Developmental derivation of embryonic and adult macrophages

Current Opinion in Hematology

Volumn 7, Issue 1, 2000, Pages 3-8

  Shepard, Jennifer L ^a   Zon, Leonard I ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE MARROW CELL; CELL DIFFERENTIATION; CELL FUNCTION; CELL LINEAGE; CELL MATURATION; EMBRYO; EVOLUTION; GENETIC CONSERVATION; HEMATOPOIESIS; HUMAN; MACROPHAGE; MONOCYTE; NONHUMAN; PRIORITY JOURNAL; REVIEW; STEM CELL;

AGE FACTORS; ANIMALS; CELL LINEAGE; EMBRYO; FEMALE; HUMANS; MACROPHAGES; MICE;

EID: 0033988290     PISSN: 10656251     EISSN: None     Source Type: Journal    
DOI: 10.1097/00062752-200001000-00002     Document Type: Review

References (46)

1. 1 Sanchez M, Holmes A, Miles C, Dzierzak E: Characterization of the first definitive hematopoietic stem cells in the AGM and liver of the mouse embryo. Immunity 1996, 5:513-525.
2. 2 Metcalf D, Nicola NA: The hemopoietic colony-stimulating factors. New York: Cambridge University Press; 1995.
3. 3 Metcalf D, Burgess AW: Clonal analysis of progenitor cell commitment to granulocyte or macrophage production. J Cell Physiol 1982, 111:275-283.
4. 4 Goud TJLM, Chotte C, Van Furth R: Identification and characterization of the monoblast in mononuclear phagocyte colonies grown in vitro. J Exp Med 1975, 142:1180-1199.
5. 5 Van Furth R, Cohn ZA: The origin and kinetics of mononuclear phagocytes. J Exp Med 1968, 128:415-433.
6. 6 Goud TJLM, Van Furth R: Proliferative characteristics of monoblasts grown in vitro. J Exp Med 1975, 142:1200-1217.
7. 7 Van Furth R, Diesselhoff-den Dulk MMC: The kinetics of promonocytes and monocytes in the bone marrow. J Exp Med 1970, 132:813-828.
8. 8 Van Furth R, Cohn ZA, Hirsch JG, Humphrey JH, Spector WG, Langevoort HL: The mononuclear phagocyte system: a new classification of macrophages, monocytes and their precursor cells. Bull World Health Org 1972, 46:845-852.
9. 9 Aschoff L: Das Reticulo-endotheliale System. Innere Med Kinderheilkd 1924, 26:1-118.
10. 10 Leenen PJM, Campbell PA: Heterogeneity of mononuclear phagocytes: in interpretive review. In Blood Cell Biochemistry-Macrophages and Related Cells. Edited by Horton MA. New York: Plenum Press; 1993:29-86.
11. 11 Ginsel LA: Origin of macrophages. In Blood Cell Biochemistry-Macrophages and Related Cells. Edited by Horton MA. New York: Plenum Press; 1993:87-114.
12. 12 Dantschakoff W: Untersuchungen über die Entwicklung des Blutes und des Bindesgewebes bei den Vögeln: I.: die erste Entstehung der Blutbildenes Organ. Anat Hefte Wiesb 1908, 37:471-479.
13. 13 Moore MAS, 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 1970, 18:279-296.
14. 14 Cline MJ, Moore MAS: Embryonic origin of the mouse macrophage. Blood 1972, 39:842-849.
15. 15 Takahashi K, Yamamura F, Naito M: Differentiation, maturation, and proliferation of macrophages in the mouse yolk sac: a light-microscopic, enzyme-cytochemical, immunohistochemical, and ultrastructural study. J Leuk Biol 1989, 45:87-96.
16. 16 Takahashi K, Naito M: Development, differentiation and proliferation of macrophages in the rat yolk sac. Tissue Cell 1993, 25:351-362.
17. 17 Takahashi K, Naito M, Takeya M: Development and heterogeneity of macrophages and their related cells through their differentiation pathways. Pathol Int 1996, 46:473-485.
18. 18 Cuadros MA, Coltey P, Nieto MC, Martin C: Demonstration of a phagocytic cell system belonging to the hemopoietic lineage and originating from the yolk sac in the early avian embryo. Development 1992, 115:157-168.
19. 19 Dieterlen-Lierve F: Blood in chimeras. In Chimeras in Developmental Biology. Edited by Le Douarin NM, McLaren A. London: Academic Press; 1984:133-163.
20. 20 Cuadros MA, Martin C, Coltey P, Almedros A, Nacascues J: First appearance, distribution, and origin of macrophages in the early development of the avian central nervous system. J Comp Neur 1993, 330:113-129.
21. 21 Detrich HW 3rd, Kieran MW, Chan FY, Barone LM, Yee K, Rundstadler JA, et al.: Intraembryonic haematopoietic cell migration during vertebrate development. Proc Nat Acad Sci, USA 1995, 92:10713-10717.
22. 22 Amatruda JF, Zon LI: Dissecting hematopoiesis and disease using the zebrafish. Dev Biol 1999, 216:1-15. This article reviews the zebrafish hematopoietic program and discusses recent advances in zebrafish models of human disease.
23. 23 Hermbomel P, Thisse B, Thisse C: Ontogeny and behaviour of early macrophages in the zebrafish embryo. Development 1999, 126: 3735-3745. The authors of this article demonstrate that macrophages appear early on in zebrafish development and originate separately from monocytic cells. These macrophages are also shown to have phagocytic capability to eradicate embryonic bacterial infections.
24. 24 Thompson MA, Ransom DG, Pratt SJ, MacLennan H, Kieran MW, Detrich HW, et al.: The cloche and spadetail genes differentially affect hematopoiesis and vasculogenesis. Dev Biol 1998, 197:248-269.
25. 25 Ohinata H, Tochinai S, Katagiri C: Ontogeny and tissue distribution of leukocyte-common antigen bearing cells during early development of Xenopus laevis. Development 1989, 107:445-452.
26. 26 Miyanaga Y, Shiurba R, Nagata S, Pfeiffer CJ, Asashima M: Induction of blood cells in Xenopus embryo explants. Dev Genes Evol 1998, 207:417-26.
27. 27 Ohinata H, Tochinai S, Katagiri C: Occurrence of nonlymphoid leukocytes that are not derived from blood islands in Xenopus laevis larvae. Dev Biol 1990, 141:123-129.
28. 28 Hoffman JA, Zachary D, Hoffman D, Brehelin M, Porte A: Postembryonic development land differentiation: hemopoietic tissues and their function in some insects. In Insect Hemocytes. Edited by AP Gupta. Cambridge, UK: Cambridge University Press; 1979.
29. 29 Tepass U, Fessler LI, Aziz A, Hartenstein V: Embryonic origin of hemocytes and their relationship to cell death in Drosophila. Development 1994, 120:1829-1837.
30. 30 Franc NC, Dimarcq J, Lagueux M, Hoffmann J, Ezekowitz RAB: Croquemort, a novel Drosophila hemocyte/macrophage receptor that recognizes apoptotic cells. Immunity 1996, 4:431-443.
31. 31 Ellis RE, Yuan J, Horvitz HR: Mechanisms and functions of cell death. Annu Rev Cell Biol 1991, 7:663-698.
32. 32 Luciani M, Chimini G: The ATP binding cassette transporter ABC1 is required for the engulfment of corpses generated by apoptotic cell death. EMBO J 1996, 15:226-235.
33. 33 Hopkinson-Woolley J, Hughes D, Gordon S, Martin P: Macrophage recruitment during limb development and wound healing in the embryonic and foetal mouse. J Cell Sci 1994, 107:1159-1167.
34. 34 Huber MC, Graf R, Sippel AE, Bonifer C: Dynamic changes in the chromatin of the chicken lysozyme gene domain during differentiation of multipotent progenitors to macrophages. DNA Cell Biol 1995, 14:397-402.
35. 35 Faust N, Huber MC, Sippel AE, Bonifer C: Different macrophage populations develop from embryonic/fetal and adult hematopoietic tissues. Exp Hemat 1997, 25:432-444.
36. 36 Sherr CJ, Rettenmier CW, Sacca R, Roussel MF, Look AT, Stanley ER: The c-fms proto-oncogene product is related to the receptor for the mononuclear phagocyte growth factor, CSF-1. Cell 1985, 41:665-676.
37. 37 Hume D, Monkley S, Wainwright B: Detection of c-fms proto-oncogene in early mouse embryos by whole mount in situ hybridization indicates roles for macrophages in tissue remodelling. Br J Haematol 1995, 90:939-942.
38. 38 Yue X, Favot P, Dunn T, Cassady A, Hume D: Expressin of mRNA encoding the macrophage colony-stimulating factor receptor (c-fms) is controlled by a constitutive promoter and tissue-specific transcription elongation. Mol Cell Biol 1993, 13:391.
39. 39 Klemsz MJ, McKercher SR, Celada A, Van Beveren C, Maki RA: The macrophage and B cell specific transcription factor PU.1 is related to the ets oncogene. Cell 1990, 61: 113-124.
40. 40 Moreau-Gachelin F, Ray D, Tambourin P, Tavitian A, Klemsz ML, McKercher SR, et al.: The PU.1 transcription factor is the product of the putative oncogene Spi-1. Cell 1990,61:1165-1166.
41. 41 Valledor AF, Borras FE, Cullell-Young M, Celada A: Transcription factors that regulate monocyte/macrophage differentiation. J Leukocyte Biol 1998, 63:405-417.
42. 42 Scott EW, Simon MC, Anastasi J, Singh H: Requirement of transcription factor PU.1 in the development of multiple hematopoietic lineages. Science 1994, 265:1573-1577.
43. 43 McKercher S, Torbett B, Anderson K, Henkel G, Vestal D, Baribault H, et al.: Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities. EMBO J 1996, 15:5647.
44. 44 Olson MC, Scott EW, Hack AA, Su GH, Tene DG, Singh H, Simon MC: PU.1 is not essential for early myeloid gene expression but is required for terminal myeloid differentiation. Immunity 1995, 3:703-714.
45. 45 Anderson KL, Smith KA, Conners K, McKercher SR, Maki RA, Torbett BE: Myeloid development is selectively disrupted in PU.1 null mice. Blood 1998,91:3702-3710. This study shows that the PU.1 disruption in mice causes a loss of monocyte/macrophages and that PU.1 null hematopoietic cells fail to respond to G-CSF or GM-CSF.
46. 46 Lichanska AM, Browne CM, Henkel GW, Murphy KM, Ostrowski MC, McKercher SR, et al.: Differentiation of the mononuclear phagocyte system during mouse embryogenesis: the role of transcription factor PU.1. Blood 1999,94:127-138. This intriguing article supports previous data that PU.1 null mice have a lack of monocyte-derived macrophages, but suggests that yolk sac-derived macrophages are retained. This affirms the theory that fetal phagocytes are separate from macrophages arising during definitive hematopoiesis.