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非甾体抗炎药对马间充质干细胞增殖、分化和迁移的影响。

Effects of non-steroidal anti-inflammatory drugs on proliferation, differentiation and migration in equine mesenchymal stem cells.

机构信息

Department of Anatomy I, University of Cologne, Cologne, Germany.

出版信息

Cell Biol Int. 2011 Mar;35(3):235-48. doi: 10.1042/CBI20090211.

Abstract

In equine medicine, stem cell therapies for orthopaedic diseases are routinely accompanied by application of NSAIDs (non-steroidal anti-inflammatory drugs). Thus, it has to be analysed how NSAIDs actually affect the growth and differentiation potential of MSCs (mesenchymal stem cells) in vitro in order to predict the influence of NSAIDs such as phenylbutazone, meloxicam, celecoxib and flunixin on MSCs after grafting in vivo. The effects of NSAIDs were evaluated regarding cell viability and proliferation. Additionally, the multilineage differentiation capacity and cell migration was analysed. NSAIDs at lower concentrations (0.1-1 μM for celecoxib and meloxicam and 10-50 μM for flunixin) exert a positive effect on cell proliferation and migration, while at higher concentrations (10-200 μM for celecoxib and meloxicam and 100-1000 μM for flunixin and phenylbutazone), there is rather a negative influence. While there is hardly any influence on the adipogenic as well as on the chondrogenic MSC differentiation, the osteogenic differentiation potential, as demonstrated with the von Kossa staining, is significantly disturbed. Thus, it can be concluded that the effects of NSAIDs on MSCs are largely dependent on the concentrations used. Additionally, for some differentiation lineages, also the choice of NSAID is critical.

摘要

在马医学中,干细胞疗法常用于治疗骨科疾病,同时还会配合使用 NSAIDs(非甾体抗炎药)。因此,我们必须分析 NSAIDs 实际上如何在体外影响间充质干细胞(MSCs)的生长和分化潜能,以便预测体内移植后 NSAIDs(如苯丁唑酮、美洛昔康、塞来昔布和氟尼辛)对 MSCs 的影响。我们评估了 NSAIDs 对细胞活力和增殖的影响。此外,还分析了多谱系分化能力和细胞迁移。较低浓度的 NSAIDs(塞来昔布和美洛昔康为 0.1-1 μM,氟尼辛为 10-50 μM)对细胞增殖和迁移有积极影响,而较高浓度的 NSAIDs(塞来昔布和美洛昔康为 10-200 μM,氟尼辛和苯丁唑酮为 100-1000 μM)则有负面影响。虽然对脂肪形成和软骨形成 MSC 分化几乎没有影响,但 von Kossa 染色显示,成骨分化潜能受到显著干扰。因此,可以得出结论,NSAIDs 对 MSCs 的影响在很大程度上取决于使用的浓度。此外,对于某些分化谱系,NSAID 的选择也很关键。

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