CHARACTERIZATION OF A BIPOTENT ERYTHRO-MEGAKARYOCYTIC PROGENITOR IN HUMAN BONE-MARROW

The aim of the present study was to determine if the human erythroid ( E) and megakaryocytic (MK) lineages were closely linked to the existen ce of a bipotent burst-forming unit(BFU) E/MK progenitor. In methylcel lulose cultures, BFU-E/MK colonies were observed at day 12 and closely resembled mature BFU-E with the exception that the erythroid componen t was surrounded by MK. These colonies were quite different from the c olony forming unit (CFU)-GEMM-derived colonies, which were composed of a larger number of erythroblasts and which developed later in culture . The existence of these bilineage colonies composed of 100 to 1,000 e rythroblasts intermingled with a few MK and without granulocytic cells was confirmed by the plasma clot technique and immunoalkaline phospha tase labeling of the MK. To investigate if this bipotent progenitor be longed to the compartment of primitive progenitors, CD34(+) marrow cel ls were subfractionated according to expression of the CD38 antigen. T he bipotent BFU-E/MK progenitor as well as a large fraction of MK prog enitors were found in the CD34(+) CD38(+) or in the CD34(+) CD38(-) ce ll fractions. Growth of this bipotent BFU-E/MK progenitor required the combination of stem cell factor (SCF), interleukin-3 (IL-3), and Epo in serum free conditions. Addition of IL-6 had only a marginal effect, whereas megakaryocyte growth and development factor (MGDF) was not an absolute requirement, but slightly increased the plating efficiency o f CFU-MK and of BFU-E/MK progenitors when combined with SCF, IL-3, and Epo. In contrast, when these cultures were performed in the presence of 30% fetal calf serum, no BFU-E/MK colonies were observed irrespecti ve of the combination of growth factors used, including the presence o f MGDF; however, inclusion of the MS-5 cell line restored the growth o f this bipotent progenitor. In contrast, in cultures performed in the presence of human normal or aplastic plasma, MS-5 had only a slight ef fect on the cloning efficiency but improved MK cytoplasmic maturation and MK size, suggesting that the main effect of MS-5 is to diminish th e inhibitory effect of the fetal calf serum on the MK differ entiation . The clonal origin of bipotent BFU-E/MK colonies was demonstrated in liquid culture of single CD34(+) CD38(low) cells by immunophenotyping individual clones. At day 12, 30% of the clones contained erythroblast s (glycophorin A(+)) and some MK (CD41(+)) without granulocytes (G) or macrophages (M) (CD14(+) and CD15(+)). At day 20, clones containing e rythroblasts and MK were rare (546). In contrast multilineage clones c ould be frequently detected at this time without passage from BFU-E/MK clones at day 12 to GEMM at day 20. These results suggest that a bipo tent BFU-E/MK progenitor may be a nonrandom step in the hierarchical d evelopment of stem cells. 1996 by The American Society of Hematology.