To investigate the effects of culture conditions on the maintenance of
metabolic functions of cultured hepatocytes, long-term hepatocyte cul
ture lasting 20 days was performed under two different culture conditi
ons, i.e. stationary cultures utilizing porous polymer (polyvinyl form
al (PVF) resin) as a substratum and conventional monolayer dish cultur
es without PVF. Metabolic activities specific to hepatocytes were eval
uated in terms of ammonia metabolism, urea synthesis, and albumin secr
etion. Concerning ammonia metabolic and urea synthetic activities, no
significant differences in maintenance of these activities were found
between the two culture conditions, and these activities rapidly decre
ased with the elapse of the culture period, especially during the earl
y stage of the experiments. However, after day 10, these activities in
the stationary cultures were maintained al a slightly more favorable
level than in the monolayer cultures. On the other hand, compared with
ammonia metabolism and urea synthesis, stable and well-maintained alb
umin secretion of hepatocytes (60% of the activity in day 1) was exhib
ited in the stationary culture experiments, despite that this particul
ar activity under the monolayer culture condition gradually reduced to
a very low level (5.7% of that on day 1) at the end of the culture. F
rom the morphological observations, hepatocytes immobilized in the PVF
resin revealed individual spherical shapes without forming multicellu
lar aggregation, and it was suggested that this characteristic structu
re contributed to good albumin secretion of hepatocytes. In conclusion
, the advantages of the hepatocyte culture technique utilizing PVF res
in over the conventional dish culture in maintaining some representati
ve metabolic function specific to hepatocytes were clarified.