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首页> 外文期刊>Journal of chemotherapy >High dose chemotherapy and transplantation of hematopoietic progenitors from murine D3 embryonic stem cells.
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High dose chemotherapy and transplantation of hematopoietic progenitors from murine D3 embryonic stem cells.

机译:高剂量化学疗法和小鼠D3胚胎干细胞造血祖细胞的移植。

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摘要

Differentiating embryonic stem (ES) cells are an increasingly important source of hematopoietic progenitors, useful for both basic research and clinical applications. To date, characteristics of specific factors capable of influencing hematopoietic cell fate from ES cells remains elusive. We report that mMSC Feeder Layer and the combination of VEGF, SCF and TPO strongly promote hematopoietic differentiation. The results showed that the cells induced from ES-D3 expressed hematopoietic progenitor antigens (CD34 and CD117), myelocyte cell antigen (CD11b), erythrocyte cell antigen (Ter119), and transcription factors (Flk-1, GATA-2, SCL, beta-H1 and beta-major). Furthermore, those induced differentiated cells were injected into female C57BL/6 mice which were treated with high dose topotecan chemotherapy to restore part of their blood system function. We observed rapid white blood cell recovery, which suggested that the infusion of differentiated cells has a positive impact on hematopoiesis. The Sry gene in peripheral blood, bone marrow and spleen of transplanted female mice was confirmed by PCR analysis, which affirmed the existence of the chimera.
机译:分化胚胎干(ES)细胞是造血祖细胞的越来越重要的来源,可用于基础研究和临床应用。迄今为止,能够影响来自ES细胞的造血细胞命运的特定因子的特征仍然难以捉摸。我们报告说,mMSC饲养层以及VEGF,SCF和TPO的结合强烈促进造血分化。结果表明,ES-D3诱导的细胞表达造血祖细胞抗原(CD34和CD117),骨髓细胞抗原(CD11b),红细胞抗原(Ter119)和转录因子(Flk-1,GATA-2,SCL,β -H1和Beta-major)。此外,将那些诱导分化的细胞注射到雌性C57BL / 6小鼠中,用高剂量拓扑替康化疗对其进行治疗,以恢复其部分血液系统功能。我们观察到白细胞迅速恢复,这表明输注分化细胞对造血功能有积极影响。通过PCR分析证实了移植雌性小鼠外周血,骨髓和脾脏中的Sry基因,证实了嵌合体的存在。

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