Myeloid differentiation of human cord blood CD34+ cells during ex vivo expansion using thrombopoietin, flt3-ligand and/or granulocyte-colony stimulating factor

Br J Haematol. 1999 Jun;105(4):1034-40. doi: 10.1046/j.1365-2141.1999.01456.x.

Abstract

We investigated the phenotypic changes of human umbilical cord blood (CB) CD34+ cells during ex vivo expansion using thrombopoietin (TPO), flt3-ligand (FL), and/or granulocyte-colony stimulating factor (G-CSF). During ex vivo expansion of CD34+ cells isolated from human CB for up to 5 weeks, surface expression of molecules on the cultured cells including CD64 (Fc gammaRI), CD32 (Fc gammaRII), CD16 (Fc gammaRII), CD11b (MAC-1) and CD18 (beta2-integrin) was analysed by flow cytometry along with simultaneous measurement of apoptosis by 7-aminoactinomycin D staining method. CD64, CD32 and/or CD18 expressing cells appeared in the cultures both with and without the addition of G-CSF until the tenth day. However, without G-CSF, CD16+ fractions did not appear and CD11b+ fractions were not maintained. With G-CSF, the CD16+ or CD11b+ fractions appeared only from the second week. These results suggest that G-CSF is necessary for the late stage of myeloid maturation during which CD16 and CD11b are expressed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD34 / metabolism*
  • Cell Differentiation
  • Cells, Cultured
  • Fetal Blood / cytology
  • Flow Cytometry
  • Granulocyte Colony-Stimulating Factor / pharmacology*
  • Humans
  • Leukocytes, Mononuclear / cytology*
  • Membrane Proteins / pharmacology*
  • Phenotype
  • Thrombopoietin / pharmacology*

Substances

  • Antigens, CD34
  • Membrane Proteins
  • flt3 ligand protein
  • Granulocyte Colony-Stimulating Factor
  • Thrombopoietin