Osteoporosis of hematologic etiology

Experimental Hematology

Volumn 35, Issue 1, 2007, Pages 128-136

  Gurevitch, Olga ^a   Khitrin, Sofia ^a   Valitov, Andrei ^a   Slavin, Shimon ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

AGING; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BLEEDING; BONE MARROW; BONE TISSUE; C57BL 6 MOUSE; EXPERIMENTAL ANIMAL; HISTOLOGY; KIDNEY CAPSULE; LUMBAR VERTEBRA; MALE; MICROENVIRONMENT; MORPHOMETRICS; MOUSE; MOUSE STRAIN; NONHUMAN; ORGAN DONOR; OSSIFICATION; OSTEOLYSIS; OSTEOPOROSIS; PHLEBOTOMY; PLASMA; POSTMENOPAUSE; PRIORITY JOURNAL; RADIATION DOSE; RISK FACTOR; SENESCENCE; WHOLE BODY RADIATION;

AGE FACTORS; ANIMALS; BONE REGENERATION; BONE RESORPTION; HEMATOPOIESIS; HEMATOPOIETIC SYSTEM; HEMORRHAGE; LUMBAR VERTEBRAE; MICE; MICE, INBRED C57BL; OSTEOPOROSIS; WHOLE-BODY IRRADIATION;

EID: 33845783353     PISSN: 0301472X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.exphem.2006.09.010     Document Type: Article

References (61)

1. Parfitt A.M. Osteonal and hemi-osteonal remodeling: the spatial and temporal framework for signal traffic in adult human bone. J Cell Biochem 55 (1994) 273-286
2. Fleming L.A. Osteoporosis: clinical features, prevention, and treatment. J Gen Intern Med 7 (1992) 554-562
3. Mazess R.B. On aging bone loss. Clin Orthop Relat Res 165 (1982) 239-252
4. Chertkov J.L., Gurevitch O., and Udalov G.A. Role of bone marrow stroma in hemopoietic stem cell regulation. Exp Hematol 8 (1980) 770-778
5. Smith B.R. Regulation of hematopoiesis. Yale J Biol Med 63 (1990) 371-380
6. Clark B.R., and Keating A. Biology of bone marrow stroma. Ann N Y Acad Sci 770 (1995) 70-78
7. Visnjic D., Kalajzic Z., Rowe D.W., Katavic V., Lorenzo J., and Aguila H.L. Hematopoiesis is severely altered in mice with an induced osteoblast deficiency. Blood 103 (2004) 3258-3264
8. Gurevitch O., Drize N.J., Udalov G.A., and Chertkov J.L. The influence of hematopoiesis on the precursor cells of bone marrow stroma. Bull Exp Biol Med 10 (1982) 115-117 (in Russian; summary in English)
9. Kagawa J., Hayashi K., and Awai M. Participation of bone marrow stromal cells in hemopoietic recovery of rats irradiated and then parabiosed with a non-irradiated litter mate. I. Light microscopic observations. Acta Pathol Jpn 36 (1986) 999-1010
10. Hayashi K., Kagawa K., Awai M., and Irino S. The role of marrow architecture and stromal cells in the recovery process of aplastic marrow of lethally irradiated rats parabiosed with healthy litter mates. Scan Electron Microsc Pt 4 (1986) 1489-1499
11. Hirano T., and Iwasaki K. Bone marrow plays a role in bone metabolism: histomorphometry of iliac bone in postmenopausal women. Calcif Tissue Int 51 (1992) 348-351
12. Marley S.B., Lewis J.L., Davidson R.J., et al. Evidence for a continuous decline in haemopoietic cell function from birth: application to evaluating bone marrow failure in children. Br J Haematol 106 (1999) 162-166
13. Morrison S.J., Wandycz A.M., Akashi K., Globerson A., and Weissman I.L. The aging of hematopoietic stem cells. Nat Med 2 (1996) 1011-1016
14. Bergman R.J., Gazit D., Kahn A.J., Gruber H., McDougall S., and Hahn T.J. Age-related changes in osteogenic stem cells in mice. J Bone Miner Res 11 (1996) 568-577
15. Kahn A., Gibbons R., Perkins S., and Gazit D. Age-related bone loss. A hypothesis and initial assessment in mice. Clin Orthop Relat Res 313 (1995) 69-75
16. Domenech J., Gihana E., Dayan A., et al. Haemopoiesis of transplanted patients with autologous marrows assessed by long-term marrow culture. Br J Haematol 88 (1994) 488-496
17. O'Flaherty E., Sparrow W., and Szer J. Bone marrow stromal function from patients after bone marrow transplantation. Bone Marrow Transplant 15 (1995) 207-212
18. Domenech J., Roingeard F., Herault O., et al. Changes in the functional capacity of marrow stromal cells after autologous bone marrow transplantation. Leuk Lymphoma 29 (1998) 533-546
19. Knospe W.H., Husseini S.G., Adler S.S., and Reddi A.H. Decalcified tooth matrix powder induces new bone formation and hematopoietic microenvironment in the mouse. Int J Cell Cloning 3 (1985) 320-329
20. Gurevitch O.A. The ability of induced osteo-progenitor cells to maintain and rebuild long-term ectopic osteo-hematopoietic foci in vivo. Int J Cell Cloning 8 (1990) 130-137
21. Gurevitch O.A., Samoilina N.L., Medvinsky A.L., and Gun O.I. Induction of ectopic osteohemopoietic foci in mice on implantation of demineralized tooth matrix. Gematol Transfuziol N2 (1990) 7-12 (in Russian)
22. Maniatis A., Tavassoli M., and Crosby W.H. Origin of osteogenic precursor cells in extramedullary marrow implants. Blood 38 (1971) 569-575
23. Udalov G.A., Gurevitch O.A., and Chertkov J.L. The origin of hemopoietic cells in syngeneic and semisyngeneic ectopic hemopoietic site. Bull Exp Biol Med 5 (1977) 584-586 (in Russian; summary in English)
24. Gurevitch O.A., and Fabian I. Ability of the hemopoietic microenvironment in the induced bone to maintain the proliferative potential of early hemopoietic precursors. Stem Cells 11 (1993) 56-61
25. Sadr A.M., Cardenas F., and Tavassoli M. Functional potential of ectopic marrow autotransplants. Experientia 36 (1980) 605-606
26. Tavassoli M., Maniatis A., and Crosby W.H. The effects of phenylhydrazine-induced haemolysis on the behavior of regenerating marrow stroma. Br J Haematol 23 (1972) 707-711
27. Sampath T.K., and Reddi A.H. Homology of bone-inductive proteins from human, monkey, bovine, and rat extracellular matrix. Proc Natl Acad Sci U S A 80 (1983) 6591-6595
28. Schmitt J.M., Hwang K., Winn S.R., et al. Bone morphogenetic proteins: an update on basic biology and clinical relevance. J Orthop Res 17 (1999) 269-278
29. Gurevitch O., Gowda S., Kurkalli B., et al. Reconstruction of cartilage, bone, and hematopoietic microenvironment with demineralized bone matrix and bone marrow cells. Stem Cells 21 (2003) 588-597
30. Karlsson M.K., Ahlborg H.G., and Karlsson G. Pregnancy and lactation are not risk factors for osteoporosis or fractures. Lakartigningen 1022 (2005) 290-293
31. Watrous D.A., and Andrews B.S. The metabolism and immunology of bone. Semin Arthritis Rheum 19 (1989) 46-65
32. Feng X. Regulatory roles and molecular signaling of TNF family members in osteoclasts. Gene 350 (2005) 1-13 (Review)
33. Vaananen K. Mechanism of osteoclast mediated bone resorption-rationale for the design of new therapeutics. Adv Drug Deliv Rev 57 (2005) 959-971
34. Gurevitch O.A., and Chertkov J.L. Factors influencing the function of the cells transferring hematopoietic microenvironment. Probl Gematol Pereliv Krovi 8 (1980) 43-48 (in Russian)
35. Burkhardt R., Kettner G., Bohm W., et al. Changes in trabecular bone, hematopoiesis and bone marrow vessels in aplastic anemia, primary osteoporosis, and old age: a comparative histomorphometric study. Bone 8 (1987) 157-164
36. Mahachoklertwattana P., Chuansumrit A., Sirisriro R., Choubtum L., Sriphrapradang A., and Rajatanavin R. Bone mineral density, biochemical and hormonal profiles in suboptimally treated children and adolescents with beta-thalassaemia disease. Clin Endocrinol (Oxf) 58 (2003) 273-279
37. Zaino E.C. Pathophysiology of thalassemia. Ann N Y Acad Sci 344 (1980) 284-304
38. Sanner J.R., and Ramin J.E. Osteoporotic, hematopoietic mandibular marrow defect: an osseous manifestation of sickle cell anemia. J Oral Surg 35 (1977) 986-988
39. Seidler R.C., and Becker J.A. Intrathoracic extramedullary hematopoiesis. Radiology 83 (1964) 1057-1059
40. Coventry W.D., and LaBree R.H. Heterotopia of bone marrow simulating mediastinal tumor: a manifestation of chronic hemolytic anemia in adults. Annals of Internal Medicine 53 (1960) 1042-1052
41. Knoblich R. Extramedullary hematopoiesis presenting as intrathoracic tumors. Report of a case in a patient with thalassemia minor. Cancer 13 (1960) 462-468
42. Gurevitch O.A. Extraskeletal bone formation and induced osteogenesis (Review). Gematol Transfuziol 34 (1989) 41-47 (in Russian)
43. Gallacher S.J., Deighan C., Wallace A.M., et al. Association of severe haemophilia A with osteoporosis: a densitometric and biochemical study. Q J Med 87 (1994) 181-186
44. Barnes C., Wong P., Egan B., et al. Reduced bone density among children with severe hemophilia. Pediatrics 114 (2004) e177-e181
45. Bernardi E., and Prandoni P. Safety of low molecular weight heparins in the treatment of venous thromboembolism. Expert Opin Drug Saf 2 (2003) 87-94
46. Pettila V., Leinonen P., Markkola A., Hilesmaa V., and Kaaja R. Postpartum bone mineral density in women treated for thromboprophylaxis with unfractionated heparin or LMW heparin. Thromb Haemost 87 (2002) 182-186
47. Lippiello L., Chavda D., and Connolly J. Colony-forming efficiency response of bone marrow stromal cells to acute blood loss. J Orthop Res 10 (1992) 145-148
48. Ilizarov G.A., Chepelenko T.A., Izotova S.P., and Kochetkov I.S. Effect of acute blood loss on stromal regulation of hematopoietic stem cells and reparative bone regeneration. Patol Fiziol Eksp Ter (1986) 54-58
49. Rothstein G. Disordered hematopoiesis and myelodysplasia in the elderly. J Am Geriatr Soc 51 3 suppl (2003) S22-S26
50. Ershler W.B. Biological interactions of aging and anemia: a focus on cytokines. J Am Geriatr Soc 51 3 suppl (2003) S18-S21
51. Carmel R. Anemia and aging: an overview of clinical, diagnostic and biological issues. Blood Rev 15 (2001) 9-18
52. Chertkov J.L., and Gurevitch O.A. Age-related changes in hemopoietic microenvironment. Enhanced growth of hemopoietic stroma and weakened genetic resistance of hemopoietic cells in old mice. Exp Gerontol 16 (1981) 195-198
53. Chertkov JL, Drize NJ, Gurevitch OA. Hemopoietic microenvironment and hemopoietic stroma precursors. In: Hollan SR, et al., eds. Recent Advances in Haematology, Immunology and Blood Transfusion. Akademiai Kiado, Budapest: 1982. p. 133-147.
54. Torricelli P., Fini M., Giavaresi G., Rimondini L., and Giardino R. Characterization of bone defect repair in young and aged rat femur induced by xenogenic demineralized bone matrix. Recent Advances in Haematology, Immunology, and Blood Transfusion 73 (2002) 1003-1009
55. Hollinger J.O., Winn S., and Bonadio J. Options for tissue engineering to address challenges of the aging skeleton. Tissue Eng 6 (2000) 341-350
56. Gurevitch O., and Slavin S. The hematological etiology of osteoporosis. Med Hypotheses 67 (2006) 729-735
57. Jilka R.J., Takahashi K., Munshi M., Williams D.C., Roberson P.K., and Manolagas S.C. Loss of estrogen upregulates osteoblastogenesis in the murine bone marrow. Evidence for autonomy from factors released during bone resorption. J Clin Invest 101 (1998) 1942-1950
58. Jilka R.L., Hangoc G., Girasole G., et al. Increased osteoclast development after estrogen loss: mediation by interleukin-6. Science 257 (1992) 88-91
59. Syed F., and Khosla S. Mechanisms of sex steroid effects on bone. Biochem Biophys Res Commun 328 (2005) 688-696
60. Parikka V., Lehenkari P., Sassi M.L., et al. Estrogen reduces the depth of resorption pits by disturbing the organic bone matrix degradation activity of mature osteoclasts. Endocrinology 142 (2001) 5371-5378
61. Piva R., Penolazzi L., Lambertini E., Giordano S., and Gambari R. Induction of apoptosis of human primary osteoclasts treated with a transcription factor decoy mimicking a promoter region of estrogen receptor alpha. Apoptosis 10 (2005) 1079-1094