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软骨生成诱导过程中人间充质干细胞分泌组的差异。

Differences in human mesenchymal stem cell secretomes during chondrogenic induction.

作者信息

Gardner O F, Fahy N, Alini M, Stoddart M J

机构信息

AO Research Institute Davos, Clavadelerstrasse 8, 7270 Davos Platz,

出版信息

Eur Cell Mater. 2016 Apr 10;31:221-35. doi: 10.22203/ecm.v031a15.

Abstract

Mesenchymal stem cells (MSCs) can be induced towards chondrogenesis through the application of chondrogenic stimuli such as transforming growth factor-β (TGF-β) or by multiaxial mechanical load. Previous work has showed that the chondrogenic effect of multiaxial load on MSCs is mediated by the endogenous production of TGF-β1 by stimulated cells. This work compared the effects of TGF-β1 stimulation and multiaxial mechanical load on the secretomes of stimulated cells. MSCs were seeded into fibrin-poly(ester-urethane) scaffolds and chondrogenically stimulated with either TGF-β1 or mechanical load. The culture media was collected and analysed for 174 proteins using a cytokine antibody array. The results of the secretome analysis were then confirmed at a gene expression level by real-time PCR. As results implicated nitric oxide (NO), the media nitrite content was also determined as an indirect measurement of media NO levels. Results showed that TGF-β1 stimulation and mechanical load lead to similar changes in factors such as BLC, VEGF and MMP13, whilst differences in detected levels were seen for factors including leptin, MDC, MIP3α and LAP. Gene expression analysis confirmed significant changes in four factors: angiopoietin 2, GROα, MMP13 and osteoprotegerin. After one week in culture the media nitrite content was significantly higher in loaded groups than both control and TGF-β1 stimulated groups, suggesting this may be a major therapeutic target. These data show that despite clear similarities, TGF-β1 stimulation and load have distinct effects on MSCs and are not analogous. This study has identified a number of potentially novel targets for tissue engineering, these data may also be useful for improving rehabilitation protocols e.g. after microfracture.

摘要

间充质干细胞(MSCs)可通过应用软骨生成刺激因子(如转化生长因子-β(TGF-β))或多轴机械负荷诱导其向软骨生成方向分化。先前的研究表明,多轴负荷对MSCs的软骨生成作用是由受刺激细胞内源性产生的TGF-β1介导的。本研究比较了TGF-β1刺激和多轴机械负荷对受刺激细胞分泌组的影响。将MSCs接种到纤维蛋白-聚(酯-聚氨酯)支架中,并用TGF-β1或机械负荷进行软骨生成刺激。收集培养基,使用细胞因子抗体阵列分析174种蛋白质。然后通过实时PCR在基因表达水平上确认分泌组分析的结果。由于结果涉及一氧化氮(NO),还测定了培养基中亚硝酸盐含量作为培养基NO水平的间接测量指标。结果表明,TGF-β1刺激和机械负荷导致诸如BLC、VEGF和MMP13等因子发生类似变化,而瘦素、MDC、MIP3α和LAP等因子的检测水平存在差异。基因表达分析证实了四种因子有显著变化:血管生成素2、GROα、MMP13和骨保护素。培养一周后,负荷组培养基中亚硝酸盐含量显著高于对照组和TGF-β1刺激组,表明这可能是一个主要的治疗靶点。这些数据表明,尽管TGF-β1刺激和负荷有明显的相似之处,但它们对MSCs有不同的影响,并非类似。本研究确定了一些组织工程潜在的新靶点,这些数据也可能有助于改进康复方案,例如微骨折后的康复方案。

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