[Protocols for cloning human bone marrow-derived hepatic stem cells in vitro]

Nan Fang Yi Ke Da Xue Xue Bao. 2010 Feb;30(2):318-20.
[Article in Chinese]

Abstract

Objective: To explore practical protocols for cloning bone marrow-derived hepatic stem cells in vitro.

Methods: The cell fraction rich in CD117(+) cells and CD184(+) cells was separated from fresh bone marrow by density gradient centrifugation and cultured for 0, 7 and 14 days in high-glucose DMEM supplemented with or without 10% autologous serum or in serum-free high-glucose DMEM. All the media were supplemented with different concentrations of hepatocyte growth promoting factors (HGPF), thrombopoietin (TPO) and interleukin-3 (IL-3). The quantitative changes of CD117(+) cells and CD184(+) cells were measured by flow cytometry.

Results: The optimal effect for cell cloning was achieved with high-glucose DMEM with 10% autologous serum group supplemented with 40 microg/ml HGPF, 50 ng/ml TPO, and 10 ng/ml IL-3. At day 7 of cell culture in this media, the quantity of CD117(+) cells and CD184(+) cells increased by 6.55 and 6.20 folds, and by 11.62 and 20.57 folds at day 14, respectively.

Conclusion: It is practical for cloning bone marrow-derived hepatic stem cells in high-glucose DMEM with 10% autologous serum supplemented with 40 microg/ml HGPF, 50 ng/ml TPO, and 10 ng/ml IL-3.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Marrow Cells / cytology*
  • Cell Culture Techniques*
  • Clone Cells
  • Hepatocyte Growth Factor / pharmacology
  • Hepatocytes / cytology
  • Hepatocytes / physiology
  • Humans
  • Liver / cytology*
  • Proto-Oncogene Proteins c-kit / metabolism*
  • Stem Cells / cytology*
  • Thrombopoietin / pharmacology

Substances

  • Hepatocyte Growth Factor
  • Thrombopoietin
  • Proto-Oncogene Proteins c-kit