Qualitative study of three cell culture methods

Aiguo Wang, Tao Xia, Peng Ran, Xuemin Chen, Andreas K. Nuessler

Current Medical Science ›› 2002, Vol. 22 ›› Issue (4) : 288-291.

Current Medical Science ›› 2002, Vol. 22 ›› Issue (4) : 288-291. DOI: 10.1007/BF02896766
Article

Qualitative study of three cell culture methods

Author information +
History +

Abstract

Primary rat hepatocytes were cultured using differentin vitro models and the enzyme leakage, albumin secretion, and cytochrome P450 1A (CYP 1A) activity were observed. The results showed that the level of LDH was decreased over time in culture. However, on day 5, LDH showed a significant increase in monolayer culture (MC) while after day 8 no LDH was detectable in sandwich culture (SC). The levels of AST and ALT did not change significantly over the investigated time. The CYP 1A activity was gradually decreased in a time-dependent manner in MC and SC. The decline of CYP 1A was faster in MC than in SC. This effect was partially reversed by using cytochrome P450 (CYP450) inducer such as Omeprazol and 3-methylcholanthrene (3-MC) and the CYP 1A induction was always higher in MC than in SC. In bioreactor basic CYP 1A activity was preserved over 2 weeks and the highest albumin production was observed in bioreactor followed by SC and MC. Taken together, it was indicated each investigated model had its advantages and disadvantages. It was also underlined that variousin vitro models may address different questions.

Keywords

monolayer culture / sandwich culture / bioreactor / enzyme leakage / albumin secretion / cytochrome P450 1A

Cite this article

Download citation ▾
Aiguo Wang, Tao Xia, Peng Ran, Xuemin Chen, Andreas K. Nuessler. Qualitative study of three cell culture methods. Current Medical Science, 2002, 22(4): 288‒291 https://doi.org/10.1007/BF02896766

References

[1]
SkettP. Problems in using isolated and cultured hepatocytes for xenobiotic metabolism/metabolism-based toxicity testing solution?. Toxic In vitro, 1994, 8: 491-491
CrossRef Google scholar
[2]
KernA, BaderA, PichlmayrR, et al. . Drug metabolism in hepatocyte sandwich cultures of rats and humans. Biochem Pharmacol, 1997, 54: 761-761
CrossRef Google scholar
[3]
GoethalsF, krackG, DeboyserD, et al. . Critical biochemical functions of isolated hepatocytes as sensitive indicators of chemical toxicity. Fundam Appl Toxicol, 1984, 4: 441-441
CrossRef Google scholar
[4]
SeglenP O. Preparation of isolated rat liver cells. Presscott DM Methods in Cell Biology, 1976, New York, Academic Press: 29-33
[5]
BrukeM D, MayerR T. Ethoxyresorufin: direct flourimetric assay of a microsomal O-dealkylation which is preferentially inducible by 3-methyl-cholanthrene. Drug Metab Dispos, 1974, 2: 583-583
[6]
NimsR W, LubetR A. Cytosol-mediated reduction of resorufin fluoresence: effects on the ethoxyresorufin O-deethylase (ETR) assay. Biochem Pharmacol, 1983, 32: 175-175
CrossRef Google scholar
[7]
YuK O, FisherJ W, BurtonG A, et al. . Carrier effects of dosing the H4IIE cells with 3,3′,4,4′-tetrachlorobiphenyl (PCB 77) in dimethyl sulfoxide or isooctane. Chemospere, 1997, 35: 895-895
CrossRef Google scholar
[8]
WeightonK, OttoI. Secretion of serum albumin by enzymatically isolated rat liver cells. FEBS-Lett, 1974, 46: 127-127
CrossRef Google scholar
[9]
Guguen-GuillouzoC, ClementB, BaffetG, et al. . Maintenance and reversibility of active albumin secretion by adult rat hepatocytes co-cultured with another liver epithelial cell type. Exp Cell Res, 1983, 143: 47-47
CrossRef Google scholar
[10]
DunnJ C, TompkinsR G, YarmushM L. Hepatocytes in collagen sandwich: evidence for transcriptional and translational regulation. J Cell Biol, 1992, 116: 1043-1043
CrossRef Google scholar

Accesses

Citations

Detail

Sections
Recommended

/