首页> 外文期刊>Journal of Hepatology: The Journal of the European Association for the Study of the Liver >Differentiation of rat bone marrow cells cultured on artificial basement membrane containing extracellular matrix into a liver cell lineage.
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Differentiation of rat bone marrow cells cultured on artificial basement membrane containing extracellular matrix into a liver cell lineage.

机译:在含有细胞外基质的人工基底膜上培养的大鼠骨髓细胞分化为肝细胞谱系。

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BACKGROUND/AIMS: Bone marrow (BM) cells have been shown to be capable of differentiating into a liver cell lineage in vitro. However, their differentiation and proliferation is poor, and the cell characteristics are poorly understood. METHODS: We cultured rat BM cells on an artificial basement membrane containing extracellular matrix (ECM) with hepatocyte growth factor (HGF). The expression of mRNA for liver-specific genes was analyzed by reverse transcription PCR. The expression of albumin and Musashi-1 by cultured cells was analyzed using a fluorescence-activated cell sorter (FACS). The proportions of albumin-positive cells when culture was performed with different concentrations of HGF were analyzed by FACS. RESULTS: On culture day 21, polygonal cells proliferated and formed cell colonies. These cells expressed mRNA for all the liver-specific genes analyzed, and showed heterogeneous differentiation, some cells expressing albumin, others expressing Musashi-1. Albumin-positive differentiated cells were large and rich in intracellular structures, while Musashi-1-positive undifferentiated cells had the opposite characteristics. Culturing cells with higher concentrations of HGF induced an increased proportion of albumin-positive cells. CONCLUSIONS: The results suggest that cell culture on an ECM with a high concentration of HGF increases the extent to which BM cells differentiate into a liver cell lineage and proliferate in vitro.
机译:背景/目的:骨髓(BM)细胞已被证明能够在体外分化为肝细胞谱系。然而,它们的分化和增殖很差,并且对细胞的特性了解得很少。方法:我们在含有细胞外基质(ECM)和肝细胞生长因子(HGF)的人造基底膜上培养大鼠BM细胞。通过逆转录PCR分析肝特异性基因的mRNA表达。使用荧光激活细胞分选仪(FACS)分析培养细胞的白蛋白和Musashi-1的表达。通过FACS分析当用不同浓度的HGF进行培养时白蛋白阳性细胞的比例。结果:在培养第21天,多边形细胞增殖并形成细胞集落。这些细胞表达所有分析的肝脏特异性基因的mRNA,并表现出异质分化,一些细胞表达白蛋白,其他细胞表达Musashi-1。白蛋白阳性分化的细胞很大,细胞内结构丰富,而Musashi-1阳性未分化细胞则具有相反的特征。培养高浓度HGF的细胞诱导白蛋白阳性细胞比例增加。结论:结果表明,在高浓度HGF的ECM上进行细胞培养可增加BM细胞分化为肝细胞谱系并在体外增殖的程度。

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