Sodium hyaluronate supplemented culture medium combined with joint-simulating mechanical loading improves chondrogenic differentiation of human mesenchymal stem cells.

IF 3.2 3区 医学 Q3 CELL & TISSUE ENGINEERING European cells & materials Pub Date : 2021-06-06 DOI:10.22203/eCM.v041a40
G Monaco, A J El Haj, M Alini, M J Stoddart
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引用次数: 4

Abstract

In vitro models aim to recapitulate the in vivo situation. To more closely mimic the knee joint environment, current in vitro models need improvements to reflect the complexity of the native tissue. High molecular weight hyaluronan (hMwt HA) is one of the most abundant bioactive macromolecules in healthy synovial fluid, while shear and dynamic compression are two joint-relevant mechanical forces. The present study aimed at investigating the concomitant effect of joint-simulating mechanical loading (JSML) and hMwt HA-supplemented culture medium on the chondrogenic differentiation of primary human bone-marrow-derived mesenchymal stem cells (hBM-MSCs). hBM-MSC chondrogenesis was investigated over 28 d at the gene expression level and total DNA, sulphated glycosaminoglycan, TGF-β1 production and safranin O staining were evaluated. The concomitant effect of hMwt HA culture medium and JSML significantly increased cartilage-like matrix deposition and sulphated glycosaminoglycan synthesis, especially during early chondrogenesis. A stabilisation of the hBM-MSC-derived chondrocyte phenotype was observed through the reduced upregulation of the hypertrophic marker collagen X and an increase in the chondrogenic collagen type II/X ratio. A combination of JSML and hMwt HA medium better reflects the complexity of the in vivo synovial joint environment. Thus, JSML and hMwt HA medium will be two important features for joint-related culture models to more accurately predict the in vivo outcome, therefore reducing the need for animal studies. Reducing in vitro artefacts would enable a more reliable prescreening of potential cartilage repair therapies.

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透明质酸钠补充培养基联合关节模拟机械负荷促进人间充质干细胞成软骨分化。
体外模型旨在概括体内情况。为了更接近地模拟膝关节环境,目前的体外模型需要改进以反映天然组织的复杂性。高分子量透明质酸(hMwt HA)是健康滑液中最丰富的生物活性大分子之一,而剪切和动态压缩是两种与关节相关的机械力。本研究旨在探讨关节模拟机械负荷(JSML)和hMwt ha补充培养基对原代人骨髓间充质干细胞(hBM-MSCs)成软骨分化的共同影响。在基因表达水平上观察hBM-MSC软骨形成28 d,并评估总DNA、硫酸糖胺聚糖、TGF-β1的产生和红花素O染色。hMwt HA培养基和JSML的共同作用显著增加了软骨样基质沉积和硫酸糖胺聚糖合成,尤其是在软骨形成早期。通过减少增生性标志物胶原X的上调和软骨源性胶原II/X比例的增加,观察到hbm - msc衍生的软骨细胞表型的稳定。JSML和hMwt HA介质联合使用能更好地反映体内滑膜关节环境的复杂性。因此,JSML和hMwt HA培养基将成为关节相关培养模型的两个重要特征,以更准确地预测体内结果,从而减少对动物研究的需求。减少体外人工产物将使潜在软骨修复疗法的预筛选更加可靠。
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来源期刊
European cells & materials
European cells & materials 生物-材料科学:生物材料
CiteScore
6.00
自引率
6.50%
发文量
55
审稿时长
1.5 months
期刊介绍: eCM provides an interdisciplinary forum for publication of preclinical research in the musculoskeletal field (Trauma, Maxillofacial (including dental), Spine and Orthopaedics). The clinical relevance of the work must be briefly mentioned within the abstract, and in more detail in the paper. Poor abstracts which do not concisely cover the paper contents will not be sent for review. Incremental steps in research will not be entertained by eCM journal.Cross-disciplinary papers that go across our scope areas are welcomed.
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