Hepatic tissue engineering on 3-dimensional biodegradable polymers within a pulsatile flow bioreactor

Dig Surg. 2001;18(3):196-203. doi: 10.1159/000050129.

Abstract

Background: An optimal method for hepatocyte transplantation is not yet determined. With the principles of tissue engineering in vitro conditioning of hepatocytes on biodegradable polymer in a flow bioreactor before implantation forming spheroids may achieve increased cell mass and function to replace lost organ function in vivo.

Methods: Biodegradable poly-L-lactic (PLLA) polymer discs were seeded with rat hepatocytes in a concentration of 10 x 10(6) cells per ml and exposed to a medium flow of 24 ml/min for 1, 2, 4 and 6 days. The number and diameter of spheroidal aggregates was measured by phase-contrast microscopy. H&E histology was performed. Albumin production as hepatocyte specific function was determined by ELISA.

Results: Spheroids of viable hepatocytes of 50-200 microm in diameter were formed. Both the number and diameter of the spheroids increased during the first 2 days and then remained constant until day 6. Albumin production was maintained throughout the culture period.

Conclusion: Short (2- 3 days) pre-transplant conditioning of hepatocytes in a flow bioreactor on biodegradable PLLA resulted in formation of spheroids with a liver-like morphology and preserved specific metabolic function. Tissue engineered hepatocyte spheroids on polymer may represent a functionally active and easy transplantable neotissue and may serve as an in vivo substitute for lost liver function.

MeSH terms

  • Albumins / metabolism
  • Animals
  • Biocompatible Materials*
  • Biomedical Engineering / instrumentation
  • Biomedical Engineering / methods*
  • Bioreactors
  • Cell Transplantation / methods
  • Hepatocytes / metabolism
  • Hepatocytes / transplantation*
  • In Vitro Techniques
  • Lactic Acid / metabolism
  • Liver Transplantation
  • Polymers*
  • Pulsatile Flow
  • Rats
  • Rats, Inbred Lew
  • Spheroids, Cellular / metabolism
  • Spheroids, Cellular / transplantation*
  • Time Factors

Substances

  • Albumins
  • Biocompatible Materials
  • Polymers
  • Lactic Acid