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首页> 外文期刊>Advanced Biomedical Research >The effects of fibrin–icariin nanoparticle loaded in poly (lactic-co-glycolic) acid scaffold as a localized delivery system on chondrogenesis of human adipose-derived stem cells
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The effects of fibrin–icariin nanoparticle loaded in poly (lactic-co-glycolic) acid scaffold as a localized delivery system on chondrogenesis of human adipose-derived stem cells

机译:纤维蛋白 - 逐渐纳米粒子在聚(乳酸二乙醇酸)酸支架中的影响为人脂肪衍生干细胞软骨发生的局部递送系统

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Background:Nowadays, cartilage tissue engineering is the best candidate for regeneration of cartilage defects. This study evaluates the effect of fibrin/icariin (ICA) nanoparticles (F/I NPs) on chondrogenesis of stem cells.Materials and Methods:F/I NPs were characterized by Dynamic Light Scattering DLS. Poly (lactic-co-glycolic) acid (PLGA)-F/I NP scaffold was fabricated and assessed by scanning electron microscope. Human adipose-derived stem cells (hADSCs) were seeded on scaffold and induced for chondrogenesis. After 14 days, cell viability and gene expression were analyzed by the 3-(4, 5- dimethylthiazol-2yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. MTT assay and real-time polymerase chain reaction (RT-PCR).Results:The size and surface charge of F/I NP were about 28-30 nm and - 17, respectively. The average of pore size of PLGA and PLGA-fibrin/ICA was 230 and 340 μm, respectively. Cell viability of differentiated cells in P/F group was higher than others significantly (P ≤ 0.05). Furthermore, quantitative RT-PCR analysis demonstrated that ICA upregulated cartilaginous-specific gene expression. Furthermore, the results of the expression of type I collagen revealed that ICA downregulated this gene significantly (P 0.01).Conclusions:The results indicated that F/I NP could be a potential factor for chondrogenesis of stem cells and downregulation of fibrocartilage marker.
机译:背景:如今,软骨组织工程是软骨缺陷再生的最佳候选者。本研究评估纤维蛋白/ ica in(ICA)纳米颗粒(F / I NPS)对干细胞软骨发生的影响。材料和方法:F / I NPS通过动态光散射DLS表征。通过扫描电子显微镜制造和评估聚(乳酸 - 共乙醇酸)酸(PLGA)-F / I NP支架。人脂肪衍生的干细胞(HADSCs)在支架上接种并诱导软骨发生。 14天后,通过3-(4,5-二甲基噻唑-200L)-2,5-二苯基四唑溴铵(MTT)测定分析细胞活力和基因表达。 MTT测定和实时聚合酶链反应(RT-PCR)。结果:F / I NP的尺寸和表面电荷分别为约28-30nm和-17。 PLGA和PLGA-纤维蛋白/ ICA的孔径的平均分别为230和340μm。 P / F组中分化细胞的细胞活力显着高于其他细胞(P≤0.05)。此外,定量RT-PCR分析证明了ICA上调的软骨质特异性基因表达。此外,I型胶原蛋白表达的结果显示ICA显着下调该基因(P <0.01)。结论:结果表明F / I NP可能是干细胞软骨发生的潜在因素,以及纤维纤维化标记的下调。

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