, N, Takahashi, N (2013) IL-34 and CSF-1: similarities and differences. J Bone Miner Metab. 31: pp. 486-495 CrossRef
    11. Garceau, V, Smith, J, Paton, IR, Davey, M, Fares, MA, Sester, DP (2010) Pivotal advance: Avian colony-stimulating factor 1 (CSF-1), interleukin-34 (IL-34), and CSF-1 receptor genes and gene products. J Leukoc Biol. 87: pp. 753-764 CrossRef
    12. Sasmono, RT, Oceandy, D, Pollard, JW, Tong, W, Pavli, P, Wainwright, BJ (2003) A macrophage colony-stimulating factor receptor-green fluorescent protein transgene is expressed throughout the mononuclear phagocyte system of the mouse. Blood. 101: pp. 1155-1163 CrossRef
    13. Schulz, C, Gomez Perdiguero, E, Chorro, L, Szabo-Rogers, H, Cagnard, N, Kierdorf, K (2012) A lineage of myeloid cells independent of Myb and hematopoietic stem cells. Science. 336: pp. 86-90 CrossRef
    14. Dai, X-M, Ryan, GR, Hapel, AJ, Dominguez, MG, Russell, RG, Kapp, S (2002) Targeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects. Blood. 99: pp. 111-120 CrossRef
    15. Erblich, B, Zhu, L, Etgen, AM, Dobrenis, K, Pollard, JW (2011) Absence of colony stimulation factor-1 receptor results in loss of microglia, disrupted brain development and olfactory deficits. PLOS One. 6: pp. e26317 CrossRef
    16. Ginhoux, F, Greter, M, Leboeuf, M, Nandi, S, See, P, Gokhan, S (2010) Fate mapping analysis reveals that adult microglia derive from primitive macrophages. Science. 330: pp. 841-845 CrossRef
    17. Hashimoto, D, Chow, A, Noizat, C, Teo, P, Beasley, MB, Leboeuf, M (2013) Tissue-resident macrophages self-maintain locally throughout adult life with minimal contribution from circulating monocytes. Immunity. 38: pp. 792-804 CrossRef
    18. McGrew, MJ, Sherman, A, Lillico, SG, Ellard, FM, Radcliffe, PA, Gilhooley, HJ (2008) Localised axial progenitor cell populations in the avian tail bud are not committed to a posterior Hox identity. Development. 135: pp. 2289-2299 CrossRef
    19. Zhao, D, McBride, D, Nandi, S, McQueen, HA, McGrew, MJ, Hocking, PM (2010) Somatic sex identity is cell autonomous in the chicken. Nature. 464: pp. 237-242 CrossRef
    20. Garcia-Morales, C, Rothwell, L, Moffat, L, Garceau, V, Balic, A, Sang, HM (2014) Production and characterisation of a monoclonal antibody that recognises the chicken CSF1 receptor and confirms that expression is restricted to macrophage-lineage cells. Dev Comp Immunol. 42: pp. 278-285 CrossRef
    21. Balic, A, Garcia-Morales, C, Vervelde, L, Gilhooley, H, Sherman, A, Garceau, V (2014) Visualisation of the avian mononuclear phagocyte system using novel transgenic reporter genes based upon conserved elements of the CSF1R locus. Development. 141: pp. 3255-3265 CrossRef
    22. Freeman, TC, Ivens, A, Baillie, JK, Beraldi, D, Barnett, MW, Dorward, D (2012) A gene expression atlas of the domestic pig. BMC Biol. 10: pp. 90 CrossRef
    23. Hume, DA, Summers, KM, Raza, S, Baillie, JK, Freeman, TC (2010) Functional clustering and lineage markers: insights into cellular differentiation and gene function from large-scale microarray studies of purified primary cell populations. Genomics. 95: pp. 328-338 CrossRef
    24. Mabbott, NA, Kenneth Baillie, J, Hume, DA, Freeman, TC (2010) Meta-analysis of lineage-specific gene expression signatures in mouse leukocyte populations. Immunobiology. 215: pp. 724-736 CrossRef
    25. Jaffredo, T, Gautier, R, Eichmann, A, Dieterlen-Lievre, F (1998) Intraaortic hemopoietic cells are derived from endothelial cells during ontogeny. Development. 125: pp. 4575-4583
    26. Saynajakangas, R, Uchida, T, Vainio, O (2009) Differential gene expression in CD45 cells at para-aortic foci stage of chicken haematopoiesis. Scand J Immunol. 70: pp. 288-294 CrossRef
    27. Macdonald, J, Taylor, L, Sherman, A, Kawakami, K, Takahashi, Y, Sang, HM (2012) Efficient genetic modification and germ-line transmission of primordial germ cells using piggyBac and Tol2 transposons. Proc Natl Acad Sci U S A. 109: pp. E1466-E1472 CrossRef
    28. Wong, GK, Cavey, MJ (1993) Development of the liver in the chicken embryo. II. Erythropoietic and granulopoietic cells. Anat Rec 235: pp. 131-143 CrossRef
    29. Douarin, NM, Dieterlen-Lievre, F, Oliver, PD (1984) Ontogeny of primary lymphoid organs and lymphoid stem cells. Am J Anat. 170: pp. 261-299 CrossRef
    30. Houssaint, E, Lassila, O, Vainio, O (1989) Bu-1 antigen expression as a marker for B cell precursors in chicken embryos. Eur J Immunol. 19: pp. 239-243 CrossRef
    31. Gow, DJ, Sauter, KA, Pridans, C, Moffat, L, Sehgal, A, Stutchfield, BM (2014) Characterisation of a novel Fc conjugate of macrophage colony-stimulating factor. Mol Ther. 22: pp. 1580-1592
    32. Ulich, TR, Castillo, J, Watson, LR, Yin, SM, Garnick, MB (1990) In vivo hematologic effects of recombinant human macrophage colony-stimulating factor. Blood. 75: pp. 846-850
    33. Jeurissen, SH, Janse, EM (1989) Distribution and function of non-lymphoid cells in liver and spleen of embryonic and adult chickens. Prog Clin Biol Res. 307: pp. 149-157
    34. Alikhan, MA, Jones, CV, Williams, TM, Beckhouse, AG, Fletcher, AL, Kett, MM (2011) Colony-stimulating factor-1 promotes kidney growth and repair via alteration of macrophage responses. Am J Pathol. 179: pp. 1243-1256 CrossRef
    35. Hume, DA, Pavli, P, Donahue, RE, Fidler, IJ (1988) The effect of human recombinant macrophage colony-stimulating factor (CSF-1) on the murine mononuclear phagocyte system in vivo. J Immunol. 141: pp. 3405-3409
    36. Felix, R, Hofstetter, W, Wetterwald, A, Cecchini, MG, Fleisch, H (1994) Role of colony-stimulating factor-1 in bone metabolism. J Cell Biochem. 55: pp. 340-349 CrossRef
    37. Alexander, KA, Chang, MK, Maylin, ER, Kohler, T, Muller, R, Wu, AC (2011) Osteal macrophages promote in vivo intramembranous bone healing in a mouse tibial injury model. J Bone Miner Res. 26: pp. 1517-1532 CrossRef
    38. Chang, MK, Raggatt, LJ, Alexander, KA, Kuliwaba, JS, Fazzalari, NL, Schroder, K (2008) Osteal tissue macrophages are intercalated throughout human and mouse bone lining tissues and regulate osteoblast function in vitro and in vivo. J Immunol. 181: pp. 1232-1244 CrossRef
    39. Epelman, S, Lavine, KJ, Randolph, GJ (2014) Origin and functions of tissue macrophages. Immunity. 41: pp. 21-35 CrossRef
    40. Hughes, S, Poh, TY, Bumstead, N, Kaiser, P (2007) Re-evaluation of the chicken MIP family of chemokines and their receptors suggests that CCL5 is the prototypic MIP family chemokine, and that different species have developed different repertoires of both the CC chemokines and their receptors. Dev Comp Immunol. 31: pp. 72-86 CrossRef
    41. Fife, MS, Howell, JS, Salmon, N, Hocking, PM, Diemen, PM, Jones, MA (2010) Genome-wide SNP analysis identifies major QTL for Salmonella colonization in the chicken. Anim Genet. 42: pp. 134-140 CrossRef
    42. Smith, J, Sadeyen, JR, Paton, IR, Hocking, PM, Salmon, N, Fife, M (2011) Systems analysis of immune responses in Marek鈥檚 disease virus-infected chickens identifies a gene involved in susceptibility and highlights a possible novel pathogenicity mechanism. J Virol. 85: pp. 11146-11158 CrossRef
    43. Hettinger, J, Richards, DM, Hansson, J, Barra, MM, Joschko, AC, Krijgsveld, J (2013) Origin of monocytes and macrophages in a committed progenitor. Nat Immunol. 14: pp. 821-830 CrossRef
    44. Breen, FN, Hume, DA, Weidemann, MJ (1991) Interactions among granulocyte-macrophage colony-stimulating factor, macrophage colony-stimulating factor, and IFN-gamma lead to enhanced proliferation of murine macrophage progenitor cells. J Immunol. 147: pp. 1542-1547
    45. Lavin, Y, Merad, M (2013) Macrophages: gatekeepers of tissue integrity. Cancer Immunol Res. 1: pp. 201-209 CrossRef
    46. Epelman, S, Lavine, KJ, Beaudin, AE, Sojka, DK, Carrero, JA, Calderon, B (2014) Embryonic and adult-derived resident cardiac macrophages are maintained through distinct mechanisms at steady state and during inflammation. Immunity. 40: pp. 91-104 CrossRef
    47. Jenkins, SJ, Ruckerl, D, Thomas, GD, Hewitson, JP, Duncan, S, Brombacher, F (2013) IL-4 directly signals tissue resident macrophages to proliferate beyond homeostatic levels controlled by CSF-1. J Exp Med. 210: pp. 2477-2491 CrossRef
    48. Karasuyama, H (1988) Establishment of mouse cell lines which constitutively secrete large quantities of interleukin 2, 3, 4 or 5, using high-copy cDNA expression vectors. Tanpakushitsu Kakusan Koso 33: pp. 2527-2532
    49. Kapetanovic, R, Fairbairn, L, Beraldi, D, Sester, DP, Archibald, AL, Tuggle, CK (2012) Pig bone marrow-derived macrophages resemble human macrophages in their response to bacterial lipopolysaccharide. J Immunol. 188: pp. 3382-3394 CrossRef
    50. Hamburger V, Hamilton HL. A series of normal stages in the development of the chick embryo. Dev Dyn. 1992. 1951;195:231鈥?2.
    51. Nieto, MA, Patel, K, Wilkinson, DG (1996) In situ hybridization analysis of chick embryos in whole mount and tissue sections. Methods Cell Biol. 51: pp. 219-235 CrossRef
  • 刊物主题:Life Sciences, general;
  • 出版者:BioMed Central
  • ISSN:1741-7007
文摘
Background Macrophages have many functions in development and homeostasis as well as innate immunity. Recent studies in mammals suggest that cells arising in the yolk sac give rise to self-renewing macrophage populations that persist in adult tissues. Macrophage proliferation and differentiation is controlled by macrophage colony-stimulating factor (CSF1) and interleukin 34 (IL34), both agonists of the CSF1 receptor (CSF1R). In the current manuscript we describe the origin, function and regulation of macrophages, and the role of CSF1R signaling during embryonic development, using the chick as a model. Results Based upon RNA-sequencing comparison to bone marrow-derived macrophages grown in CSF1, we show that embryonic macrophages contribute around 2% of the total embryo RNA in day 7 chick embryos, and have similar gene expression profiles to bone marrow-derived macrophages. To explore the origins of embryonic and adult macrophages, we injected Hamburger-Hamilton stage 16 to 17 chick embryos with either yolk sac-derived blood cells, or bone marrow cells from EGFP+ donors. In both cases, the transferred cells gave rise to large numbers of EGFP+ tissue macrophages in the embryo. In the case of the yolk sac, these cells were not retained in hatched birds. Conversely, bone marrow EGFP+ cells gave rise to tissue macrophages in all organs of adult birds, and regenerated CSF1-responsive marrow macrophage progenitors. Surprisingly, they did not contribute to any other hematopoietic lineage. To explore the role of CSF1 further, we injected embryonic or hatchling CSF1R-reporter transgenic birds with a novel chicken CSF1-Fc conjugate. In both cases, the treatment produced a large increase in macrophage numbers in all tissues examined. There were no apparent adverse effects of chicken CSF1-Fc on embryonic or post-hatch development, but there was an unexpected increase in bone density in the treated hatchlings. Conclusions The data indicate that the yolk sac is not the major source of macrophages in adult birds, and that there is a macrophage-restricted, self-renewing progenitor cell in bone marrow. CSF1R is demonstrated to be limiting for macrophage development during development in ovo and post-hatch. The chicken provides a novel and tractable model to study the development of the mononuclear phagocyte system and CSF1R signaling.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700