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Chemical modification of extracellular matrix by cold atmospheric plasma-generated reactive species affects chondrogenesis and bone formation

机译:冷空气等离子体产生的反应性物质对细胞外基质的化学修饰影响软骨形成和骨形成

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摘要

The goal of this study was to investigate whether cold plasma generated by dielectric barrier discharge (DBD) modifies extracellular matrices (ECM) to influence chondrogenesis and endochondral ossification. Replacement of cartilage by bone during endochondral ossification is essential in fetal skeletal development, bone growth and fracture healing. Regulation of this process by the ECM occurs through matrix remodelling, involving a variety of cell attachment molecules and growth factors, which influence cell morphology and protein expression. The commercially available ECM, Matrigel, was treated with microsecond or nanosecond pulsed (µsp or nsp, respectively) DBD frequencies conditions at the equivalent frequencies (1 kHz) or power (~1 W). Recombinant human bone morphogenetic protein-2 was added and the mixture subcutaneously injected into mice to simulate ectopic endochondral ossification. Two weeks later, the masses were extracted and analysed by microcomputed tomography. A significant increase in bone formation was observed in Matrigel treated with µsp DBD compared with control, while a significant decrease in bone formation was observed for both nsp treatments. Histological and immunohistochemical analysis showed Matrigel treated with µsp plasma increased the number of invading cells, the amount of vascular endothelial growth factor and chondrogenesis while the opposite was true for Matrigel treated with nsp plasma. In support of the in vivo Matrigel study, 10 T1/2 cells cultured in vitro on µsp DBD-treated type I collagen showed increased expression of adhesion proteins and activation of survival pathways, which decreased with nsp plasma treatments. These results indicate DBD modification of ECM can influence cellular behaviours to accelerate or inhibit chondrogenesis and endochondral ossification.
机译:这项研究的目的是调查介电屏障放电(DBD)产生的冷等离子体是否会修饰细胞外基质(ECM)以影响软骨形成和软骨内骨化。软骨内骨化过程中用骨替代软骨对胎儿骨骼发育,骨骼生长和骨折愈合至关重要。 ECM对这一过程的调节是通过基质重塑进行的,涉及多种细胞附着分子和生长因子,这些因子会影响细胞的形态和蛋白质表达。将市售的ECM Matrigel用微秒或纳秒脉冲(分别为µsp或nsp)DBD频率条件以等效频率(1 kHz)或功率(〜1 W)进行处理。添加重组人骨形态发生蛋白2,并将该混合物皮下注射到小鼠中以模拟异位软骨内骨化。两周后,提取肿块并通过微计算机断层摄影术进行分析。与对照组相比,用µsp DBD处理的Matrigel的骨形成明显增加,而两种nsp处理的骨形成均显着减少。组织学和免疫组织化学分析显示,用µsp血浆处理的Matrigel增加了侵袭细胞的数量,血管内皮生长因子的数量和软骨形成,而用nsp血浆处理的Matrigel则相反。为了支持体内Matrigel研究,在µsp DBD处理的I型胶原上体外培养的10个T1 / 2细胞显示出粘附蛋白的表达增加和存活途径的激活,而nsp血浆处理则降低了。这些结果表明ECD的DBD修饰可以影响细胞行为,以加速或抑制软骨形成和软骨内骨化。

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