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Original Article

Spontaneous Occurrence of Anti-Fibrillin-1 Autoantibodies in Tight-Skin Mice

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Pages 151-155 | Received 17 Nov 1997, Published online: 07 Jul 2009

References

  • Jimenez S. A., Williams C. J., Meyers J. C., Bashey R. Increased collagen biosynthesis and increased expression of type I and type III procollagen genes in tight-skin (TSK) mouse fibroblasts. J. Biol. Chem. 1986; 261: 657–62
  • Hatakeyama A., Kasturi K. N., Wolf I., Phelps R. G., Bona C. A. Correlation between the concentration of serum antitopoisomerase I autoantibodies and histological and biochemical alterations in the skin of TSK mice. Cell Immunol. 1996; 167: 135–40
  • Osborn T. G., Bauer N. E., Ross S. C. The tight-skin mouse: physical and biochemical properties of the skin. J. Rheumatol. 1983; 10: 793–6
  • Osborn T. G., Bashey R. I., Moore T. L., Fischer V. W. Collagenous abnormalities in the heart of tight-skin mouse. J. Mol. Cell Cardiol. 1987; 19: 581–7
  • Bona C. A., Rothfield N. Autoantibodies in scleroderma and tight-skin mice. Curr. Opinion Immunol. 1994; 6: 931–7
  • Kasturi K. N., Muryoi T., Shibata S., et al. Functional and molecular characteristics of autoantibodies associated with tight-skin syndrome. New York Acad. Sci. 1996; 815: 253–62
  • Delustro F. A., Mackel A. M., LeRoy E. C. Delayed-type hypersensitivity of elastase soluble lung peptides in the tight-skin mouse. Cell Immunol. 1983; 81: 175–9
  • Green M. C., Sweet H. O., Bunker L. E. Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton. Am. J. Pathol. 1976; 82: 493–512
  • Siracusa L. D., McGrath R., Ma Q., et al. A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation. Genomic Res. 1996; 6: 300–13
  • Li X., Periera L., Zhang H., et al. Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosome 2 and 18. Genomics 1993; 18: 667–72
  • Kasturi K. N., Hatakeyama A., Murai C., Gordon R., Phelps R. G., Bona C. A. B cell deficient mice inheriting defective fibrillin-1 gene develop cutaneous hyperplasia. J. Autoimmun. 1997; 9: 473–83
  • Zhang H., Apfelroth S. D., Hu W., et al. Structure and expression of fibrillin 2, a novel microfibrillar component preferentially located in elastic matrices. J. Cell Biol. 1994; 124: 855–63
  • Yin W., Smiley E., Germiller J., et al. Primary structure and developmental expression of Fbn-1, the mouse fibrillin gene. J. Biol. Chem. 1995; 270: 1798–806
  • Raghunath M., Bachi T., Meuli M., et al. Fibrillin and elastin expression in skin regenerating from cultured keratinocyte autografts: Morphogenesis of microfibrils begins at the dermal-epidermal junction and precedes elastic fiber formation. J. Invest. Dermatol. 1996; 106: 1090–5
  • Phelps R. G., Daian C, Shinobu S., Fleischmajer R., Bona C. A. Induction of skin fibrosis and autoantibodies by infusion of immunocompetent cells from tight-skin mice into pa/pa mice. J. Autoimmun. 1993; 6: 701–18
  • Akita M., Lee S. H., Keneko K. Electron microscopic observations of elastic fibres in the lung and aorta in beta amino propio nitrate fed tight-skin mice. Histol. Histopathol. 1982; 7: 39–45
  • Gardi C., Martorana P. A., De Santi M. M., Even P. V., Lungarella G. A biochemical and morphological investigation of the early development of genetic emphysema in tight-skin mice. Exp. Mol. Pathol. 1989; 50: 398–410
  • Fleischmajer R., Jacob L., Schwartz E., Sakai L. Y. Extracellular microfibrils are increased in localized and systemic scleroderma skin. Lab. Invest. 1991; 64: 791–8

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