Dynamic organ culture is superior to multiwell plate culture for maintaining precision-cut tissue slices

Optimization of tissue slice culture, part 1

Robyn L. Fisher, Richard P. Shaughnessy, Patty M. Jenkins, Mauricio L. Austin, Gavin L. Roth, A Jay Gandolfi, Klaus Brendel

Research output: Contribution to journalArticle

53 Citations (Scopus)

Abstract

The increase in the use of precision-cut tissue slices for metabolism and toxicity studies has resulted in the development of various incubation systems and techniques for culturing the slices. This has led to inconsistencies in data obtained from different laboratories. For data to be comparable from one laboratory to another, reliable and consistent incubation systems must be used that will give the researcher the most optimal tissue slice viabilities. This study compares and contrasts the dynamic organ culture system (surface culture) and the multiwell plate culture system (submersion culture). Rat liver slices were produced using the Brendel/Vitron tissue slicer under oxygenated and ice-cold V-7 preservation solution. The slices (200 μm thick) were incubated in Waymouth's medium + 10% fetal calf serum (1.7 mL) containing either sodium bicarbonate or Hepes and gassed with either 95%5% O2/CO2 or 95%5% air/CO2. Slice viability was assessed at 6, 24, 48, and 72 h using ATP content, K+ retention, protein synthesis, alanine aminotransferase and lactate dehydrogenase leakage, and MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) reduction. 7-Ethoxycoumarin metabolism was also used to assess the xenobiotic metabolic activity of liver slices. The results indicated that the dynamic organ culture system maintained rat liver slices at a higher level of viability than the multiwell plate culture system and that Waymouth's medium gassed with 95% O2/5% CO2 was the best incubation condition for both systems. Thus, it is essential to optimize slice viability in order to obtain reliable data that will ultimately be used to predict what will be seen in humans.

Original languageEnglish (US)
Pages (from-to)99-113
Number of pages15
JournalToxicology Mechanisms and Methods
Volume5
Issue number2
DOIs
StatePublished - 1995

Fingerprint

Tissue culture
Organ Culture Techniques
Liver
Tissue
Metabolism
Rats
Tissue Survival
Sodium Bicarbonate
Ice
Immersion
Xenobiotics
Alanine Transaminase
L-Lactate Dehydrogenase
Toxicity
Adenosine Triphosphate
Air
Research Personnel
Serum
Proteins

Keywords

  • Optimal slice viability
  • Organ culture
  • Tissue slices

ASJC Scopus subject areas

  • Toxicology
  • Health, Toxicology and Mutagenesis

Cite this

Dynamic organ culture is superior to multiwell plate culture for maintaining precision-cut tissue slices : Optimization of tissue slice culture, part 1. / Fisher, Robyn L.; Shaughnessy, Richard P.; Jenkins, Patty M.; Austin, Mauricio L.; Roth, Gavin L.; Gandolfi, A Jay; Brendel, Klaus.

In: Toxicology Mechanisms and Methods, Vol. 5, No. 2, 1995, p. 99-113.

Research output: Contribution to journalArticle

Fisher, Robyn L. ; Shaughnessy, Richard P. ; Jenkins, Patty M. ; Austin, Mauricio L. ; Roth, Gavin L. ; Gandolfi, A Jay ; Brendel, Klaus. / Dynamic organ culture is superior to multiwell plate culture for maintaining precision-cut tissue slices : Optimization of tissue slice culture, part 1. In: Toxicology Mechanisms and Methods. 1995 ; Vol. 5, No. 2. pp. 99-113.
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