Liver-specific gene expression in cultured human hematopoietic stem cells

Stem Cells. 2003;21(1):98-104. doi: 10.1634/stemcells.21-1-98.

Abstract

Hematopoietic and hepatic stem cells share characteristic markers such as CD34, c-kit, and Thy1. Based on the recent observations that hepatocytes may originate from bone marrow, we investigated the potential of CD34(+) bone marrow cells to differentiate into hepatocytic cells in vitro. CD34(+) and CD34(-) human bone marrow cells were separated by magnetic cell sorting. Cells were cultured on a collagen matrix in a defined medium containing hepatocyte growth factor. Cell count and size were measured by flow cytometry, and reverse transcription polymerase chain reaction was carried out for the liver-specific markers CK-19 and albumin. During cell culture, CD34(+) cells showed an increasing cell number and proliferative activity as assessed by Ki-67 staining. Under the specified culture conditions, CD34(+) cells expressed albumin RNA and CK-19 RNA after 28 days, whereas CD34(-) cells did not show liver-specific gene expression. The results indicate that CD34(+) adult human bone marrow stem cells can differentiate into hepatocytic cells in vitro.

MeSH terms

  • Adult
  • Albumins / biosynthesis
  • Antigens, CD34 / biosynthesis
  • Bone Marrow
  • Bone Marrow Transplantation
  • Cell Count
  • Cell Differentiation / genetics
  • Cells, Cultured
  • Female
  • Flow Cytometry
  • Gene Expression Regulation / genetics*
  • Hematopoietic Stem Cells / chemistry*
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism*
  • Hepatocytes / chemistry
  • Hepatocytes / cytology
  • Hepatocytes / metabolism
  • Humans
  • Immunomagnetic Separation
  • Ki-67 Antigen / biosynthesis
  • Ki-67 Antigen / immunology
  • Liver / chemistry*
  • Liver / metabolism*
  • Male
  • Organ Specificity / genetics
  • RNA, Messenger / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cells / chemistry
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transplantation, Homologous

Substances

  • Albumins
  • Antigens, CD34
  • Ki-67 Antigen
  • RNA, Messenger