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
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
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.