Xd. Xi et al., DIFFERENTIAL-EFFECTS OF RECOMBINANT HUMAN INTERLEUKIN-13 ON THE IN-VITRO GROWTH OF HUMAN HEMATOPOIETIC PROGENITOR CELLS, British Journal of Haematology, 90(4), 1995, pp. 921-927
Effects of recombinant human interleukin (EL)-13 on in vitro haemopoie
sis from non-adherent mononuclear cells (NAMC) or highly enriched CD34
(+) cells of human cord blood (CB) were studied. IL-13 significantly i
ncreased megakaryocyte (MK) colony formation from either NAMC or CD34(
+) cells cultured in a plasma clot system supplemented with aplastic a
naemia serum (AAS) and phytohaemagglutinin-stimulated human peripheral
blood leucocyte-conditioned medium (PHA-LCM) in a dose-dependent mann
er. Experiments using a modified plasma clot culture, in which normal
AB serum and various cytokines were added to replace AAS and PHA-LCM,
demonstrated an increased MK colony number in the presence of IL-13, e
specially in combination with IL-3. However, IL-13 had no stimulatory
effect, but rather a slight inhibitory effect in some cases on granulo
cyte-macrophage (GM) colony formation in both plasma clot cultures. Fu
rthermore, the growth of GM progenitor cells in a methylcellulose cult
ure system in the presence of IL-3, GM-CSF, Epo, G-CSF or in combinati
on was significantly inhibited by the addition of IL-13. On the other
hand, high concentrations (100 ng/ml) of IL-13 were needed to cause a
slight inhibition on the growth of BFU-E-derived colonies under the sa
me methylcellulose culture. These results indicate that IL-13, alone a
nd synergistically with the effect of IL-3, promotes MK colony formati
on, but it inhibits the growth of GM and erythroid progenitor cells in
vitro.