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Establishment of an ES cell-derived murine megakaryocytic cell line, MKD1, with features of primary megakaryocyte progenitors.

机译:具有原代巨核祖细胞特征的ES细胞源性鼠巨核细胞系MKD1的建立。

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摘要

Because of the scarcity of megakaryocytes in hematopoietic tissues, studying megakaryopoiesis heavily relies on the availability of appropriate cellular models. Here, we report the establishment of a new mouse embryonic stem (ES) cell-derived megakaryocytic cell line, MKD1. The cells are factor-dependent, their cell surface immunophenotype and gene expression profile closely resemble that of primary megakaryocyte progenitors (MkPs) and they further differentiate along the megakaryocyte lineage upon valproic acid treatment. At a functional level, we show that ablation of SCL expression, a transcription factor critical for MkP maturation, leads to gene expression alterations similar to that observed in primary, Scl-excised MkPs. Moreover, the cell line is amenable to biochemical and transcriptional analyses, as we report for GpVI, a direct target of SCL. Thus, the MKD1 cell line offers a pertinent experimental model to study the cellular and molecular mechanisms underlying MkP biology and more broadly megakaryopoiesis.
机译:由于造血组织中缺乏巨核细胞,因此研究巨核细胞很大程度上依赖于合适的细胞模型的可用性。在这里,我们报告建立新的小鼠胚胎干(ES)细胞来源的巨核细胞系MKD1。这些细胞是因子依赖性的,它们的细胞表面免疫表型和基因表达谱与原代巨核细胞祖细胞(MkPs)非常相似,并且在丙戊酸处理后沿巨核细胞谱系进一步分化。在功能水平上,我们显示消融SCL表达,MkP成熟的关键转录因子,导致基因表达改变,类似于在原发性Scl切除的MkPs中观察到的改变。此外,正如我们报告的Sp的直接靶点GpVI一样,该细胞系适合进行生化和转录分析。因此,MKD1细胞系提供了一个相关的实验模型来研究MkP生物学和更广泛的巨核细胞生成基础的细胞和分子机制。

著录项

  • 作者

    Chagraoui, H; Porcher, C;

  • 作者单位
  • 年度 2012
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  • 原文格式 PDF
  • 正文语种 eng
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