Retroviruses and bone diseases

Clinical Orthopaedics and Related Research

Volumn 326, Issue , 1996, Pages 287-309

  Labat, Marie Louise ^a,b  

^a CNRS   (France)

^b CENTRE DE RECHERCHE DES CORDELIERS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COLONY STIMULATING FACTOR 1; HLA DR ANTIGEN; ZIDOVUDINE;

ALBERS SCHOENBERG DISEASE; BONE ATROPHY; BONE TUMOR; CONFERENCE PAPER; DEVELOPMENTAL DISORDER; GENE EXPRESSION; GENETIC DISORDER; HOST RESISTANCE; HUMAN; IMMUNE DEFICIENCY; LEUKEMIA VIRUS; MONONUCLEAR CELL; NONHUMAN; OSTEOMA; PAGET BONE DISEASE; PRIORITY JOURNAL; RETROVIRUS; VIRUS GENOME; VIRUS REPLICATION;

EID: 0029922918     PISSN: 0009921X     EISSN: 15281132     Source Type: Journal    
DOI: 10.1097/00003086-199605000-00036     Document Type: Conference Paper

References (110)

1. Albers-Schönberg HE: Rontgenbilder einer seltenen. Knochenerkrankung Muenchen Med Wochenschr 51:365, 1904.
2. Anderson LJ, Jarrett WFH, Jarrett O, et al: Feline leukemia-virus infection of kittens: Mortality associated with atrophy of the thymus and lymphoid depletion. J Natl Cancer Inst 47:807-817, 1971.
3. Ballet JJ, Griscelli C, Coutris G, et al: Bone-marrow transplantation in osteopetrosis. Lancet 2:1137, 1977.
4. Baltimore D: RNA-dependent DNA polymerase in virions of RNA tumor viruses. Nature 226: 1209-1210, 1970.
5. Banes AJ, Smith RE: Biological characterization of avian osteopetrosis. Infect Immun 16:876-884, 1977.
6. Barré-Sinoussi F, Chermann J-C, Rey FN, et al: Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science 220:868-871, 1983.
7. Bonadio J, Saunders TL, Tsai E, et al: A transgenic model of osteogenesis imperfecta type 1. Proc Natl Acad Sci U S A 87:7145-7149, 1990.
8. Boyce BF, Chen H, Soriano P, et al: Histomorphometric and immunocytochemical studies of src-related osteopetrosis. Bone 14:335-340, 1993.
9. Boyde A, Banes AJ, Dillaman RM, et al: A morphological study of an avian bone disorder caused by myeloblastosis associated viruses. Metabolic Bone Disease 1:235-242, 1978.
10. Brighton CT, Lorich DG, Kupcha R, et al: The pericyte as a possible osteoblast progenitor cell. Clin Orthop 275:287-299, 1992.
11. Bringuier AF, Labat ML: Retroviral expression in a patient who has paraarticular ossification. Clin Orthop 313:239-252, 1995.
12. Bringuier AF, Séébold-Choqueux C, Moricard Y, et al: T-lymphocyte control of HLA-DR blood monocyte differentiation into neo-fibroblasts. Further evidence of pluripotential secreting functions of HLA-DR monocytes, involving not only collagen but also uromodulin, amyloid -β peptide, α-fetoprotein and carcinoembryonic antigen. Biomed Pharmacother 46:91-108, 1992.
13. Browning PJ, Sechler JMG, Kaplan M, et al: Identification and culture of Kaposi's sarcoma-like spindle cells from the peripheral blood of human immunodeficiency virus-1-infected individuals and normal controls. Blood 84:2711-2720, 1994.
14. Buchberg AM, Jenkins NA, Copeland NG: Localization of the murine macrophage colony-stimulating factor gene to chromosome 3 using interspecific backcross analysis. Genomics 5:363-367, 1989.
15. Buck BE, Resnick L, Shah SM: Human immunodeficiency virus cultured from bone. Implications for transplantation. Clin Orthop 251:249-253, 1990.
16. Burny A, Bex F, Chantrenne H, et al: Bovine leukemia virus involvement in enzootic bovine leukosis. Adv Cancer Res 28:251-311, 1978.
17. Chandra P, Steel LK: Purification, biochemical characterization and serological analysis of cellular deoxyribonucleic acid polymerase and a reverse transcriptase from spleen of a patient with myelofibrotic syndrome. Biochem J 67:513-524, 1977.
18. Clements JE, Zink MC, Narayan O, et al: Lentivirus infection of macrophages. Immunol Ser 60: 589-600, 1994.
19. Copeland EA, Rinehart JJ, Lewis M, et al: The mechanism of retrovirus suppression of human T-cell proliferation in vitro. J Immunol 131: 2017-2020, 1983.
20. Cunningham NS, Paralkar V, Reddi AH: Osteogenin and recombinant bone morphogenetic protein 2B are chemotactic for human monocytes and stimulate transforming growth factor β1 mRNA expression. Proc Natl Acad Sci USA 89:11740-11744, 1992.
21. Dickie MM: 1967 Jackson Laboratory contribution. Mouse News Letter 38:39, 1967.
22. +1. J Immunol 136:3137-3139, 1986.
23. Finkel MP, Biskis BO, Jenkins PB: Virus induction of osteosarcoma in mice. Science 151:698-701, 1966.
24. Gabuzda DH, Hess L, Small JA, Clements JE: Regulation of the visna virus long terminal repeat in macrophages involves cellular factors that bind sequences containing AP-1 sites. Mol Cell Biol 9:2728-2733, 1989.
25. Gardner MB, Rongey RW, Arnstein P, et al: Experimental transmission of feline fibrosarcoma to cats and dogs. Nature 226:807-808, 1970.
26. Green MC: Catalog of Mutant Genes and Polymorphic Loci. In Lyon MF, Searle AG (eds). Genetic Variants and Strains of the Laboratory Mouse. New York, Oxford University Press 12-14, 1989.
27. Gross L: "Spontaneous" leukemia developing in C3H mice following inoculation in infancy, with Ak-leukemic extracts, or Ak-embryos. Proc Soc Exp Biol Med 76:27-32, 1951.
28. Grüneberg H: A new sub-lethal colour mutation in the house mouse. Proc R Soc Lond B Biol Sci 118:321-342, 1935.
29. Grüneberg H: The relations of microphthalmia and white in the mouse. J Genet 51:359-362, 1953.
30. Harbers K, Kuehn M, Delius H, et al: Insertion of retrovirus into the first intron of α1(I) collagen gene leads to embryonic lethal mutation in mice. Proc Natl Acad Sci U S A 81:504-1508, 1984.
31. Hebebrand LC, Olsen RG, Mathes LE, et al: Inhibition of human lymphocyte mitogen and antigen response by a 15,000 dalton protein from feline leukemia virus. Cancer Res 39:443-447, 1979.
32. Hertwig P: Sechs neue Mutationen bei der Hausmaus in ihrer Beeutung für allgemeine Vererbungsfragen. Ztschr F menschl Vererb u Konstitutionslehre 26:1-21, 1942.
33. Hochman N, Hojo H, Hojo S, et al: Reversal of immune dysfunction in osteopetrotic rats by interferon-gamma: Augmentation of macrophage Ia expression and lymphocyte interleukine-2 production and proliferation. Cell Immunol 137:14-23, 1991.
34. Hochman N, Wahl LM, Sandberg AL: Coexistence of defective and normal immunologic functions in lymphocytes and macrophages from osteopetrotic (op) rats. J Immunol 129:278-281, 1982.
35. Hodgkinson CA, Moore KJ, Nakayama A, et al: Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic -helix-loop-helix-zipper protein. Cell 74:395-404 1993.
36. Hoover EA, Kociba GJ: Bone lesions in cats with anemia induced by feline leukemia virus. J Natl Cancer Inst 53:1277-1284, 1974.
37. Horton WA, Schmike RN, Iyama T: Osteopetrosis: Further heterogeneity. J Pediatr 97:580-585, 1980.
38. Hufner M, Döhner H, Schmidt J: Evidence for an osteoclast-activating factor in a patient with peripheral T-cell lymphoma and osteosclerosis. Klin Wocheschr 67:402-407, 1989.
39. +Ha revenant alleles. J Cell Biol 4:2899-2904, 1984.
40. Ikeda S, Nishimura C, Tamura T, et al: Effect of steroid hormone on spontaneous production of progeny and virion-associated reverse-transcriptase of baboon endogenous virus. Kitasato Arch Exp Med 54:49-54, 1981.
41. Jähner D, Jaenisch R: Integration of Moloney leukaemia virus into the germ line of mice: Correlation between site of integration and virus activation Nature 287:456-458, 1985.
42. Jarrett WFH, Martin WB, Crighton GW, et al: Leukemia in the cat: Transmission experiments with leukemia (lymphosarcoma). Nature 202:566-567, 1964.
43. Jee WSS, Nolan PD: Origin of osteoclasts from the fusion of phagocytes. Nature 220:225-226, 1963.
44. Jenkins NA, Copeland NG, Taylor BA, et al: Dilute (d) coat color mutation of DBA/2J mice is associated with the site of integration of an ecotropic MuLV genome. Nature 293:370-374, 1981.
45. Johnson RS, Spiegelman BM, Papaioannou V: Pleiotropic effects of a null mutation in the c-fos proto-oncogene. Cell 71:577-586, 1992.
46. Joliot V, Boroughs K, Lasserre F, et al: Pathogenic potential of myeloblastosis-associated virus: Implication of ENV proteins for osteopetrosis induction. Virology 195:812-819, 1993.
47. Jungherr E, Landauer W: Studies on fowl paralysis. III. A condition resembling osteopetrosis (marble bone) in common fowl. Storrs Agricultural Experiment Station 222:1-34, 1938.
48. Kahn AJ, Simmons DJ: Investigation of cell lineage in bone using a chimera of chick and quail embryonic tissue. Nature 258:325-327, 1975.
49. Kaibara N, Katsuki I, Hotokebuchi T, et al: Intermediate form of osteopetrosis with recessive inheritance. Skeletal Radiol 9:47-51, 1982.
50. Kalyanaraman VS, Sarngadharan MG, Robert-Guroff M: A new subtype of human T-cell leukemia virus (HTLV-II) associated with a T-cell variant of hairy cell leukemia. Science 218:571-573, 1982.
51. Kaplan FS: Paget's disease of bone: Exploring the questions. Calcif Tissue Int 51:1-3, 1992.
52. Labat ML: Retroviruses, immunosuppression and osteopetrosis. Biomed Pharmacother 40:85-90, 1986.
53. Labat ML: A new approach to the study of the origin of genetic diseases: Retroviral etiology of osteopetrosis. Biomed Pharmacother 45:23-27, 1991.
54. Labat ML: Albers-Schönberg disease (osteopetrosis): From a developmental disease of bone to a pre T-cell leukemia syndrome involving a new retrovirus. An illustration of the interest of animal models. Cells Mat 1(suppl):59-68, 1991.
55. Labat ML, Bringuier AF, Arys-Philippart C, et al: Monocytic origin of fibrosis. In vitro transformation of HLA-DR monocytes into neo-fibroblasts: Inhibitory effect of all-trans retinoic acid on this process. Biomed Pharmacother 48:103-111, 1994.
56. Labat ML, Bringuier AF, Chandra A, et al: Retroviral expression in mononuclear blood cells isolated from a patient with osteopetrosis (Albers-Schönberg disease). J Bone Miner Res 5:425-435, 1990.
57. Labat ML, Bringuier AF, Séébold C, et al: Monocytic origin of fibroblasts: Spontaneous transformation of blood monocytes into neo-fibroblastic structures in osteomyelosclerosis and Englemann's disease. Biomed Pharmacother 45:289-299, 1991.
58. Labat ML, Milhaud G: Osteopetrosis and the Immune Deficiency Syndrome. In Peck WA(ed). Bone and Mineral Research. Vol 4. Amsterdam, Elsevier 131-212, 1986.
59. Labat ML, Moricard Y, Pene F, et al: Gene-dependent differences in malignant osteopetrosis as evidenced by cellular induction of the disease. Biomed Pharmacother 35:155-159, 1982.
60. Labat ML, Tzehoval E, Moricard Y, et al: Osteopetrosis: Animal Models Evidencing Relations Between Lymphocytes, Macrophages and Bone Remodeling. In Ornoy A, Harell A, Sela J (eds). Current Advance in Skeletogenesis. Proceedings of the Fifth Workshop on Calcified Tissues, Kyriat Anavim, Israel, 1984. Amsterdam, Elsevier 269-277, 1984.
61. Lamour Y: Alzheimer's disease: A review of recent findings. Biomed Pharmacother 48:312-318, 1994.
62. Lane PW: Jackson Laboratory contribution. Mouse News Letter 60:50, 1979.
63. Leib-Mosch C, Brack-Werner R, Werner T, et al: Endogenous retroviral elements in human DNA. Cancer Res 50(suppl):5636-5642, 1990.
64. Lowe C, Yoneda T, Boyce BF, et al: Osteopetrosis due to src deficiency is caused by an osteoclast defect. J Bone Miner Res 7:269-272, 1992.
65. Lyall EGH, Langdale-Brown B, Eden OB, et al: Ewing's sarcoma in a child with human immunodeficiency virus (type 1) infection. Med Pediatr Oncol 21:127-131, 1993.
66. Marks SC, Lane PW: Osteopetrosis, a new recessive skeletal mutation on chromosome 12 of the mouse. J Hered 67:11-18, 1976.
67. Maximow A: Cultures of blood leucocytes. From lymphocytes and monocytes to connective tissue. Archiv für Experimentelle Zellforschung 5:12-268, 1928.
68. Milhaud G, Labat ML: Thymus and Osteopetrosis. Clin Orthop 135:260-271, 1978.
69. Milhaud G, Labat ML, Graf B, et al: Démonstration cinétique, radiographique et histologique de la guérison de l'ostéopétrose congénitale du rat. C R Acad Sci Paris, Série D 280:2485-2488, 1975.
70. Milhaud G, Labat ML, Parant M, et al: Immunological defect and its correction in the osteopetrotic mutant rat. Proc Natl Acad Sci USA 74:339-342, 1977.
71. Milhaud G, Labat ML, Viegas-Pequignot E, et al: Migrations cellulaires au cours de la guérison provoquée de l'ostéopétrose du rat "op" et thymus. C R Acad Sci Paris, Série D 281:1929-1932, 1975.
72. Mellert W, Kleinschmidt A, Schmidt J, et al: Infection of human fibroblasts and osteoblast-like cells with HIV-1. AIDS 4:527-535, 1990.
73. Metchnikoff E: Leçons sur la pathologie comparée de l'inflammation Faites à l'Institute Pasteur en Avril et Mai 1891. Bibliothèque des Annales de l' Institut Pasteur G. Paris, Masson 111-315, 1892. Lectures on the Comparative Pathology of Inflammation. English translation: Starling FA, Starling EH. London, Kegan Paul, Trench, Trubner & Co 1893. Reprinted New York, Dover, 1968.
74. Metchnikoff E: Leçons sur la pathologie comparée de l'inflammation Faites à l'Institute Pasteur en Avril et Mai 1891. Bibliothèque des Annales de l' Institut Pasteur G. Paris, Masson 111-315, 1892. Lectures on the Comparative Pathology of Inflammation. English translation: Starling FA, Starling EH. London, Kegan Paul, Trench, Trubner & Co 1893. Reprinted New York, Dover, 1968.
75. Meyerson G, Dahl N, Pahlman S: Malignant osteopetrosis: C-src kinase is not reduced in fibroblasts. Calcif Tissue Int 53:69-70, 1993.
76. Miyoshi I, Kubonishi I, Yoshimoto S, et al: Type C virus particles in a cord T-cell line derived by co-cultivating normal human cord leukocytes and human leukaemic T cells. Nature 294:770-771, 1981.
77. Mokotura T, Fukumoto S, Takashi S, et al: Expression of parathyroid hormone-related protein in a human T-cell lymphotropic virus type 1-infected T-cell line. Biochem Biophys Res Commun 154: 1182-1183, 1988.
78. Monaghan BA, Kaplan FS, August CS, et al: Transient infantile osteopetrosis. J Pediatr 118:252-256, 1991.
79. Morgan DA, Ruscetti FW, Gallo RC: Selective in vitro growth of T-lymphocytes from normal human bone marrow. Science 193:1007-1008, 1976.
80. Murray AB, Schmidt J, Rieke L: Retrovirus-induced osteopetrotic mice. Ultrastructural evidence of early virus production in osteoblasts and osteocytes. Am J Pathol 124:319-323, 1986.
81. Noir BC, De Vico AL, Nakamura S, et al: Identification of a major growth factor for AIDS-Kaposi's sarcoma cells as oncostatin M. Science 13:1430-1432, 1992.
82. Nussey AM: Osteopetrosis. Arch Dis Child 13: 161-172, 1938.
83. Orchard PJ, Dahl N, Aukerman L, et al: Circulating macrophage colony-stimulating factor is not reduced in malignant osteopetrosis. Exp Hematol 20:103-105, 1992.
84. Owen M: Marrow stromal stem cells. J Cell Sci 10 (Suppl):63-76, 1988.
85. Philippart C, Tzehoval E, Moricard Y, et al: Immune cell defects affect bone remodeling in osteopetrotic op/op mice. Bone Miner 23:317-332, 1993.
86. Poiesz BJ, Ruscetti FW, Gazdar AF, et al: Detection and isolation of type-C retrovirus particles from fresh and cultured lymphocyte from a patient with cutaneous T-cell lymphoma. Proc Natl Acad Sci USA 77:7415-7419, 1980.
87. Popovic M, Sarngadharan MG, Read E, et al: Detection, isolation, and continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS. Science 234:497-500, 1984.
88. Robinson HL, Reinsch SS, Shank PR: Sequences near the 5′ long terminal repeat of avian leukosis viruses determine the ability to induce osteopetrosis. J Virol 59:45-49, 1986.
89. Rojko JL, Olsen RG: The Immunobiology of the Feline Leukemia Virus. In Bourne FJ, Gorman NT (eds). Advances in Veterinary Immunology. Amsterdam. Elsevier 107-165, 1983.
90. Roodman GD, Kurihara N, Ohsaki Y, et al: Interleukin 6: A potential autocrine/paracrine factor in Paget's disease of bone. J Clin Invest 89:46-52, 1992.
91. Rous P: A filtrable agent the cause of a second chicken tumor, an osteochondrosarcoma. JAMA 59:1793-1794, 1912.
92. Rubin P: Dynamic Classification of Bone Dysplasia. Chicago, Year Book Medical Publishers 391, 1964.
93. Ruddle NH, Li CB, Home WC, et al: Mice transgenic for HTLV-1 LTR-tax exhibit tax expression in bone, skeletal alterations, and high bone turnover. Virology 197:196-204, 1993.
94. Rüther U, Garber C, Komitowski D, et al: Deregulated c-fos expression interferes with normal bone development in transgenic mice. Nature 325:412-416, 1987.
95. Singer FR, Mills BR: Nuclear inclusions in Paget' disease of bone. Science 194:201-202, 1976.
96. Smith RE: Avian osteopetrosis. Curr Top Microbial Immunol 101:75-94, 1982.
97. Soriano P, Montgomery C, Geske R, et al: Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice. Cell 64:693-702, 1991.
98. Stehelin D, Varmus HE, Bishop JM: DNA related to the transforming gene(s) of avian sarcoma viruses, is present in normal avian DNA. Nature 260:170-173, 1976.
99. 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 Leukoc Biol 53:19-28, 1993.
100. Temin HM, Mizutani S: RNA-dependent DNA polymerase in virions of Rous sarcoma virus. Nature 226:1211-1214, 1970.
101. Urist MR: Bone: Bone formation by autoinduction. Science 150: 893-899, 1965.
102. Urist M: Bone morphodifferentiation and tumorigenesis. Perspect Biol Med 22:89-113, 1979.
103. Urist MR, Budy AM, McLean FC: Species differences in the reaction of the mammalian skeleton to estrogens. Proc Soc Exp Biol Med 68:324-326, 1948.
104. Urist MR, Budy AM, McLean FC: Endosteal bone formation in estrogen-treated mice. J Bone Joint Surg 32A:143-162, 1950.
105. Walker DG: Bone resorption restored in osteopetrotic mice by transplants of normal bone marrow and spleen cells. Science 190:784-785, 1975.
106. Walker DG: Bone resorption restored in osteopetrotic mice by transplant of normal bone marrow and spleen cells (Classic articles) Clin Orthop 294:4-6, 1993.
107. Weiss R, Teich N, Varmus H, et al (eds): RNA Tumor Viruses. Ed 2. New York, Cold Spring Harbor 1985.
108. Westarp ME, Westphal KP, Clausen J, et al: Retroviral interference with neurotrophic signaling in human motor neuron disease. Clin Physiol Biochem 10:1-7, 1973.
109. Wiktor-Jedzejczak W, Ahmed A, Szezylik C, Skelly RR: Hematological characterization of congenital osteopetrosis in op/op mouse. Possible mechanism for abnormal macrophage differentiation. J Exp Med 156:1516-1526, 1975.
110. Yoshida H, Hayashi S-I, Kunisada T, et al: The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene. Nature 345:442-443, 1990.