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The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1998 Apr 15;101(8):1737–1744. doi: 10.1172/JCI2361

Reproduction of human fibrous dysplasia of bone in immunocompromised mice by transplanted mosaics of normal and Gsalpha-mutated skeletal progenitor cells.

P Bianco 1, S A Kuznetsov 1, M Riminucci 1, L W Fisher 1, A M Spiegel 1, P G Robey 1
PMCID: PMC508756  PMID: 9541505

Abstract

We have isolated progenitor cells from the stromal system of the fibrous dysplastic marrow of patients with McCune-Albright Syndrome. Analysis of the Gsalpha gene from individual colonies provided direct evidence for the presence of two different genotypes within single fibrous dysplastic lesions: marrow stromal cells containing two normal Gsalpha alleles, and those containing one normal allele and an allele with an activating mutation. Transplantation of clonal populations of normal cells into the subcutis of immunocompromised mice resulted in normal ossicle formation. In contrast, transplantation of clonal populations of mutant cells always led to the loss of transplanted cells from the transplantation site and no ossicle formation. However, transplantation of a mixture of normal and mutant cells reproduced an abnormal ectopic ossicle recapitulating human fibrous dysplasia and providing an in vivo cellular model of this disease. These results provide experimental evidence for the necessity of both normal and mutant cells in the development of McCune-Albright Syndrome fibrous dysplastic lesions in bone.

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Selected References

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  1. Ashton B. A., Allen T. D., Howlett C. R., Eaglesom C. C., Hattori A., Owen M. Formation of bone and cartilage by marrow stromal cells in diffusion chambers in vivo. Clin Orthop Relat Res. 1980 Sep;(151):294–307. [PubMed] [Google Scholar]
  2. Bradbeer J. N., Riminucci M., Bianco P. Giemsa as a fluorescent stain for mineralized bone. J Histochem Cytochem. 1994 May;42(5):677–680. doi: 10.1177/42.5.7512588. [DOI] [PubMed] [Google Scholar]
  3. Candeliere G. A., Glorieux F. H., Prud'homme J., St-Arnaud R. Increased expression of the c-fos proto-oncogene in bone from patients with fibrous dysplasia. N Engl J Med. 1995 Jun 8;332(23):1546–1551. doi: 10.1056/NEJM199506083322304. [DOI] [PubMed] [Google Scholar]
  4. Danon M., Crawford J. D. The McCune-Albright syndrome. Ergeb Inn Med Kinderheilkd. 1987;55:81–115. doi: 10.1007/978-3-642-71052-0_3. [DOI] [PubMed] [Google Scholar]
  5. Friedenstein A. J., Chailakhyan R. K., Gerasimov U. V. Bone marrow osteogenic stem cells: in vitro cultivation and transplantation in diffusion chambers. Cell Tissue Kinet. 1987 May;20(3):263–272. doi: 10.1111/j.1365-2184.1987.tb01309.x. [DOI] [PubMed] [Google Scholar]
  6. Friedenstein A. J., Piatetzky-Shapiro I. I., Petrakova K. V. Osteogenesis in transplants of bone marrow cells. J Embryol Exp Morphol. 1966 Dec;16(3):381–390. [PubMed] [Google Scholar]
  7. Gettys T. W., Ramkumar V., Uhing R. J., Seger L., Taylor I. L. Alterations in mRNA levels, expression, and function of GTP-binding regulatory proteins in adipocytes from obese mice (C57BL/6J-ob/ob). J Biol Chem. 1991 Aug 25;266(24):15949–15955. [PubMed] [Google Scholar]
  8. Goshima J., Goldberg V. M., Caplan A. I. Osteogenic potential of culture-expanded rat marrow cells as assayed in vivo with porous calcium phosphate ceramic. Biomaterials. 1991 Mar;12(2):253–258. doi: 10.1016/0142-9612(91)90209-s. [DOI] [PubMed] [Google Scholar]
  9. Happle R. The McCune-Albright syndrome: a lethal gene surviving by mosaicism. Clin Genet. 1986 Apr;29(4):321–324. doi: 10.1111/j.1399-0004.1986.tb01261.x. [DOI] [PubMed] [Google Scholar]
  10. Haynesworth S. E., Goshima J., Goldberg V. M., Caplan A. I. Characterization of cells with osteogenic potential from human marrow. Bone. 1992;13(1):81–88. doi: 10.1016/8756-3282(92)90364-3. [DOI] [PubMed] [Google Scholar]
  11. Jones S. J., Gray C., Sakamaki H., Arora M., Boyde A., Gourdie R., Green C. The incidence and size of gap junctions between the bone cells in rat calvaria. Anat Embryol (Berl) 1993 Apr;187(4):343–352. doi: 10.1007/BF00185892. [DOI] [PubMed] [Google Scholar]
  12. Krebsbach P. H., Kuznetsov S. A., Satomura K., Emmons R. V., Rowe D. W., Robey P. G. Bone formation in vivo: comparison of osteogenesis by transplanted mouse and human marrow stromal fibroblasts. Transplantation. 1997 Apr 27;63(8):1059–1069. doi: 10.1097/00007890-199704270-00003. [DOI] [PubMed] [Google Scholar]
  13. Kuznetsov S. A., Krebsbach P. H., Satomura K., Kerr J., Riminucci M., Benayahu D., Robey P. G. Single-colony derived strains of human marrow stromal fibroblasts form bone after transplantation in vivo. J Bone Miner Res. 1997 Sep;12(9):1335–1347. doi: 10.1359/jbmr.1997.12.9.1335. [DOI] [PubMed] [Google Scholar]
  14. Kuznetsov S., Gehron Robey P. Species differences in growth requirements for bone marrow stromal fibroblast colony formation In vitro. Calcif Tissue Int. 1996 Oct;59(4):265–270. doi: 10.1007/s002239900121. [DOI] [PubMed] [Google Scholar]
  15. Liens D., Delmas P. D., Meunier P. J. Long-term effects of intravenous pamidronate in fibrous dysplasia of bone. Lancet. 1994 Apr 16;343(8903):953–954. doi: 10.1016/s0140-6736(94)90069-8. [DOI] [PubMed] [Google Scholar]
  16. Malchoff C. D., Reardon G., MacGillivray D. C., Yamase H., Rogol A. D., Malchoff D. M. An unusual presentation of McCune-Albright syndrome confirmed by an activating mutation of the Gs alpha-subunit from a bone lesion. J Clin Endocrinol Metab. 1994 Mar;78(3):803–806. doi: 10.1210/jcem.78.3.8126161. [DOI] [PubMed] [Google Scholar]
  17. Marie P. J., de Pollak C., Chanson P., Lomri A. Increased proliferation of osteoblastic cells expressing the activating Gs alpha mutation in monostotic and polyostotic fibrous dysplasia. Am J Pathol. 1997 Mar;150(3):1059–1069. [PMC free article] [PubMed] [Google Scholar]
  18. Owen M., Friedenstein A. J. Stromal stem cells: marrow-derived osteogenic precursors. Ciba Found Symp. 1988;136:42–60. doi: 10.1002/9780470513637.ch4. [DOI] [PubMed] [Google Scholar]
  19. Owen M. Marrow stromal stem cells. J Cell Sci Suppl. 1988;10:63–76. doi: 10.1242/jcs.1988.supplement_10.5. [DOI] [PubMed] [Google Scholar]
  20. Riminucci M., Fisher L. W., Shenker A., Spiegel A. M., Bianco P., Gehron Robey P. Fibrous dysplasia of bone in the McCune-Albright syndrome: abnormalities in bone formation. Am J Pathol. 1997 Dec;151(6):1587–1600. [PMC free article] [PubMed] [Google Scholar]
  21. Schwindinger W. F., Francomano C. A., Levine M. A. Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):5152–5156. doi: 10.1073/pnas.89.11.5152. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Shenker A., Weinstein L. S., Moran A., Pescovitz O. H., Charest N. J., Boney C. M., Van Wyk J. J., Merino M. J., Feuillan P. P., Spiegel A. M. Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS. J Pediatr. 1993 Oct;123(4):509–518. doi: 10.1016/s0022-3476(05)80943-6. [DOI] [PubMed] [Google Scholar]
  23. Shenker A., Weinstein L. S., Sweet D. E., Spiegel A. M. An activating Gs alpha mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome. J Clin Endocrinol Metab. 1994 Sep;79(3):750–755. doi: 10.1210/jcem.79.3.8077356. [DOI] [PubMed] [Google Scholar]
  24. Spiegel A. M. The molecular basis of disorders caused by defects in G proteins. Horm Res. 1997;47(3):89–96. doi: 10.1159/000185441. [DOI] [PubMed] [Google Scholar]
  25. Wang H. Y., Malbon C. C. The Gs alpha/Gi alpha 2 axis controls adipogenesis independently of adenylylcyclase. Int J Obes Relat Metab Disord. 1996 Mar;20 (Suppl 3):S26–S31. [PubMed] [Google Scholar]
  26. Wang H. Y., Watkins D. C., Malbon C. C. Antisense oligodeoxynucleotides to GS protein alpha-subunit sequence accelerate differentiation of fibroblasts to adipocytes. Nature. 1992 Jul 23;358(6384):334–337. doi: 10.1038/358334a0. [DOI] [PubMed] [Google Scholar]
  27. Weinstein L. S., Shenker A., Gejman P. V., Merino M. J., Friedman E., Spiegel A. M. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med. 1991 Dec 12;325(24):1688–1695. doi: 10.1056/NEJM199112123252403. [DOI] [PubMed] [Google Scholar]
  28. Yamamoto T., Ozono K., Kasayama S., Yoh K., Hiroshima K., Takagi M., Matsumoto S., Michigami T., Yamaoka K., Kishimoto T. Increased IL-6-production by cells isolated from the fibrous bone dysplasia tissues in patients with McCune-Albright syndrome. J Clin Invest. 1996 Jul 1;98(1):30–35. doi: 10.1172/JCI118773. [DOI] [PMC free article] [PubMed] [Google Scholar]

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