| Literature DB >> 11796924 |
Jeong-Hae Kie1, Woo-Ick Yang, Mi-Kyung Lee, Tae-Jung Kwon, Yoo-Hong Min, Hyun-Ok Kim, Hyo-Seop Ahn, Seock-Ah Im, Hyung-Lae Kim, Hae-Young Park, Kyung-Ha Ryu, Wha-Soon Chung, Myeong-Heon Shin, Yu-Jin Jung, So-Youn Woo, Hae-Kyung Park, Ju-Young Seoh.
Abstract
Thrombopoietin (TPO) is widely used for ex vivo expansion of hematopoietic stem cells. Previously, we have reported that TPO induces a characteristic pattern of apoptosis, and the TPO-induced apoptosis is closely associated with megakaryocyte (MK) differentiation. In the present study, several cytokines, flt3-ligand, stem cell factor (SCF), interleukin-3 (IL-3), IL-6, IL-11, leukemia inhibitory factor, G-CSF, and erythropoietin, which are known to affect megakaryocytopoiesis, have been evaluated to elucidate their effects on the TPO-induced apoptosis. Measurement of apoptosis by flow cytometry revealed that only SCF absolutely reduced the TPO-induced apoptosis in MK fractions, particularly in the late phase of ex vivo expansion. Platelet production was demonstrated by electron microscopy in a later phase when SCF was added. Simultaneous measurement of DNA contents with immunophenotyping demonstrated a significant increase in polyploidization in the CD41+ cell fraction when cultured with SCF. These results suggested that SCF not only inhibited premature senescence but also enhanced maturation of the differentiating cells of MK lineage during ex vivo expansion using TPO.Entities:
Mesh:
Substances:
Year: 2002 PMID: 11796924 DOI: 10.1634/stemcells.20-1-73
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277