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萘普生对人骨髓间充质干细胞软骨形成的影响。

The Effects of Naproxen on Chondrogenesis of Human Mesenchymal Stem Cells.

作者信息

Antoniou John, Wang Hong Tian, Hadjab Insaf, Aldebeyan Sultan, Alaqeel Motaz A, Meij Björn P, Tryfonidou Marianna A, Mwale Fackson

机构信息

1 Lady Davis Institute for Medical Research, Jewish General Hospital, McGill University , Montreal, Quebec, Canada .

2 Division of Orthopedic Surgery, McGill University , Montreal, Quebec, Canada .

出版信息

Tissue Eng Part A. 2015 Jul;21(13-14):2136-46. doi: 10.1089/ten.TEA.2014.0668. Epub 2015 May 18.

Abstract

Currently, there are no established treatments to prevent, stop, or even retard the degeneration of articular cartilage in osteoarthritis (OA). Biological repair of the degenerating articular cartilage would be preferable to surgery. There is no benign site where autologous chondrocytes can be harvested and used as a cell source for cartilage repair, leaving mesenchymal stem cells (MSCs) as an attractive option. However, MSCs from OA patients have been shown to constitutively express collagen type X (COL-X), a marker of late-stage chondrocyte hypertrophy. We recently found that naproxen (Npx), but not other nonsteroidal anti-inflammatory drugs, can induce collagen type X alpha 1 (COL10A1) gene expression in bone marrow-derived MSCs from healthy and OA donors. In this study, we determined the effect of Npx on COL10A1 expression and investigated the intracellular signaling pathways that mediate such effect in normal human MSCs during chondrogenesis. MSCs were cultured in standard chondrogenic differentiation media supplemented with or without Npx. Our results show that Npx can regulate chondrogenic differentiation by affecting the gene expression of both Indian hedgehog and parathyroid hormone/parathyroid hormone-related protein signaling pathways in a time-dependent manner, suggesting a complex interaction of different signaling pathways during the process.

摘要

目前,尚无成熟的治疗方法来预防、阻止甚至延缓骨关节炎(OA)中关节软骨的退变。对于退变的关节软骨,生物修复比手术更可取。没有可以采集自体软骨细胞并用作软骨修复细胞来源的良性部位,这使得间充质干细胞(MSCs)成为一个有吸引力的选择。然而,OA患者的MSCs已被证明组成性表达X型胶原(COL-X),这是晚期软骨细胞肥大的标志物。我们最近发现,萘普生(Npx),而非其他非甾体抗炎药,可诱导健康供体和OA供体的骨髓来源MSCs中X型胶原α1(COL10A1)基因表达。在本研究中,我们确定了Npx对COL10A1表达的影响,并研究了在软骨形成过程中正常人类MSCs中介导这种作用的细胞内信号通路。MSCs在添加或不添加Npx的标准软骨分化培养基中培养。我们的结果表明,Npx可通过以时间依赖性方式影响印度刺猬因子和甲状旁腺激素/甲状旁腺激素相关蛋白信号通路的基因表达来调节软骨分化,这表明在此过程中不同信号通路存在复杂的相互作用。

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