Bulletin of Experimental Biology and Medicine

, Volume 142, Issue 2, pp 250–253 | Cite as

Restoration of gastrocnemius muscle in mdx mice of different age after injury and implantation of xenogenic muscle tissue

  • V. N. Yarygin
  • M. A. Stenina
  • N. V. Bulyakova
  • V. S. Azarova
  • L. I. Krivov
  • V. I. Savchuk
  • Zh. V. Rudkovskaya
  • V. F. Sitnikov
Morphology and Pathomorphology
  • 41 Downloads

Abstract

The intensity of regeneration of crossed gastrocnemius muscle was evaluated in two groups of mdx mice of different age 2 weeks after implantation of crushed muscle tissue from newborn rats into the wound defect area. The effect of xenoplasty manifested in increased weight of the damaged muscle. The effect was observed in mice aging 12–16 weeks but not in those aged 40–48-weeks. Structural changes in the skeletal muscle tissue intrinsic of mdx mice and augmenting with age were detected in intact mice before the experiment. Activity of muscle fiber regeneration in intact and injured muscle of 40–48-week-old mice was significantly lower than in 12–16-week-old ones. Myoblasts of the xenogenic transplant retained viability in recipient muscles for at least 2 weeks. Post-traumatic regeneration was stimulated in only 12–16-week animals. Xenoplasty was ineffective in older animals and even somewhat enhanced the destructive processes in the muscle. It seems that age-specific regeneration activity of the recipient skeletal muscle tissue should be taken into consideration in the development of effective strategy of cell therapy for progressive muscular dystrophy.

Key Words

regeneration age cell technologies tissue therapy mdx mice 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    N. V. Bulyakova, M. F. Popova, S. M. Zubkova, et al., Laser and Tissue Therapy [in Russian], Moscow (1993).Google Scholar
  2. 2.
    M. F. Popova, Radiosensitivity and Stimulating Properties of Mammalian Regenerating Tissues [in Russian], Moscow (1984).Google Scholar
  3. 3.
    A. N. Studitskii and Z. P. Ignatyeva, Muscle Repair in Higher Mammals [in Russian], Moscow (1961).Google Scholar
  4. 4.
    J. E. Anderson and W. K. Ovalle, Anat. Res., 219, No. 3, 243–257 (1987).CrossRefGoogle Scholar
  5. 5.
    D. L. Bourke, M. Ontell, and F. Taylor, Am. J. Anat., 181, 1–11 (1988).PubMedCrossRefGoogle Scholar
  6. 6.
    A. E. Hellmuth and D. B. Allbrook, J. Anat., 110, No. 3, 503 (1971).PubMedGoogle Scholar
  7. 7.
    T. Kagawa, E. Chikata, J. Tani, et al., Develop. Biol., 65, No. 2, 526–530 (1978).PubMedCrossRefGoogle Scholar
  8. 8.
    S. S. Jejuricar and W. M. Kuzon Jr., Apoptosis, 8, No. 6, 573–578 (2003).CrossRefGoogle Scholar
  9. 9.
    I. Kinoshita, J. T. Vilquin, and J. P. Tremblay, Acta Neuropathol., 91, No. 5, 489–493 (1996).PubMedCrossRefGoogle Scholar
  10. 10.
    P. K. Law, T. G. Goodwin, Q. Fang, et al., Acta Paediatr. Jpn., 33, No. 2, 206–215 (1991).PubMedGoogle Scholar
  11. 11.
    M. Ontell, K. C. Feng, K. Klueber, et al., Anat. Rec., 208, 159–174 (1984).PubMedCrossRefGoogle Scholar
  12. 12.
    B. J. Petrof, J. B. Shrager, H. H. Stedman, et al. Proc. Natl. Acad. Sci. USA, 90, No. 8, 3710–3714 (1993).PubMedCrossRefGoogle Scholar
  13. 13.
    S. S. Shishkin, S. M. Terekhov, T. B. Krokhina, et al. Genetika, 37, No. 8, 1104–1111 (2001).PubMedGoogle Scholar
  14. 14.
    D. J. Watt, K. Lambert, J. E. Morgan, et al., J. Neurol. Sci., 57, 319–331 (1978).CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, Inc. 2006

Authors and Affiliations

  • V. N. Yarygin
    • 1
  • M. A. Stenina
    • 1
  • N. V. Bulyakova
    • 2
  • V. S. Azarova
    • 2
  • L. I. Krivov
    • 1
  • V. I. Savchuk
    • 1
  • Zh. V. Rudkovskaya
    • 1
  • V. F. Sitnikov
    • 1
  1. 1.Russian State Medical UniversityRussia
  2. 2.A. N. Severtsev Institute of Ecology and Evolution ProblemsRussian Academy of SciencesMoscow

Personalised recommendations