首页> 外文期刊>Stem Cells >Decrease in apoptosis and increase in polyploidization of megakaryocytes by stem cell factor during ex vivo expansion of human cord blood CD34+ cells using thrombopoietin.
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Decrease in apoptosis and increase in polyploidization of megakaryocytes by stem cell factor during ex vivo expansion of human cord blood CD34+ cells using thrombopoietin.

机译:在使用血小板生成素对人脐带血 CD34+ 细胞进行体外扩增期间,干细胞因子减少巨核细胞凋亡和增加巨核细胞多倍体化。

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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.
机译:血小板生成素(TPO)广泛用于造血干细胞的离体扩增。此前,我们已经报道过TPO诱导细胞凋亡的特征性模式,并且TPO诱导的细胞凋亡与巨核细胞(MK)分化密切相关。在本研究中,已经评估了几种细胞因子,flt3 配体、干细胞因子 (SCF)、白细胞介素-3 (IL-3)、IL-6、IL-11、白血病抑制因子、G-CSF 和促红细胞生成素,这些细胞因子已知会影响巨核细胞生成,以阐明它们对 TPO 诱导的细胞凋亡的影响。通过流式细胞术测量细胞凋亡表明,只有 SCF 绝对减少了 TPO 诱导的 MK 组分凋亡,尤其是在离体扩增的后期。在添加SCF的后期阶段,通过电子显微镜证明了血小板的产生。同时测量具有免疫表型的 DNA 含量表明,当用 SCF 培养时,CD41+ 细胞组分的多倍体化显着增加。这些结果表明,SCF不仅抑制了过早衰老,而且在TPO的体外扩增过程中增强了MK谱系分化细胞的成熟。

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