Differentiation and maintenance of mast cells from CD34(+) human cord blood cells

Exp Hematol. 2006 Mar;34(3):320-9. doi: 10.1016/j.exphem.2005.12.007.

Abstract

Objective: Establishment of a stable umbilical cord blood CD34(+) (UCB CD34(+)) cell culture system and identification of the cells in the cobblestone area differentiated from UCB CD34(+) long-term culture cells.

Materials and methods: Human UCB CD34(+) cells were cultured on MS-5 mouse stroma cells in the presence of stem cell factor (SCF), flt-3 ligand (FL), and thrombopoietin (TPO) for 4 to 16 weeks. Cells in the culture medium and in the cobblestone area were collected and characterized by flow cytometry and microscopy.

Results: CD34(+) cells were stably expanded by culturing on MS-5 stroma cells in the presence of SCF, FL, and TPO for more than 4 months. Cells highly expressing CD117 (c-kit) appeared in the cobblestone area after 2 weeks and stably expanded. Isolation of cells highly expressing CD117 by fluorescence-activated cell sorter (FACS) revealed the cells were tryptase-positive and Fc epsilon receptor 1-negative mast cells. They showed typical mast cell morphology and released histamine upon stimulation by substance P or compound 48/80 in vitro.

Conclusion: Human UCB CD34(+) cells were stably expanded on MS-5 stroma cells in the presence of SCF, FL, and TPO. Under this condition, multipotent CD34(+) cells and mast cells differentiated from UCB CD34(+) cells were expanded in the cobblestone area. The expanded mast cells showed histamine release after substance P or compound 48/80 stimulation. These human mast cells will be useful as a source of human cells for evaluating the allergic effects of drugs.

MeSH terms

  • Animals
  • Antigens, CD34 / immunology*
  • Cell Differentiation*
  • Coculture Techniques
  • Fetal Blood / cytology*
  • Fetal Blood / immunology
  • Flow Cytometry
  • Humans
  • Immunophenotyping
  • Mast Cells / cytology*
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID

Substances

  • Antigens, CD34