Long-term culture of porcine bladder epithelial cells

Ursula K. Ehmann, Martha Kennedy Terris

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Epithelial cells from normal pig bladders proliferated when cocultured with lethally irradiated feeder cells of the LA7 rat mammary tumor line. When the bladder cells and feeders were plated together r at a confluent density, the bladder cells proliferated as the feeder cells died, resulting in a confluent culture of bladder cells. The bladder cells were successfully subcultured by plating with freshly irradiated LA7 feeder cells. In this way, bladder cells from five pigs were carried to confluency in passages 1, 4, 7, 7, and 13, amounting to at least 6, 18, 24, 26, and 45 doublings in culture, respectively, and none showed signs of slowed proliferation at the time of culture termination. Fibroblasts never became a prominent feature of these cultures, and their frequency was determined to be about 26 fibroblasts per 105 cells in passage 9. Pig bladder cells in 0,5% serum doubled in number in slightly over 3 d, whereas cells in 5,0% serum doubled in about 6 d. In fresh medium without feeder cells only minimal proliferation of bladder cells occurred. In LA7-conditioned medium the bladder cell numbers decreased, leading to the conclusion that the stimulus from LA7 cells is mechanically or physically transmitted. The bladder cells reacted with antibodies to keratins 7 and 18 but not to keratin 14 or vimentin. Tight junctions, visualized with an antibody to the ZO1 protein, connected all the cells to their neighbors. Most cells in passage 9 carried the diploid chromosome number of 38.

Original languageEnglish (US)
Article number3803137
Pages (from-to)137-141
Number of pages5
JournalIn Vitro Cellular and Developmental Biology - Animal
Volume38
Issue number3
DOIs
StatePublished - Jan 1 2002
Externally publishedYes

Fingerprint

Urinary Bladder
Swine
Epithelial Cells
Feeder Cells
Fibroblasts
Cell Count
Keratin-14
Keratin-7
Keratin-18
Antibodies
Tight Junctions
Vimentin
Conditioned Culture Medium
Serum
Diploidy
Cell Culture Techniques
Chromosomes
Cell Proliferation
Breast Neoplasms

Keywords

  • Bladder
  • Cell proliferation
  • Culture method
  • Feeder cells
  • Juxtacrine
  • Transitional epithelial cells

ASJC Scopus subject areas

  • Developmental Biology
  • Cell Biology

Cite this

Long-term culture of porcine bladder epithelial cells. / Ehmann, Ursula K.; Terris, Martha Kennedy.

In: In Vitro Cellular and Developmental Biology - Animal, Vol. 38, No. 3, 3803137, 01.01.2002, p. 137-141.

Research output: Contribution to journalArticle

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