Skip to main content
Log in

Construction of artificial epithelial tissues prepared from human normal fibroblasts and C9 cervical epithelial cancer cells carrying human papillomavirus type 18 genes

  • Published:
Biotechnology and Bioprocess Engineering Aims and scope Submit manuscript

Abstract

One cervical cancer cell line, C9, carrying human papillomavirus type 18 (HPV18) genes that is one of the major etiologic oncoviruses for cervical cancer was characterized. This cell line was further characterized for its capacity related to the epithelial cell proliferation, stratification and differentiation in reconstituted artificial epithelial tissue. Thein vitro construction of three dimensional artificial cervical epithelial tissue has been engineered using C9 epithelial cancer cells, human foreskin fibroblasts and a matrix made of type I collagen by organotypic culture of epithelial cells. The morphology of paraffin embedded artificial tissue was examined by histochemical staining. The artificial epithelial tissues were well developed having multilayer. However, the tissue morphology was similar to the cervical tissue having displasia induced by HPV infection. The characteristics of the artificial tissues were examined by determining the expression of specific marker proteins. In the C9 derived artificial tissues, the expression of EGF receptor, an epithelial proliferation marker proteins for stratum basale was observed up to the stratum spinosum. Another epithelial proliferation marker for stratum spinosum, cytokeratins 5/6/18, were observed well over the stratum spinosum. For the differentiation markers, the expression of involucrin and filaggrin were observed while the terminal differentiation marker, cytokeratins 10/13 were not detected at all. Therefore the reconstituted artificial epithelial tissues expressed the same types of differentiation marker proteins that are expressed in normal human cervical epithelial tissues but lacked the final differentiation capacity representing characteristics of C9 cell line as a cancer tissue derived cell line. Expression of HPV18 E6 oncoprotein was also observed in this artificial cervical epithelial tissue though the intensity of the staining was weak. Thus this artificial cervical epithelial tissue though the intensity of the staining was weak. Thus this artificial epithelial tissue could be used as a useful model system to examine the relationship between HPV-induced cervical oncogenesis and epithelial cell differentiation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Yuspa, S. H. (1994) The Pathogenesis of Squamous Cell Cancer: Lessons Learned from Studies of Skin Carcinogenesis.Cancer Research 54: 1178–1189.

    CAS  Google Scholar 

  2. Woodworth, C. D., S. Waggoner, W. Barnes, M. H. Stoler, and J. A. Dipaolo (1990) Human cervical and foreskin epithelial cells immortalized by human papillomavirus DNAs exhibit dysplastic differentiationin vitro.Cancer Research 50: 3709–3715.

    CAS  Google Scholar 

  3. Vambutas, A., T. P. Di Lorenzo, and B. M. Steinberg (1993) Laryngeal papilloma cells have high levels of epidermal growth factor receptor and respond to epidermal growth factor by a decrease in epithelial differentiation.Cancer Research 53: 910–914.

    CAS  Google Scholar 

  4. Edgington, S. M. (1994) A Novel Force In Biotech: Tissue Engineering.Bio/Technology 44: 38–44.

    Google Scholar 

  5. Wilkins, L. M. S. R. Watson, S. J. Prosky, S. F. Meunier, and N. L. Parenteau (1994) Development of a bilayerd living skin construct for clinical applications.Biotechnology and Bioengineering 43:747–756.

    Article  CAS  Google Scholar 

  6. Glaser, V. (1995) In vitro systems getting a close look by industry and FDA.Genetic Engineering News, April 15.

  7. McClure, J. S. (1995) Skinethic Laboratory Perfects Human Epidermal Cell Culture Technique.Genetic Engeneering News, April 15.

  8. Navsaria, H. A., S. R. Myers, I. M. Leigh, and I. A. Mckay (1995) Culturing skinin vitro for wound therapy.trends in Biotechnology 13(3): 91–100.

    Article  CAS  Google Scholar 

  9. Yamazaki, M. (1994) A novel method to prepare size-regulated spheroids composed of human dermal fibroblasts.Biotechnology and Bioengineering 44: 38–44.

    Article  CAS  Google Scholar 

  10. Halberstadt, C. R., R. Hardin, K. Bezverkov, D. Snyder, L. Allen, and L. Landeen (1994) The in vitro growth of a three dimensional human dermal replacement using a single-pass perfusion system.Biotechnology and Bioengineering 43: 740–746.

    Article  CAS  Google Scholar 

  11. Meyers, C., M. G. Frattini, J. B. Hudson, and L. A. Laimins (1992) Biosynthesis of human papillomavirus from continuous cell line upon epithelial differentiation.Science 257: 971–973.

    Article  CAS  Google Scholar 

  12. Bossens, M. (1992)In vitro infection of normal human keratinocytes by human papillomavirus type 1 followed by amplification of the virial genome in reconstructed epidermis.Journal of General Virology 73: 3269–3273.

    Article  CAS  Google Scholar 

  13. Pei, X. F., P. A. Gorman, and F. M. Watt (1991) Two strains of human keratinocytes transfected with HPV 16 DNA: comparison with the normal parental cell.Carcinogenesis 12(2): 277–284.

    Article  CAS  Google Scholar 

  14. Sterling, J., M. Stanley, G. Gatward, and T. Minson (1990) Production of human papillomavirus type 16 virions in a keratinocyte cell line.Journal of Virology 64(12): 6305–6307.

    CAS  Google Scholar 

  15. Kwon, D. H., Y. H. Lee, D. H. Lee, S. H., Cha, Y. K. Choe, S. H. Park, I. S. Choi, and T. W. Chung (1993) Detection of tumor-associated human paillomavirus infections usingin situ hybridization and polymerase chain reaction in Korean women cervices.The Journal of the Korean Society of Virology 23(1): 27–38.

    Google Scholar 

  16. Yang, E. K., J. H. Lee, T. B. Choe, and J. K. Park (1993) Development of dermal equivalent using mouse fibroblasts.The Korean Journal of Applied Microbiology and Biotechnology 4: 381–391.

    Google Scholar 

  17. Yang, E. K., D. H. Lee, S. N. Park, T. B. Choe, and J. K. Park (1997) Contraction behavior of collagen gel and fibroblasts activity in dermal equivalent model.Journal of Microbiology and Biotechnology 7(4): 267–271.

    Google Scholar 

  18. Fusenig, N. E. (1992) Cell interaction and epithelial differentiation. P. 26–56. In: R. Ian Freshney (ed.)Culture of Epithelial Cells Wiley-Liss, Inc., New York, NY.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sue Nie Park.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yang, E.K., Jin, S.W., Kang, B.T. et al. Construction of artificial epithelial tissues prepared from human normal fibroblasts and C9 cervical epithelial cancer cells carrying human papillomavirus type 18 genes. Biotechnol. Bioprocess Eng. 3, 1–5 (1998). https://doi.org/10.1007/BF02932474

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02932474

Key words

Navigation