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Improvement of C3A cell metabolism for usage in bioartificial liver support systems

  • C Filippi*
  • , SA Keatch
  • , D Rangar
  • , LJ Nelson
  • , PC Hayes
  • , JN Plevris
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Abstract

Background/Aims: The use of cell lines in bioartificial liver support systems (BALSS) to treat fulminant hepatic failure (FHF) is hindered by their reduced metabolic functions, which could be further decreased by the patient's serum/plasma. Hence, the aim of this study was to (i) test the effect of the FHF serum on C3A cell metabolism; (ii) precondition the cells to improve their metabolic capacity.

Methods: C3A cells were preconditioned in a medium developed at the University of Edinburgh (UoE) or a 10% FHF serum medium. Metabolism capacity was assessed on days 3,7 and 10 and compared with primary porcine hepatocytes. Preconditioned-cell metabolism was reassessed after (i) passage and (ii) incubation with 10% FHF serum.

Results: UoE-preconditioned cells showed time-dependent increase in gluconeogenesis (500%), ureogenesis (200%), galactose elimination (240%) albumin synthesis (250%). These results were in the same order of magnitude as the ones obtained with primary porcine hepatocytes and were further enhanced by cell passage. UoE-preconditioning prevented the decrease of metabolism induced by acute incubation with FHF serum on control C3A cells. Preconditioning with FHF serum did not improve cell metabolism.

Conclusions: Cell preconditioning with UoE-medium increases metabolic capacity and would greatly improve BALSS efficacy. (C) 2004 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Original languageEnglish
Pages (from-to)599-605
Number of pages7
JournalJournal of Hepatology
Volume41
Issue number4
DOIs
Publication statusPublished - Oct 2004

Keywords / Materials (for Non-textual outputs)

  • bioartificial liver support system
  • fulminant hepatic failure
  • ureogenesis
  • gluconeogenesis
  • albumin
  • galactose elimination
  • FULMINANT HEPATIC-FAILURE
  • ASSIST DEVICE
  • PROINFLAMMATORY CYTOKINES
  • HEPATOCYTES
  • LACTATE
  • TRANSPLANTATION
  • COCULTURE
  • CAPACITY
  • TRIAL
  • PIG

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