par De Bruyn, Cécile 
;Delforge, Alain ;Bron, Dominique ;Bernier, M.;Massy, Martine;De Hemptinne, D.;Stryckmans, Pierre
Référence Journal of hematotherapy, 6, 2, page (93-102)
Publication Publié, 1997-04
;Delforge, Alain ;Bron, Dominique ;Bernier, M.;Massy, Martine;De Hemptinne, D.;Stryckmans, Pierre Référence Journal of hematotherapy, 6, 2, page (93-102)
Publication Publié, 1997-04
Article révisé par les pairs
| Résumé : | CD34+ cord blood (CB) cells were expanded in stromal cell-free long-term culture (LTC), in the presence of various combinations of interleukin-3 (IL-3), stem cell factor (SCF), IL-6, granulocyte-macrophage colony-stimulating factor (GM-CSF), and anti-transforming growth factor-beta (anti-TGF-beta) antibody. The progenitor cell expansion was evaluated by monitoring the increase of CD34+ and CD34 + CD38- cells over a period of 21 days. The expansion of immature (B1-CFC, HPP-CFC) and of more committed progenitors (CFU-GM, CFU-GEMM, BFU-E) was also evaluated in specific samples. Our results show that (a) CD34+ cell expansion is highly variable depending on the cord blood samples studied, (b) significant correlations between B1-CFC and CD34 + CD38- and between total CFU and CD34+ cell expansion are observed, (c) SCF in combination with IL-3 appears to expand cell subsets that continue to express their CD34 + CD38- phenotype and that generate both immature and committed progenitors, and (d) the addition of IL-6, GM-CSF, or anti-TGF-beta does not significantly improve these expansions. |
