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Directed Differentiation of Adult Liver Derived Mesenchymal Like Stem Cells into Functional Hepatocytes

机译:成人肝脏衍生间充质如干细胞的定向分化为功能性肝细胞

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Shortage of functional hepatocytes hampers drug safety testing and therapeutic applications because mature hepatocytes cannot be expanded and maintain functions in vitro. Recent studies have reported that liver progenitor cells can originate from mature hepatocytes in vivo. Derivation of proliferating progenitor cells from mature hepatocytes, and re-differentiation into functional hepatocytes in vitro has not been successful. Here we report the derivation of novel mesenchymal-like stem cells (arHMSCs) from adult rat hepatocytes. Immunofluorescence and flow cytometry characterization of arHMSCs found expression of mesenchymal markers CD29, CD44, CD90, vimentin and alpha smooth muscle actin. These arHMSCs proliferated in vitro for 4 passages yielding 104 fold increase in cell number in 28 days, and differentiated into hepatocyte-like cells (arHMSC-H). The arHMSC-H expressed significantly higher level of hepatocyte-specific markers (200 fold for albumin and 6 fold for Cyp450 enzymes) than arHMSCs. The arHMSC-H also demonstrated dose response curves similar to primary hepatocytes for 3 of the 6 paradigm hepatotoxicants tested, demonstrating utility in drug safety testing applications.
机译:功能性肝细胞的短缺妨碍药物安全测试和治疗应用,因为成熟的肝细胞不能在体外扩展和维持功能。最近的研究报道说,肝祖细胞可以源于体内成熟的肝细胞。从成熟肝细胞增殖祖细胞的衍生,并在体外重新分化为功能性肝细胞并未成功。在这里,我们报告了来自成年大鼠肝细胞的新型间充质样干细胞(ArhMSCs)的衍生。 ARHMSCS的免疫荧光和流式细胞术表征发现间充质标志物CD29,CD44,CD90,Vimentin和α平滑肌肌动蛋白的表达。这些arhmss在体外增殖4次通道,在28天内产生104倍的细胞数,并分化为肝细胞样细胞(Arhmsc-h)。 ARHMSC-H表达了比ARHMSCS显着更高水平的肝细胞特异性标记物(200倍,用于CYP450酶6倍)。 ARHMSC-H还证明了类似于6个范式肝毒剂中的3种初级肝细胞的剂量反应曲线,证明了药物安全测试应用中的效用。

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