Induction of proliferation and differentiation of cultured urothelial cells on acellular biomaterials

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Gouya Ram-Liebig - , Department of Urology (Author)
  • Axel Meye - , Department of Urology (Author)
  • Oliver W. Hakenberg - , Department of Urology (Author)
  • Michael Haase - , Institute of Pathology (Author)
  • Gustavo Baretton - , Institute of Pathology (Author)
  • Manfred P. Wirth - , Department of Urology (Author)

Abstract

OBJECTIVE: To determine the optimum conditions for the proliferation of urothelial cells, leading to the confluent coverage of large surfaces of biocompatible membranes, and for their terminal differentiation. MATERIALS AND METHODS: Porcine and human urothelial cells were cultured on different matrices under different growth conditions. Proliferative activity and the viability of cells were evaluated using fluorescent markers for nuclei and cytoplasm. Growth and differentiation were assessed by histological, histochemical and immunohistochemical methods. RESULTS: Under fibroblastic induction and supplementation of 5% fetal calf serum (FCS), urothelial cells showed more proliferation than in other conditions tested. Terminal differentiation of superficial cells was achieved by lowering the concentration of FCS to 1% at the air-liquid interface. CONCLUSIONS: The mitogenic effects of the extracellular matrix content of biological membranes and fibroblastic inductive factors are synergistic with each other, and can compensate for a low FCS concentration and the absence of other additives. Lowering the FCS concentration to 1% inhibits the proliferation of urothelial cells and permits their terminal differentiation.

Details

Original languageEnglish
Pages (from-to)922-927
Number of pages6
JournalBJU international
Volume94
Issue number6
Publication statusPublished - Oct 2004
Peer-reviewedYes

External IDs

PubMed 15476537

Keywords

ASJC Scopus subject areas

Keywords

  • Acellular matrix, Bladder, Cell culture, Urothelium