EFFECTS OF RECOMBINANT HUMAN THROMBOPOIETIN ALONE AND IN COMBINATION WITH ERYTHROPOIETIN AND EARLY-ACTING CYTOKINES ON HUMAN MOBILIZED PURIFIED CD34(-DEPLETED MEDIUM() PROGENITOR CELLS CULTURED IN SERUM)
J. Birkmann et al., EFFECTS OF RECOMBINANT HUMAN THROMBOPOIETIN ALONE AND IN COMBINATION WITH ERYTHROPOIETIN AND EARLY-ACTING CYTOKINES ON HUMAN MOBILIZED PURIFIED CD34(-DEPLETED MEDIUM() PROGENITOR CELLS CULTURED IN SERUM), Stem cells, 15(1), 1997, pp. 18-32
The effects of recombinant thrombopoietin (TPO) alone and in combinati
on with erythropoietin (EPO) and early-acting cytokines such as interl
eukin 3 (IL-3), stem cell factor (SCF) and GM-CSF on highly purified m
obilized human CD34(+) progenitor cells were studied in a serum-deplet
ed culture system, Eight leukapheresis samples were cultured for seven
days and analyzed; aliquots sere replated and re-evaluated on day 12.
Three-color bow cytometry was used together with morphologic analysis
to determine proliferation and megakaryocytic or erythroid maturation
, TPO alone was sufficient for cell survival and proliferation in seru
m-depleted medium, In the absence of other growth factors, almost all
CD34(+) cells differentiated along the megakaryocytic pathway within 1
2 days, Concomitantly, the progenitor cells gradually acquired the mor
phologic features of mature megakaryocytes. After exposure to TPO for
one week, 50% of the cells still expressed CD34; by day 12 the remaini
ng CD34(+) cells (11%) were all coexpressing CD41. TPO alone did not s
upport proliferation of glycophorin-A-positive cells. The addition of
TPO to early-acting cytokines (EPO, GM-CSP, SCF and/or IL-3) not only
increased the overall megakaryocyte expansion, but also generated a di
fferent maturation pattern of the CD41(+) megakaryocyte progenitors, I
t further doubled the number of erythroid cells and c-kit(+) cells in
the second week of culture. Interestingly, the overall number of CD34(
+) cells was increased about fivefold when TPO was added to the early-
acting cytokines, with a marked expansion of the CD34(+)/CD41(+) and C
D34(+)/CD117(+) subpopulations, TPO can augment the pool of committed
progenitors, thereby increasing the number of its own target cells and
the number of EPO-responsive cells, These properties make TPO an inte
resting cytokine for the ex vivo expansion of human progenitor cells.