Serum-free, long-term cultures of human hepatocytes: maintenance of cell morphology, transcription factors, and liver-specific functions

Biochem Biophys Res Commun. 2000 Mar 5;269(1):46-53. doi: 10.1006/bbrc.2000.2215.

Abstract

Since human hepatocytes are available only in limited number, the development of a serum-free culture system for long-term cultivation of differentiated 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 epithelial and bile duct cells, cytokeratin (CK) 18 and 19, and liver-specific proteins, like phosphoenolpyruvate carboxykinase-2 (PCK2) and serum proteins, were expressed. Liver-enriched transcription factors CCAAT/enhancer binding protein alpha (C/EBPalpha) and hepatocyte nuclear factor-4 (HNF-4), cytokine and mitogen activated factors (nuclear factor kappa B) NFkappaB, and activator protein-1 (AP-1) were maintained and active for several weeks in our cultures. In summary, our serum-free culture system allows the culture of differentiated human hepatocytes for several weeks. It may serve as a model system for metabolic, pharmacologic-toxicologic studies, and studies on human pathogens under defined chemical conditions.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Blood Proteins / genetics
  • Blood Proteins / metabolism
  • Cell Culture Techniques / methods
  • Cell Differentiation
  • Cells, Cultured
  • Culture Media, Serum-Free
  • Gene Expression
  • Humans
  • Liver / cytology*
  • Liver / metabolism
  • Liver / physiology*
  • Microscopy, Electron
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Blood Proteins
  • Culture Media, Serum-Free
  • RNA, Messenger
  • Transcription Factors