D. Runge et al., Serum-free, long-term cultures of human hepatocytes: Maintenance of cell morphology, transcription factors, and liver-specific functions, BIOC BIOP R, 269(1), 2000, pp. 46-53
Citations number
45
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Since human hepatocytes are available only in Limited number, the developme
nt of a serum-free culture system for long-term cultivation of differentiat
ed and functional hepatocytes is of great importance. Here we describe the
culture of human hepatocytes in a chemically defined serum-free medium for
up to 5 weeks. Cell morphology was assayed by light and electron microscopy
and revealed a well-preserved cellular morphology. Marker proteins for epi
thelial and bile duct cells, cytokeratin (CK) 18 and 19, and liver-specific
proteins, Like phosphoenolpyruvate carboxykinase-2 (PCK2) and serum protei
ns, were expressed. fiver-enriched transcription factors CCAAT/enhancer bin
ding protein alpha (C/EBP alpha) and hepatocyte nuclear factor-4 (HNF-4), c
ytokine and mitogen activated factors (nuclear factor kappa B) NF kappa B,
and, activator protein-1 (AP-1) were maintained and active for several week
s in our cultures. In summary, our serum-free culture system allows the cul
ture of differentiated human hepatocytes for several weeks. It may serve as
a model system for metabolic, pharmacologic-toxicologic studies, and studi
es on human pathogens under defined chemical conditions. (C) 2000 Academic
Press.