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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >Protective effects of thrombopoietin and stem cell factor on X-irradiated CD34(+) megakaryocytic progenitor cells from human placental and umbilical cord blood
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Protective effects of thrombopoietin and stem cell factor on X-irradiated CD34(+) megakaryocytic progenitor cells from human placental and umbilical cord blood

机译:血小板生成素和干细胞因子对人胎盘和脐带血X射线照射的CD34(+)巨核祖细胞的保护作用

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In previous studies we characterized the radiosensitivity of CFU-megakaryocytes from human placental and umbilical cord blood and the effects of various early-acting cytokines. We found that the maximal clonal growth of CFU-megakaryocytes in vitro and maximal protection against X-ray damage were supported by a combination of thrombopoietin and stem cell factor. However, the mechanism by which the two cytokines exert a synergistic effect remained unclear, so we extended these studies to investigate the radioprotective action of synergistic thrombopoietin and stem cell factor on the survival of X-irradiated CD34(+) CFU-megakaryocytes. A combination of thrombopoietin and stem cell factor led to activation of mitogen-activated protein kinase and extracellular signal-regulated protein kinase and to suppression of caspase 3 in X-irradiated CD34+ cells. When PD98059 and various synthetic substrates-specific inhibitors of these proteins-were used, the combination had less effect on the clonal growth of X-irradiated CD34+ CFU-megakaryocytes. However, the addition of wortmannin, a specific inhibitor of the phosphatidylinositol-3 kinase pathway, did not alter the synergistic action of thrombopoietin plus stem cell factor. We suggest that part of this synergistic effect can be explained by activation of mitogen-activated protein kinase and extracellular signal-regulated protein kinase and by suppression of the caspase cascade. (C) 2003 by Radiation Research Society. [References: 25]
机译:在先前的研究中,我们表征了来自人胎盘和脐带血的CFU巨核细胞的放射敏感性以及各种早期作用的细胞因子的作用。我们发现血小板生成素和干细胞因子的组合支持体外CFU巨核细胞的最大克​​隆生长和对X射线损伤的最大保护。但是,这两种细胞因子发挥协同作用的机制尚不清楚,因此我们扩展了这些研究,以研究协同血小板生成素和干细胞因子对X射线照射的CD34(+)CFU巨核细胞存活的放射防护作用。血小板生成素和干细胞因子的组合导致活化有丝分裂原的蛋白激酶和细胞外信号调节的蛋白激酶,并抑制X射线照射的CD34 +细胞中的半胱天冬酶3。当使用PD98059和这些蛋白质的各种合成底物特异性抑制剂时,该组合对X射线辐射的CD34 + CFU巨核细胞的克隆生长影响较小。然而,加入渥曼青霉素,一种磷脂酰肌醇-3激酶途径的特异性抑制剂,并没有改变血小板生成素加干细胞因子的协同作用。我们建议这种协同作用的一部分可以通过丝裂原激活的蛋白激酶和细胞外信号调节的蛋白激酶的激活以及胱天蛋白酶级联的抑制来解释。 (C)2003年,辐射研究学会。 [参考:25]

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