The Histological Study of the Interactions between Rabbit Decellularized Esophagus Scaffold and the Blastema Tissue Obtained from the Pinna of New Zealand White Rabbit

Document Type : Original Article (s)

Authors

1 Professor, Department of Biology, School of Science AND Cell and Molecular Research Group, Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran

2 Department of Biology, School of Science, Ferdowsi University of Mashhad, Mashhad, Iran

3 Associate Professor, Department of Biology, School of Science AND Cell and Molecular Research Group, Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran

4 Associate Professor, Department of Biology, School of Science, Ferdowsi University of Mashhad, Mashhad, Iran

5 Assistant Professor, Department of Biology, School of Science, Ferdowsi University of Mashhad, Mashhad, Iran

Abstract

Background: The extracellular matrix (ECM) is a key component during regeneration and maintenance of tissues and organs and has inductive effects on the behaviors of cells. The objective of this study was to investigate the interactions between rabbit's esophageal scaffold with blastema tissue cells obtained from the pinnas of New Zealand white rabbits. Blastema is a collection of undifferentiated cells that are able to propagate and differentiate in a manner similar to embryonic cells.Methods: In this experimental study, after removing the esophagus, physical and chemical decellularization methods including snap-freeze thaw and treatment with Triton X-100 and sodium dodecyl sulfate (SDS), as detergents, were performed. To prepare the blastema tissue, the pinnas of New Zealand white rabbits were punched and after 48 hours, the blastema tissue was obtained by a second punch. After washing, the scaffolds were assembled inside the blastema rings and cultured in Dulbecco's Modified Eagle's Medium (DMEM).Findings: Histological studies demonstrated that using snap-freeze thaw and then treatment with 1% Triton X-100 for 24 hours followed by 0.5% SDS for 48 hours was the best decellularization procedure for preparing scaffolds from rabbit's esophagus. Furthermore, adhesion and migration of blastema tissue cells to esophageal scaffold were observed after two weeks of culture.Conclusion: It can be concluded that the extracellular matrix of the decellularized esophagus can have inductive effects on the proliferation, migration and adhesion of the blastema tissue cells.

Keywords


  1. Saxena AK. Tissue engineering and regenerative medicine research perspectives for pediatric surgery. Pediatr Surg Int 2010; 26(6): 557-73.
  2. Badylak SF, Freytes DO, Gilbert TW. Extracellular matrix as a biological scaffold material: Structure and function. Acta Biomater 2009; 5(1): 1-13.
  3. Daley WP, Peters SB, Larsen M. Extracellular matrix dynamics in development and regenerative medicine. J Cell Sci 2008; 121(Pt 3): 255-64.
  4. Lutolf MP, Hubbell JA. Synthetic biomaterials as instructive extracellular microenvironments for morphogenesis in tissue engineering. Nat Biotechnol 2005; 23(1): 47-55.
  5. Hynes RO. The extracellular matrix: not just pretty fibrils. Science 2009; 326(5957): 1216-9.
  6. Yurchenco PD. Basement membranes: cell scaffoldings and signaling platforms. Cold Spring Harb Perspect Biol 2011; 3(2).
  7. Bhrany AD, Beckstead BL, Lang TC, Farwell DG, Giachelli CM, Ratner BD. Development of an esophagus acellular matrix tissue scaffold. Tissue Eng 2006; 12(2): 319-30.
  8. Rishniw M, Rodriguez P, Que J, Burke ZD, Tosh D, Chen H, et al. Molecular aspects of esophageal development. Ann N Y Acad Sci 2011; 1232: 309-15.
  9. Ozeki M, Narita Y, Kagami H, Ohmiya N, Itoh A, Hirooka Y, et al. Evaluation of decellularized esophagus as a scaffold for cultured esophageal epithelial cells. J Biomed Mater Res A 2006; 79(4): 771-8.
  10. Corcoran JP, Ferretti P. RA regulation of keratin expression and myogenesis suggests different ways of regenerating muscle in adult amphibian limbs. J Cell Sci 1999; 112 (Pt 9): 1385-94.
  11. Mahdavi Shahri N, Naseri F, Kheirabadi M, Babaie S, Sadeghie Shakib F, Azarniya M. The Ultra Structural Study of Blastema in Pinna Tissues of Rabbits with Transmission Electron Microscope. Journal of Biological Sciences 2008; 8: 993-1000.
  12. Mahmoudi Z, Moghaddam Matin M, Saeinasab M, Nakhaei-Rad S, Mirahmadi M, Mahdavi Shahri N, et al. Blastema cells derived from rabbit ear show stem cell characteristics. Journal of Cell and Molecular Research 2011; 3(1): 25-31.
  13. Beckstead BL, Pan S, Bhrany AD, Bratt-Leal AM, Ratner BD, Giachelli CM. Esophageal epithelial cell interaction with synthetic and natural scaffolds for tissue engineering. Biomaterials 2005; 26(31): 6217-28.
  14. Tan JY, Chua CK, Leong KF, Chian KS, Leong WS, Tan LP. Esophageal tissue engineering: an in-depth review on scaffold design. Biotechnol Bioeng 2012; 109(1): 1-15.
  15. Fujimoto N, Tajima S, Ishibashi A. Elastin peptides induce migration and terminal differentiation of cultured keratinocytes via 67 kDa elastin receptor in vitro: 67 kDa elastin receptor is expressed in the keratinocytes eliminating elastic materials in elastosis perforans serpiginosa. J Invest Dermatol 2000; 115(4): 633-9.
  16. Lindberg K, Badylak SF. Porcine small intestinal submucosa (SIS): a bioscaffold supporting in vitro primary human epidermal cell differentiation and synthesis of basement membrane proteins. Burns 2001; 27(3): 254-66.
  17. Friedl P, Hegerfeldt Y, Tusch M. Collective cell migration in morphogenesis and cancer. Int J Dev Biol 2004; 48(5-6): 441-50.