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Optimizing Osteogenic Differentiation of Ovine Adipose-Derived Stem Cells by Osteogenic Induction Medium and FGFb, BMP2, or NELL1 In Vitro

机译:通过成骨诱导培养基和FGFb,BMP2或NELL1体外优化绵羊脂肪衍生干细胞的成骨分化

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Although adipose-derived stromal cells (ADSCs) have been a major focus as an alternative to autologous bone graft in orthopedic surgery, bone formation potential of ADSCs is not well known and cytokines as osteogenic inducers on ADSCs are being investigated. This study aimed at isolating ADSCs from ovine adipose tissue (AT) and optimizing osteogenic differentiation of ovine ADSCs (oADSC) by culture medium and growth factors. Four AT samples were harvested from two female ovine (Texel/Gotland breed), and oADSCs were isolated and analyzed by flow cytometry for surface markers CD29, CD44, CD31, and CD45. Osteogenic differentiation was made in vitro by seeding oADSCs in osteogenic induction medium (OIM) containing fibroblast growth factor basic (FGFb), bone morphogenetic protein 2 (BMP2), or NEL-like molecule 1 (NELL1) in 4 different dosages (1, 10, 50, and 100 ng/ml, respectively). Basic medium (DMEM) was used as control. Analysis was made after 14 days by Alizarin red staining (ARS) and quantification. This study successfully harvested AT from ovine and verified isolated cells for minimal criteria for adipose stromal cells which suggests a feasible method for isolation of oADSCs. OIM showed significantly higher ARS to basic medium, and FGFb 10 ng/ml revealed significantly higher ARS to OIM alone after 14 days.
机译:尽管在整形外科手术中脂肪来源的基质细胞(ADSCs)已成为自体骨移植的替代方法的主要焦点,但ADSCs的骨形成潜力尚不为人所知,并且正在研究作为ADSCs成骨诱导物的细胞因子。这项研究旨在从绵羊脂肪组织(AT)中分离ADSC,并通过培养基和生长因子优化绵羊ADSC(oADSC)的成骨分化。从两个雌性绵羊(特塞尔/哥德兰犬种)收获四个AT样品,并分离oADSCs并通过流式细胞仪分析其表面标记CD29,CD44,CD31和CD45。成骨细胞的分化是通过将oADSCs植入成骨诱导细胞培养基(OIM)中进行的,该成骨诱导培养基包含成纤维细胞生长因子碱性(FGFb),骨形态发生蛋白2(BMP2)或NEL样分子1(NELL1)4种不同剂量(1、10 ,分别为50和100µng / ml)。基本培养基(DMEM)用作对照。 14天后通过茜素红染色(ARS)和定量进行分析。这项研究成功地从绵羊中收获了AT,并验证了分离的细胞对于脂肪基质细胞的最低标准,这为分离oADSCs提供了一种可行的方法。 OIM显示对基本培养基的ARS明显更高,而FGFb10μng/ ml在14天后单独对OIM的ARS明显更高。

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