The use of platelet transfusion to ensure the recovery of thrombopoiesis in
patients constitutes high-cost support. The identification and cloning of
recombinant human thrombopoietin (TPO) and the development of efficient met
hods of purification of hematopoietic stem cells and progenitor cells have
ameliorated the development of strategies of ex vivo expansion of megakaryo
cyte (MK) progenitor cells and mature MKs. Synergistic combinations of cyto
kines including TPO, interleukin (IL)-1, IL-3, IL-11, stem cell factor, and
FLT-3 ligand induce the ex vivo expansion of colony-forming unit-MK progen
itors and MKs from cytokine-mobilized peripheral blood cells, bone marrow a
nd cord blood CD34(+) cells. Depending on the various culture conditions, i
e, combinations of growth factors, initial concentration of CD34+, serum or
serum-free cultures, and/or oxygen tensions, the expansion-fold of MKs and
their progenitor cells vary greatly. The clinical applications of the rein
fusion of ex vivo-generated MK cells have been investigated successfully in
cancer patients following high-dose chemotherapy. This review reports the
latest information concerning ex vivo expansion of MKs and the current stat
us of clinical trials. Int J Hematol. 2000;71:203-210 (C) 2000 The Japanese
Society of Hematology.