Differentiation of bone marrow cells into cells that express liver-specific genes in vitro: implication of the Notch signals in differentiation

Biochem Biophys Res Commun. 2003 May 16;304(4):691-5. doi: 10.1016/s0006-291x(03)00637-5.

Abstract

Bone marrow (BM) stem cells have been shown to differentiate into liver cells. It remains difficult to sort and culture BM stem cells, and the gene expression of liver-specific proteins in these cells has not been fully investigated. We used a negative selective magnetic cell separation system to obtain stem cell-enriched BM cells. The cells obtained were cultured with hepatocytes or with hepatocyte growth factor (HGF), and the differentiation of BM cells into cells expressing liver-specific genes, hepatocyte nuclear factor (HNF) 1alpha, cytokeratin (CK) 8, alpha-fetoprotein (AFP), and albumin was investigated by the reverse transcription-polymerase chain reaction. We also investigated the gene expressions of Notch receptor-1 (Notch-1) and its ligand Jagged-1 in BM cell differentiation. Sorted BM cells showed positive for Sca-1 (Ataxin-1) by immunofluorescence staining. Fluorescence activated cell sorter analysis showed that 32.6% of sorted BM cells had a high level of expression of the hematopoietic stem cell marker CD90 (Thy-1). When cultured with hepatocytes, these cells expressed the liver-specific genes HNF1alpha and CK8 on culture day 3, AFP and albumin on culture day 7. When cultured with HGF (20ng/ml), the cells expressed HNF1alpha on day 3 and CK8 on day 7. Gene expressions of Notch-1 and Jagged-1 were detected in cultured BM cells on day 3. These results suggest that the negative selective magnetic cell separation system is useful for the rapid preparation of stem cell-enriched BM cells, and that the Notch signaling pathway plays a role in BM cell differentiation into a hepatocyte lineage in vitro.

MeSH terms

  • Animals
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / physiology*
  • Calcium-Binding Proteins
  • Cell Differentiation / physiology*
  • Cells, Cultured
  • Hepatocytes / cytology
  • Hepatocytes / physiology*
  • Immunomagnetic Separation
  • Intercellular Signaling Peptides and Proteins
  • Jagged-1 Protein
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Phenotype
  • Proteins / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Notch1
  • Receptors, Cell Surface*
  • Serrate-Jagged Proteins
  • Signal Transduction / physiology
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors*

Substances

  • Calcium-Binding Proteins
  • Intercellular Signaling Peptides and Proteins
  • Jag1 protein, rat
  • Jagged-1 Protein
  • Membrane Proteins
  • Notch1 protein, rat
  • Proteins
  • Receptor, Notch1
  • Receptors, Cell Surface
  • Serrate-Jagged Proteins
  • Trans-Activators
  • Transcription Factors