PRIMARY CULTURE OF RAT HEPATOCYTES ENTRAPPED IN CYLINDRICAL COLLAGEN GELS - AN INVITRO SYSTEM WITH APPLICATION TO THE BIOARTIFICIAL LIVER -RAT HEPATOCYTES CULTURED IN CYLINDRICAL COLLAGEN GELS

Citation
Sl. Nyberg et al., PRIMARY CULTURE OF RAT HEPATOCYTES ENTRAPPED IN CYLINDRICAL COLLAGEN GELS - AN INVITRO SYSTEM WITH APPLICATION TO THE BIOARTIFICIAL LIVER -RAT HEPATOCYTES CULTURED IN CYLINDRICAL COLLAGEN GELS, Cytotechnology, 10(3), 1992, pp. 205-215
Citations number
46
Journal title
ISSN journal
09209069
Volume
10
Issue
3
Year of publication
1992
Pages
205 - 215
Database
ISI
SICI code
0920-9069(1992)10:3<205:PCORHE>2.0.ZU;2-Y
Abstract
A static culture model employing cylindrical collagen-hepatocyte gels is reported for large scale testing of conditions relevant to the thre e compartment hollow fiber bioartificial liver. High density hepatocyt e cultivation was achieved by cell entrapment within the collagen-hepa tocyte gel. Hepatocyte viability was assessed by vital staining, gel c ontraction, and insulin utilization. Measures of hepatocyte-specific f unction included albumin synthesis, ureagenesis, lidocaine biotransfor mation, and cholate conjugation. Although hepatocyte viability remaine d stable through the seven day incubation period, hepatocyte functions were not uniformly preserved. Albumin synthesis remained stable, whil e representative P-450 and conjugation activities decreased with time. This static culture system will facilitate the development of a hollo w fiber bioartificial liver which utilizes cylindrical collagen-hepato cyte gels.