Development and heterogeneity of macrophages and their related cells through their differentiation pathways

Pathology International

Volumn 46, Issue 7, 1996, Pages 473-485

  Takahashi, Kiyoshi ^a   Naito, Makoto ^b   Takeya, Motohiro ^a  

^a KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

^b NIIGATA UNIVERSITY   (Japan)

Author keywords

colony stimulating factors; dendritic cells; macrophage subpopulations; ontogeny; osteopetrotic mouse

Indexed keywords

COLONY STIMULATING FACTOR 1; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; GROWTH FACTOR;

BONE MARROW CELL; CELL DIFFERENTIATION; CELL MATURATION; HEMATOPOIESIS; HEMATOPOIETIC STEM CELL; MACROPHAGE; MONOCYTE; NONHUMAN; ONTOGENY; PRIORITY JOURNAL; REVIEW;

EID: 0029781035     PISSN: 13205463     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1440-1827.1996.tb03641.x     Document Type: Review

References (133)

1. Metchnikoff E. Lecons sur la Pathologie Comparee de L'inflammation. Masson, Paris. 1892.
2. Aschoff L. Das reticuloendotheliale system. Erg. Inn. Med. Kinderheilk. 1924; 26, 1-118.
3. Langevoort HL, Cohn ZA, Hirsh JG et al. The nomenclature of mononuclear phagocytic cells: Proposal for a new classification. In: van Furth R, ed. Mononuclear Phagocytes, Blackwell Science, Oxford, 1970; 1-6.
4. van Furth R, Cohn ZA, Hirsh JG et al. The mononuclear phagocyte system: A new classification of macrophages, monocytes, and their precursor cells. Bull. WHO. 1972; 46: 845-852.
5. van Furth R, Langevoort HL, Schaberg A. Mononuclear phagocytes in human pathology - proposal for an approach to improved classification. In: van Furth R, ed. Mononuclear Phagocytes in Immunity, Infection and Pathology, Blackwell Science, Oxford, 1975; 1-15.
6. van Furth R. Cells of the mononuclear phagocyte system. Nomenclature in terms of sites and conditions. In: van Furth R, ed. Mononuclear Phagocytes, Functional aspects Part 1, Martinus Nijhoff Publishers, The Hague, 1980; 1-30.
7. van Furth R. Development of mononuclear phagocytes. In: Foerster O, Landy M, eds. Heterogeneity of Mononuclear Phagocytes, Academic Press Inc., London, 1981, 3-10.
8. van Furth R. Origin and turnover of monocytes and macrophages. In: Iverson OH, ed. Cell Kinetics of the Inflammatory Reaction, Springer-Verlag, Berlin-Heidelberg, 1989; 125-150.
9. Kojima M, Macrophages, reticuloendothelial system and mononuclear phagocyte system. Rec. Adv. RES Res. 1976; 16: 1-25.
10. Carr I, Daems WT, eds. The Reticuloendothelial System: A Comprehensive Treatise. Plenum Press, New York, 1980.
11. Volkman A, ed. Mononuclear Phagocyte Biology. Marcel Dekker, Inc., New York, 1984.
12. Morahan PS, Volkman A, Melnicoff M et al. Macrophage heterogeneity. In: Heppner GH, Fulton AM, eds. Macrophages and Cancer. CRC Press, Inc., Florida, 1988; 1-25.
13. Leenen PJM, Campbell PA. Heterogeneity of mononuclear phagocytes. An interpretive review. Blood Cell Biochem. 1993; 5: 29-85.
14. Daems WT, Brederro P. The fine structure and peroxidase activity of resident and exudate macrophages in the guinea pigs. In: DiLuzio NR, Flemming K, eds. The Reticuloendothelial System and Immune Phenomena. Plenum Press, New York, 1972; 19-31.
15. Daems WT, Brederoo R. Electron microscopical studies on the structure, phagocytic properties and peroxidase activity of resident and exudate peritoneal macrophages in guinea pigs. Z. Zellforsch. 1973; 144: 247-297.
16. Daems WT, Koerten HK, Soranzo MR. Differences between monocyte-derived and tissue macrophages. In: Reichard SM, Escobar MR, Friedman H, eds. The Reticuloendothelial System in Health and Disease, Functions and Characteristics. 1976; 27-40.
17. Daems WT, Roos D, van Berkel TJC et al. The subcellular distribution and biochemical properties of peroxidase in monocytes and macrophages. In: Dingle JT, Jacques PJ, eds. Lysosomes in Biology and Pathology, vol. 6. North-Holland Publishing Co., Amsterdam, 1979; 463-516.
18. Bodel PT, Nichols BA, Bainton DF. Appearance of peroxidase reactivity within the rough endoplasmic reticulum of blood monocytes after surface adherence. J. Exp. Med. 1977; 145: 264-274.
19. Bodel PT, Nichols BA, Bainton DF. Difference of peroxidase localization of rabbit peritoneal macrophages after surface adherence. Am. J. Pathol. 1978; 91: 107-117.
20. Beelen RHJ, van't Veer M, Fluitsma DM et al. Identification of different peroxidatic activity patterns in peritoneal macrophages in vivo and in vitro. J. Reticuloendothel. Soc. 1978; 24: 351-362.
21. Beelen RHJ, Fluitsma DM, van der Meer JWM et al. Development of different peroxidatic activity patterns in peritoneal macrophages in vivo and in vitro. J. Reticuloendothel. Soc. 1979; 25: 513-523.
22. Beelen RHJ, Fluitsma DM, van der Meer JWM et al. Development of exudate-resident macrophages, on the basis of the pattern of peroxidatic activity in vivo and in vitro. In: van Furth R. ed. Mononuclear Phagocytes, Functional aspects, Part 1. Martinus Nijhoff Publishers, The Hague, 1980; 87-112.
23. Bainton DF. Changes in peroxidase distribution within organelles of blood monocytes and peritoneal macrophages after surface adherence in vitro and in vivo. In: van Furth R, ed. Mononuclear Phagocytes, Functional aspects, Part 1, Martinus Nijhoff Publishers, The Hague, 1980; 61-86.
24. Naito M, Oka K, Miyazaki M et al. Ultrastructural and cytochemical changes of monocytes and macrophages in vivo and in vitro. Rec. Adv. RES Res. 1979; 18: 66-82.
25. Daems WT, van der Rhee HJ. Peroxidase and catalase in monocytes, macrophages, epithelioid cells and giant cells of the rat. In: van Furth R, ed. Mononuclear Phagocytes, Functional aspects, Part 1, Martinus Nijhoff Publishers, The Hague, 1980; 43-60.
26. Fahimi HD, Gray BA, Herzog VK. Cytochemical localization of catalase and peroxidase in sinusoidal cells of rat liver. Lab. Invest. 1976; 34: 192-201.
27. Deimann W. Endogenous peroxidase activity in mononuclear phagocytes. Prog. Histochem. Cytochem. 1984; 15: 1-56.
28. Shellitto J, Sniezek M, Warnock M. Acquisition of peroxidase activity by rat alveolar macrophages during pulmonary inflammation. Am. J. Pathol. 1987; 129: 567-577.
29. Schmekel R, Hornbland Y, Linden M et al. Myeloperoxidase in human lung lavage. II. Internalization of myeloperoxidase by alveolar macrophages. Inflammation 1990; 14: 455-461.
30. Ginsel LA, de Water R, van der Meer JWM et al. Heterogeneity of 5′-nucleotidase activity and wheat-germ agglutinin binding in mononuclear phagocytes. In: van Furth R, ed. Mononuclear Phagocytes, Characteristics, Physiology, and Function. Martinus Nijhoff Publishers, Dordrecht, 1985; 99-113.
31. Takeya M, Hsiao L, Takahashi K. A new monoclonal antibody, TRPM-3, binds specifically to certain rat macrophage populations: Immunohistochemical and immunoelectron microscopic analysis. J. Leukocyte Biol. 1987; 41: 187-195.
32. Dijkstra CD, Doepp EA, Joling P et al. The heterogeneity of mononuclear phagocytes in lymphoid organs: Distinct macrophage subpopulation in the rat recognized by monoclonal antibodies ED1, ED2, and ED3. Immunology 1985; 54: 589-599.
33. Beelen RHJ, Estermans IL, Doepp EA et al. ED1, ED2, and ED3 against rat macrophages: Expressions of recognized antigens in different stages of differentiation. Transplant Proc. 1987; 19: 3166-3170.
34. Wacker HH, Radzun HJ, Parwaresh MR. Ki-M2R, a new specific monoclonal antibody, discriminates tissue macrophages from reticulum cells and monocytes in vivo and in vitro. J. Leukocyte Biol. 1985; 38: 509-520.
35. Miyamura S, Naito M, Takeya M et al. Analysis of rat peritoneal macrophages with combined ultrastructural peroxidase cytochemistry and immunoelectron microscopy using anti-rat macrophage monoclonal antibodies. J. Clin. Electron Microsc. 1998; 21: 5-6.
36. Takahashi K, Naito M, Takeya M. The nature of resident macrophages. In: Kim SH, Kojima M, eds. Lymphoreticular Tissue and Diseases. Korea Medical Publishing Co., Seoul, 1989; 19-39.
37. Sakanashi H, Takeya M, Yoshimura T et al. Kinetics of macrophage subpopulations and expression of monocyte chemoattractant protein-1 (MCP-1) in bleomycin-induced lung injury of rats studied by a novel monoclonal antibody against rat MCP-1. J. Leukocyte Biol. 1994; 56: 741-750.
38. Yamashiro S, Takeya M, Nishi T et al. Tumor-associated monocyte chemoattractant protein-1 induced intratumoral infiltration of monocyte-derived macrophage subpopulation in transplantable rat tumor. Am. J. Pathol. 1994; 145: 86-867.
39. Kraal G, Janse M. Marginal metallophilic cells of the mouse spleen identified by a monoclonal antibody. Immunology 1986; 38: 665-669.
40. Kraal G, Janse M. Marginal metallophilic macrophages in the mouse spleen: Effects of neonatal injections of MOMA-1 antibody on the humoral immune response. Immunol. Lett. 1988; 17: 139-144.
41. van Rooijen N, Kors N, Kraal G. Macrophage subset repopulation in the spleen: Differential kinetics after liposome-mediated elimination. J. Leukocyte Biol. 1989; 45: 97-104.
42. Dijkstra CD, van Vliet E, Doepp EA et al. Marginal zone macrophages in the mouse spleen identified by a monoclonal antibody: Characterization of immuno- and enzyme-histochemical properties and functional capacities. Immunology 1985; 55: 23-30.
43. van Vielt E, Melis M, van Ewijk W. Marginal zone macrophages in the mouse spleen identified by a monoclonal antibody: Anatomical correlation with a B cell subpopulation. J. Histochem. Cytochem. 1985; 33: 40-44.
44. Hume DA, Robinson AP, Macpherson GG et al. The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80. J. Exp. Med. 1983; 158: 1522-1536.
45. Umeda S, Takahashi K, Shultz DL et al. Effects of macrophage colony stimulating factor (M-CSF) on macrophages and their related cell populations in osteopetrosis (op) mouse defective in production of functional M-CSF protein. Am. J. Pathol. 1996; 149 (in press).
46. Elomaa O, Kongas G, Sahlberg C et al. Cloning of a novel bacteria-binding receptor structurally related to scavenger receptors and expressed in a subset of macrophages. Cell 1995; 80: 603-609.
47. Humphry JH. Tolerogenic or immunogenic activity of hapten-conjugated polysaccharides correlated with cellular localization. Eur. J. Immunol. 1981; 11: 212-230.
48. Kraal G, Hart HT, Meelhuizen C et al. Marginal zone macrophages and their role in the immune response against T-independent type 2 antigens: Modulation of the cells with specific antibody. Eur. J. Immunol. 1989; 19: 675-680.
49. Classen E, Ott A, Boersma WJA et al. Marginal zone of the mouse spleen in autotransplants: Functional and histological observations in the response against thymus-independent type 2 antigen. Clin. Exp. Immunol. 1989; 77: 445-451.
50. van Rooijen N, Kors N. Effects of intracellular diphosphonates on cells of the mononuclear phagocyte system: In vivo effects of liposome-encapsulated diphosphonates on different macrophage subpopulations in the spleen. Calcif. Tissue Int. 1989; 45: 153-156.
51. van Rooijen N, Kors N, van der Endde M et al. Depletion and repopulation of macrophages in spleen and liver of rat after intravenous treatment with liposome-encapsulated dicholoromethylene diphosphonate. Cell Tissue Res. 1990; 260: 215-222.
52. Burkley PJ. Phenotypic subpopulations of macrophages and dendritic cells in human spleen. Scanning Microsc. 1991; 5: 147-158.
53. van Furth R, Diesselhoff-den Dulk MMC, Sluiter W et al. New perspectives on the kinetics of mononuclear phagocytes. In: van Furth R, ed. Mononuclear Phagocytes, Characteristics. Physiology and Function. Martinus Nijhoff Publishers, Dordrecht, 1998; 201-210.
54. van Furth R. Production and migration of monocytes and kinetics of macrophages. In: van Furth R, ed. Mononuclear Phagocytes: Biology of Monocytes and Macrophages. Kluwer Academic Publishers, Dordrecht, 1992; 2-12.
55. 2-dependent and independent immune suppressor cells by tumor-derived GM-CSF and M-CSF. J. Leukocyte Biol. 1993; 53: 86-92.
56. Honda Y, Takahashi K, Naito M et al. The role of macrophage colony-stimulating factor in the differentiation and proliferation of Kupffer cells in the liver of protein-derived mice. Lab. Invest. 1995; 72: 696-706.
57. Volkman A, Chang NC, Strausbauch PH et al. Differential effects of chronic monocyte depletion on macrophage populations. Lab. Invest. 1983; 49: 291-298.
58. Yamada M, Naito M, Takahashi K. Kupffer cell proliferation and glucan-induced granuloma formation in mice depleted of blood monocytes by strontium-89. J. Leukocyte Biol. 1990; 47: 195-205.
59. Swayer RT. The significance of local resident pulmonary alveolar macrophage proliferation in population renewal. J. Leukocyte Biol. 1986; 39: 77-87.
60. Swayer RT, Strausbauch PH, Volkman A. Resident macrophage proliferation in mice depleted of blood monocytes by strontium-89. Lab. Invest. 1982; 46: 165-170.
61. Novak JP, Skamene E, Gervais F. Quantitative model of mononuclear phagocyte lineage proliferation in murine bone marrow. J. Leukocyte Biol. 1989; 46: 25-33.
62. Travassoli M, Yoffey JM, eds. Bone Marrow: Structure and Function. Alan R Liss, Inc., New York, 1983.
63. Yoshida H, Hayashi SI, Kunisada T et al. The murine mutation 'osteopetrosis' (op) is a mutation in the coding region of the macrophage colony stimulating factor (Csfm) gene. Nature 1990; 345: 442-443.
64. Wiktor-Jedrejczak W, Bartocci A, Ferrante AW Jr et al. Total absence of colony-stimulating factor in the macrophage-deficient osteopetrotic (op/op) mouse. Proc. Natl Acad. Sci. USA 1990; 87: 4828-4832.
65. Naito M, Hayashi SI, Yoshida H et al. Abnormal differentiation of tissue macrophage populations in 'osteopetrosis' (op) mice defective in the production of macrophage colony-stimulating factor. Am. J. Pathol. 1991; 139: 657-667.
66. Wiktor-Jedrejczak W, Urbanowska E, Aukerman SL et al. Correction by CSF-1 of the defects in the osteopetrotic op/op mouse suggests local, developmental, and humoral requirements for this growth factor. Exp. Hematol. 1991; 19: 1049-1054.
67. Wiktor-Jedrejczak W, Ratajczak MZ, Ptasznik A et al. CSF-1 deficiency in the op/op mouse has differential effects on macrophage populations and differentiation stages. Exp. Hematol. 1992; 20: 1004-1010.
68. Wiktor-Jedrejczak W, Urbanowska E, Szperl M. Granulocyte-macrophage colony-stimulating factor corrects macrophage deficiencies, but not osteopetrosis in the colony-stimulating factor-1-deficient op/op mouse. Endocrinology 1994; 134: 1932-1935.
69. Takahashi K, Naito M, Umeda S et al. The role of macrophage colony-stimulating factor in hepatic glucan-induced granuloma formation in the osteopetrosis mutant mouse defective in the production of macrophage colony stimulating factor. Am. J. Pathol. 1994; 144: 1381-1392.
70. Cecchi MG, Domingo MG, Mocci S et al. Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse. Development 1994; 120: 1357-1372.
71. Umeda S, Takahashi K, Naito M et al. Neonatal changes of osteoclasts in osteopetrosis (op/op) mice defective in production of functional macrophage colony-stimulating factor (M-CSF) protein and effects of M-CSF on osteoclast development and differentiation. J. Submicrosc. Cytol. Pathol. 1996; 28: 13-26.
72. Wiktor-Jedrejczak W. In vivo role of macrophage growth factors as delineated using CSF-1 deficient op/op mouse. Leukemia 1993; 7 (Suppl. 2): 117-121.
73. Takahashi K, Umeda S, Shultz DL et al. Effects of macrophage colony-stimulating factor (M-CSF) on the development, differentiation, and maturation of marginal metallophilic macrophages and marginal zone macrophages in the spleen of osteopetrosis (op) mutant mice lacking functional M-CSF activity. J. Leukocyte Biol. 1994; 55: 581-588.
74. Metcalf C. Granulocyte-macrophage colony-stimulating factor transgenic mice. In: Jacob CO, ed. Overexpression and Knockout of Cytokines in Transgenic Mice. Academic Press, London, 1994; 161-186.
75. Akagawa KS, Kamoshita K, Tokunaga T. Effects of granulocyte/macrophage colony stimulating factor and colony stimulations factor-1 on the proliferation and differentiation of murine alveolar macrophages. J. Immunol. 1988; 141: 3383-3390.
76. Nakata K, Akagawa KS, Fukuyama M et al. Granulocyte/macrophage colony-stimulating factor promotes the proliferation of human alveolar macrophages in vitro. J. Immunol. 1991; 147: 1266-1272.
77. Dranoff G, Crawford AD, Sadelain M et al. Involvement of granulocyte-macrophage colony-stimulating factor in pulmonary homeostasis. Science 194; 264: 713-716.
78. Stanley E, Lieschke GJ, Crail D et al. Granulocyte/macrophage colony-stimulating factor-deficient mice show no major perturbation of hematopoiesis but develop a characteristic pulmonary pathology. Proc. Natl Acad. Sci. USA 1994; 91: 5592-5596.
79. Lieschke GJ, Stanley E, Grail D et al. Mice lacking both macrophage- and granulocyte-macrophage colony stimulating factor have macrophages and coexistent osteopetrosis and severe lung disease. Blood 1994; 84: 27-35.
80. Morioka Y, Naito M, Sato T et al. Immunophenotypic and ultrastructural heterogeneity of macrophage differentiation in bone marrow and fetal hematopoiesis of mouse in vitro and in vivo. J. Leukocyte Biol. 1994; 55: 642-651.
81. 89Sr. Am. J. Pathol. 1987; 127: 75-82.
82. Shibata Y, Volkman A. Restoration of prostaglandin releasing macrophage populations in lethally irradiated mice with spleen cells from bone marrow-depleted donors. J. Leukocyte Biol. 191; 49: 397-406.
83. McCormack JM, Leenen PJM, Walker WS. Macrophage progenitors from mouse bone marrow and spleen differ in their expression of the Ly-6C differentiation antigen. J. Immunol. 1993; 151: 6389-6398.
84. Moore MAS, Metcalf PJ. Ontogeny of the hematopoietic system: Yolk sac origin of in vitro colony-stimulating cells in the developing mouse embryo. Br. J. Haematol. 1970; 18: 279-296.
85. Cline MJ, Moore MAS. Embryonic origin of the mouse macrophages. Blood 1972; 39: 842-849.
86. Kelemen E, Calvo W, Fliedner TM, eds. Atlas of Human Hematopoietic Development. Springer-Verlag, Berlin, 1979.
87. 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. Leukocyte Biol. 1989; 45: 87-96.
88. Takahashi K, Naito M. Development, differentiation, and proliferation of macrophages in the rat yolk sac. Tissue Cell 1993; 25: 351-362.
89. Leenen PJM, Melis M, Slicker WAT et al. Murine macrophage precursor characterization. II. Monoclonal antibodies against macrophage precursor antigens. Eur. J. Immunol. 1990; 20: 27-34.
90. Slieker WAT, de Bruijn MFTR, Leenen PJM et al. ER-MP12 antigen, a new cell surface marker on mouse bone marrow cells with thymus-repopulating ability: Intrathymic repopulating ability of ER-MP12-positive bone marrow cells. Int. Immunol. 1993; 5: 1093-1098.
91. de Bruijn MFTR, Slieker WAT, van der Loo JCM et al. Distinct mouse bone marrow macrophage precursors identified by differential expression of ER-MP12 and ER-MP20 antigens. Eur. J. Immunol. 1994; 24: 2279-2289.
92. Leenen PJM, de Bruijn MFTR, Voerman JSA et al. Markers of mouse macrophage development detected by monoclonal antibodies. J. Immunol. Methods 1994; 174: 5-19.
93. Naito M, Yamamura F, Nishikawa SI et al. Development, differentiation, and maturation of fetal mouse yolk sac macrophages in cultures. J. Leukocyte Biol. 1989; 46: 1-10.
94. Naito M, Takahashi K, Nishikawa SI. Development, differentiation, and maturation of macrophages in the fetal mouse liver. J. Leukocyte Biol. 1990; 48: 27-37.
95. Naito M, Takahashi K, Takahashi H et al. Ontogenetic development of Kupffer cells. In: Knook DL, Wisse E, eds. Sinusoidal Liver Cells. Elsevier Biochemical Press, Amsterdam, 1982; 155-164.
96. Naito M, Yamamura F, Takeya M et al. Ultrastructural analysis of Kupffer cell progenitors. In: Kirn A, Knook DL, Wisse E, eds. Cells of the Hepatic Sinusoid, Vol. 1. Kupffer Cell Foundation, Rijwijk, 1986; 13-20.
97. Naito M, Takahashi K, Nishikawa SI. Yolk sac macrophages: A possible Kupffer cell precursor in the fetal mouse liver. In: Wisse E, Knook DL, Decker K, eds. Cells of the Hepatic Sinusoid, Vol. 2. Kupffer Cell Foundation, Rijwijk, 1989; 419-420.
98. Takahashi K, Naito M, Katabuchi H et al. Development, differentiation, and maturation of macrophages in the chorionic villi of mouse placenta with special reference to the origin of Hoffbauer cells. J. Leukocyte Biol. 1991; 50: 57-68.
99. Takahashi K, Sakuma H, Naito M et al. Cytological characters, transformation, and ontogenesis of dermal histiocytes and fibroblasts. Acta Pathol. Jpn. 1980; 30: 743-766.
100. Takahashi K, Takahashi H, Naito M et al. Ultrastructural and functional development of macrophages in the dermal tissue of rat fetuses. Cell Tissue Res. 1983; 232: 539-552.
101. Izumi S, Takeya M, Takagi K et al. Ontogenetic development of synovial A cells in fetal and neonatal rat knee joints. Cell Tissue Res. 1990; 262: 1-8.
102. Takeya M, Takahashi K. Ontogenetic development of macrophage subpopulations and Ia-positive dendritic cells in fetal and neonatal rat spleen. J. Leukocyte Biol. 1992; 52: 516-523.
103. Higashi K, Naito M, Takeya M et al. Ontogenetic development, differentiation, and phenotypic expression of macrophages in the fetal rat lungs. J. Leukocyte Biol. 1992; 51: 444-454.
104. Sorokin SP, Hoyt RF Jr. Pure population of nonmonocyte-derived macrophages arising in organ cultures of embryonic rat lungs. Anat. Rec. 1987; 217: 35-52.
105. Sorokin SP, Hoyt RF Jr, Grant MM. Development of macrophages in the lungs of fetal rabbits, rats, and hamsters. Anat. Rec. 1984; 209: 103-121.
106. Sorokin SP, Kobzik L, Hoyt RF Jr et al. Development of surface membrane characteristics of 'premedullary' macrophages in organ cultures of embryonic rat and hamster lungs. J. Histochem. Cytochem. 1989; 37: 365-376.
107. Sorokin SP, McNelly NA, Hoyt RF. CFU-rAM, the origin of lung macrophages, and the macrophage lineage. Am. J. Physiol. 1992; 263: 299-307.
108. Sorokin SP, McNelly NA, Hoyt RF Jr. Exogenous cytokines enhance survival of macrophages from organ cultured embryonic rat tissues. Anat. Rec. 1994; 240: 398-406.
109. Sorokin SP, Nancy NA, Hoyt RA et al. Precursors of macrophages in embryonic rat lungs fail to exhibit granulocyteforming potential. Anat. Rec. 1994; 240: 38-397.
110. Malorny U, Michels E, Sorg C. A monoclonal antibody against an antigen present on mouse macrophages and absent from monocytes. Cell Tissue Res. 1986; 243: 421-428.
111. Wake K, Decker K, Kim A et al. Cell biology and kinetics of Kupffer cells in the liver. Int. Rev. Cytol. 1989; 118: 173-229.
112. Fossum S. The life history of dendritic leukocytes (DL). In: Iversen OH, ed. Cell Kinetics of the Inflammatory Reaction, Springer-Verlag, Berlin, 1989; 101-124.
113. Tew JG. Follicular dendritic cells and dendritic cell nomenclature. In: Kamperdijk EWA, Nieuwenhuis P, Hoefsmit ECM, eds. Dendritic Cells in Fundamental and Clinical Immunology. Plenum Press, New York, 1993; 467-468.
114. Takahashi K, Sakashita N. Experimental analysis on origin of interdigitating cells in popliteal lymph nodes of mice by ligation of afferent lymphatics. Dendritic Cells 1994; 4: 139-143.
115. Janossy G, Bofill M, Poulter LW et al. Separate ontogeny of two macrophage-like accessory cell populations in the human fetus. J. Immunol. 1986; 136: 4354-4361.
116. Takahashi K, Naito M, Takeya M et al. Primitive/fetal macrophage population is a precursor of interdigitating cells in the fetal rat thymus during early ontogeny. In: Imai T, Tew JG, Hoefsmit ECM, eds. Dendritic Cells in Lymphoid Tissues. Excerpta Medica, Amsterdam, 1991; 191: 253-254.
117. Takahashi K, Takeya M, Hsiao K et al. Ontogenetic development of Langerhans cell lineage in the thymus and skin of rat fetuses and newborn infants. In: Thivolet J, Schmitt D, eds. Langerhans Cell. John Libbey Eurotext, London, 1988; 21-31.
118. Hsiao L, Takahashi K, Takeya M et al. Differentiation and maturation of macrophages into interdigitating cells and their multicellular complex formation in the fetal and postnatal rat thymus. Thymus 1991; 17: 219-235.
119. Hsiao L, Takeya M, Arao T et al. An immunohistochemical and immunoelectron microscopic study of the ontogeny of rat Langerhans cell lineage with anti-macrophage and anti-Ia monoclonal antibodies. J. Invest. Dermatol. 1989; 93: 780-786.
120. Mizoguchi S, Takahashi K, Takeya M et al. Development, differentiation, and proliferation of epidermal Langerhans cells in rat ontogeny studied by a novel monoclonal antibody against epidermal Langerhans cells, RED-1. J. Leukocyte Biol. 1992; 52: 52-61.
121. Takahashi K, Araki M, Miyakawa K. Development and distribution of T cell-associated dendritic cells in organs and tissues of mice depleted of blood monocytes by administration of strontium-89. In: Banchereau J, Schmitt D, eds. Dendritic Cells in Fundamental and Clinical Immunology. Plenum Press Inc., New York, 1995; 155-157.
122. Takahashi K, Naito M, Shultz LD et al. Differentiation of dendritic cell populations in macrophage colony-stimulating factor-deficient mice homozygous for the osteopetrosis (op) mutation. J. Leukocyte Biol. 1993; 53: 19-28.
123. Witmer-Pack MD, Olivier W, Vlinsky J et al. Granulocyte/macrophage colony stimulating factor is essential for the viability and function of cultured murine epidermal Langherhans cells. J. Exp. Med. 1987; 166: 1484-1498.
124. Steinman RM, Koide S, Witmer M et al. The sensitization phase of T cell-mediated immunity. Ann. N.Y. Acad. Sci. 1988; 546: 80-90.
125. Inaba K, Steinman RM, Witmer-Pack M et al. Identification of proliferating dendritic cell precursors in mouse blood. J. Exp. Med. 1992; 175: 1157-1167.
126. Inaba K, Inaba M, Romani N et al. Generation of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony stimulating factor. J. Exp. Med. 1992; 176: 1693-1702.
127. Umezu H, Naito M, Inaba K et al. Ultrastructural and immunophenotypic differentiation of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony-stimulating factor (GM-CSF). J. Submicrosc. Cytol. Pathol. 1995; 27: 227-234.
128. Takahashi K, Naito M, Inaba K et al. Development and differentiation of dendritic cells: Two functionally related but ultrastructurally distinct dendritic cell subpopulations. Dendritic Cells 1995; 5: 1-5.
129. Caux C, Denzutter-Dambuyant C, Schmitt D et al. GM-CSF and TNF-a cooperate in the generation of dendritic Langerhans cells. Nature 1992; 360: 258-261.
130. + derived dendritic/Langerhans cells. In: Banchereau J, Schmitt D, eds. Dendritic Cells in Fundamental and Clinical Immunology. Plenum Press Inc., New York, 1995; 1-5.
131. Rossi G, Heveker N, Thiele H et al. Development of a Langerhans cell phenotype from peripheral blood monocytes. Immunol. Lett. 1992; 31: 189-197.
132. Kasirerk W, Baumruker T, Majdic O et al. CD1 molecule expression on human monocytes induced by granulocyte-macrophage colony-stimulating factor. J. Immunol. 193; 150: 579-594.
133. Sallusto F, Lanzavecchia A. Efficient expression of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha. J. Exp. Med. 1994; 179: 1109-1118.