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首页> 外文期刊>Differentiation: The Journal of the International Society of Differentiation >Induced endothelial differentiation of cells from a murine embryonic mesenchymal cell line C3H/10T1/2 by angiogenic factors in vitro.
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Induced endothelial differentiation of cells from a murine embryonic mesenchymal cell line C3H/10T1/2 by angiogenic factors in vitro.

机译:体外通过血管生成因子诱导鼠胚胎间充质细胞系C3H / 10T1 / 2诱导的内皮细胞分化。

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A murine embryonic mesenchymal cell line C3H/10T1/2 possesses the potential to differentiate into multiple cell phenotypes and has been recognized as multipotent mesenchymal stem cells, but no in vitro model of its endothelial differentiation has been established and the effect of angiogenic factors on the differentiation is unknown. The aim of the present study was to evaluate the role of angiogenic factors in inducing endothelial differentiation of C3H/10T1/2 cells in vitro. C3H/10T1/2 cells were treated with angiogenic factors, VEGF (10 ng/mL) and bFGF (5 ng/mL). At specified time points, cells were subjected to morphological study, immunofluorescence staining, RT-PCR, LDL-uptake tests and 3-D culture for the examination of the structural and functional characteristics of endothelial cells. Classic cobblestone-like growth pattern appeared at 6 day of the induced differentiation. Immunofluorescence staining and RT-PCR analyses revealed that the induced cells exhibited endothelial cell-specific markers such as CD31, von Willebrand factor, Flk1, Flt1, VE-cadherin, Tie2, EphrinB2 and Vezf1 at 9 day. The induced C3H/10T1/2 cells exhibited functional characteristics of the mature endothelial phenotype, such as uptake of acetylated low-density lipoproteins (Ac-LDL) and formation of capillary-like structures in three-dimensional culture. At 9 day, Weibel-Palade bodies were observed under a transmission electron microscope. This study demonstrates, for the first time, endothelial differentiation of C3H/10T1/2 cells induced by angiogenic factors, VEGF and bFGF, and confirms the multipotential differentiation ability. This in vitro model is useful for investigating the molecular events in endothelial differentiation of mesenchymal stem cells.
机译:鼠胚胎间充质细胞系C3H / 10T1 / 2具有分化为多种细胞表型的潜力,并已被认为是多能性间充质干细胞,但尚未建立其内皮细胞分化的体外模型,并且血管生成因子对内皮细胞的影响分化是未知的。本研究的目的是评估血管生成因子在体外诱导C3H / 10T1 / 2细胞内皮分化中的作用。用血管生成因子,VEGF(10 ng / mL)和bFGF(5 ng / mL)处理C3H / 10T1 / 2细胞。在指定的时间点,对细胞进行形态学研究,免疫荧光染色,RT-PCR,LDL摄取测试和3-D培养,以检查内皮细胞的结构和功能特性。在诱导分化的第6天出现了经典的鹅卵石状生长模式。免疫荧光染色和RT-PCR分析表明,诱导的细胞在第9天显示出CD31,von Willebrand因子,Flk1,Flt1,VE-cadherin,Tie2,EphrinB2和Vezf1等内皮细胞特异性标记。诱导的C3H / 10T1 / 2细胞表现出成熟的内皮表型的功能特征,例如在三维培养中摄取乙酰化的低密度脂蛋白(Ac-LDL)和形成毛细管样结构。在第9天,在透射电子显微镜下观察了Weibel-Palade尸体。这项研究首次证明了由血管生成因子,VEGF和bFGF诱导的C3H / 10T1 / 2细胞的内皮细胞分化,并证实了其多能分化能力。该体外模型可用于研究间充质干细胞内皮分化中的分子事件。

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