Stem cell factor protects c-kit(+) human primary erythroid cells from apoptosis

Objective. It has been reported that stem cell factor (SCF) promotes cell s urvival in primary cultured human erythroid colony-forming cells (ECFC), Gi ven the heterogeneous nature of ECFC, which may affect interpretation of th e data, we purified c-kit(+) ECFC and investigated the specificity and mech anisms of the anti-apoptotic effects of SCF on these cells. Materials and Methods. Glycophorin A(+) (GPA(+)) c-kit(+) cells were purifi ed from primary cultured ECFC derived from purified human CD34(+) cells. Th e GPA(+)c-kit(-) and nonerythroid cells were generated from the same CD34() cells. Apoptosis of ECFC was investigated in the absence or presence of S CF and erythropoietin (EPO) in serum-free medium. DNA fragmentation was mea sured with enzyme linked immunosorbent assay for oligonucleosome-sized DNA, gel electrophoresis, and annexin V labeling. Characterization of expanded cells and enriched cells was performed using multiparameter flow cytometry, For Akt assay, cells were lysed and the cleared lysates subjected to SDS-P AGE followed by Western blotting. Results. In GPA(+)c-kit(+) cells, deprivation of cytokine caused rapid DNA fragmentation within 4 hours that reached a maximum at 6 hours. This was pa rtially but clearly prevented by SCF or EPO, In contrast, no significant DN A fragmentation was seen in GPA(+)c-kit(-) and nonerythroid cells within 24 hours. PP2, a specific Src family kinase inhibitor, but not its inactive a nalogue PP3, reversed the anti-apoptotic effects of SCF, PP2 also inhibited SCF-induced phosphorylation of Akt, Conclusions. These data indicate that SCF protects purified human GPA(+)c-k it(+) cells from apoptosis and suggest that kit-mediated Src kinase activat ion is involved in Akt activation and cell survival. (C) 2001 International Society for Experimental Hematology. Published by Elsevier Science Inc.