Myeloid differentiation of human cord blood CD34(+) cells during ex vivo expansion using thrombopoietin, flt3-ligand and or granulocyte-colony stimulating factor
Es. Yoo et al., Myeloid differentiation of human cord blood CD34(+) cells during ex vivo expansion using thrombopoietin, flt3-ligand and or granulocyte-colony stimulating factor, BR J HAEM, 105(4), 1999, pp. 1034-1040
We investigated the phenotypic changes of human umbilical cord blood (CB) C
D34(+) cells during ex vivo expansion using thrombopoietin (TPO), flt3-liga
nd (FL), and/or granulocyte-colony stimulating factor (G-CSF). During ex vi
vo expansion of CD34(+) cells isolated from human CB for up to 5 weeks, sur
face expression of molecules on the cultured cells including CD64 (Fc gamma
RI), CD32 (Fc gamma RII), CD16 (Fc gamma RIII), CD11b (MAC-1) and CD18 (be
ta(2)-integrin) was analysed by flow cytometry along with simultaneous meas
urement of apoptosis by 7-aminoactinomycin D staining method. CD64, CD32, a
nd/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 myeloi
d maturation during which CD16 and CD11b are expressed.