Differentiation of rat bone marrow cells cultured on artificial basement membrane containing extracellular matrix into a liver cell lineage

J Hepatol. 2005 Jul;43(1):110-6. doi: 10.1016/j.jhep.2005.01.037. Epub 2005 Apr 22.

Abstract

Background/aims: Bone marrow (BM) cells have been shown to be capable of differentiating into a liver cell lineage in vitro. However, their differentiation and proliferation is poor, and the cell characteristics are poorly understood.

Methods: We cultured rat BM cells on an artificial basement membrane containing extracellular matrix (ECM) with hepatocyte growth factor (HGF). The expression of mRNA for liver-specific genes was analyzed by reverse transcription PCR. The expression of albumin and Musashi-1 by cultured cells was analyzed using a fluorescence-activated cell sorter (FACS). The proportions of albumin-positive cells when culture was performed with different concentrations of HGF were analyzed by FACS.

Results: On culture day 21, polygonal cells proliferated and formed cell colonies. These cells expressed mRNA for all the liver-specific genes analyzed, and showed heterogeneous differentiation, some cells expressing albumin, others expressing Musashi-1. Albumin-positive differentiated cells were large and rich in intracellular structures, while Musashi-1-positive undifferentiated cells had the opposite characteristics. Culturing cells with higher concentrations of HGF induced an increased proportion of albumin-positive cells.

Conclusions: The results suggest that cell culture on an ECM with a high concentration of HGF increases the extent to which BM cells differentiate into a liver cell lineage and proliferate in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / metabolism
  • Animals
  • Basement Membrane*
  • Biomarkers / metabolism
  • Bone Marrow Cells / cytology*
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / physiology
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Division
  • Cell Lineage
  • Cell Separation
  • Cells, Cultured
  • Extracellular Matrix / physiology*
  • Flow Cytometry
  • Gene Expression
  • Hepatocyte Growth Factor / administration & dosage
  • Hepatocyte Growth Factor / pharmacology
  • Liver / cytology*
  • Liver / metabolism
  • Liver / physiology
  • Male
  • Membranes, Artificial*
  • Nerve Tissue Proteins / metabolism
  • Osmolar Concentration
  • RNA-Binding Proteins / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Albumins
  • Biomarkers
  • Membranes, Artificial
  • Msi1 protein, rat
  • Nerve Tissue Proteins
  • RNA-Binding Proteins
  • Hepatocyte Growth Factor