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Synergistic effects on mesenchymal stem cell-based cartilage regeneration by chondrogenic preconditioning and mechanical stimulation

机译:软骨预处理和机械刺激对基于间充质干细胞的软骨再生的协同作用

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Background Mesenchymal stem cells (MSCs) hold promising translational potential in cartilage regeneration. However, the efficacy of MSC-based tissue engineering is not satisfactory in the treatment of cartilage defect because of the inevitable cellular functional changes during ex vivo cell expansion. How to maintain the chondrogenic capacity of MSCs to improve their therapeutic outcomes remains an outstanding question. Methods Bone marrow-derived MSCs were firstly primed in chondrogenic induction medium which was then replaced with normal growth medium to attain the manipulated cells (M-MSCs). Methacrylated hyaluronic acid (MeHA) was synthesized as a scaffold to encapsulate the cells. The MSC- or M-MSC-laden constructs were treated with dynamic compressive loading (DL) in a bioreactor or with free loading (FL) for 14?days. Afterwards, the constructs were implanted in nude mice or rat models of osteochondral defects to test their efficiency in cartilage regeneration or repair. Results Data showed that the resulting M-MSCs exhibited superior chondrogenic differentiation potential and survivability compared with untreated MSCs. More importantly, we found that DL significantly promoted neocartilage formation in the MeHA hydrogel encapsulated with M-MSCs after 30?days of implantation in nude mice. Furthermore, the constructs laden with M-MSCs after DL for 14?days significantly enhanced cartilage healing in a rat model of osteochondral defect. Conclusions Findings from this study highlight the importance of maintaining chondrogenic potential of MSCs by in-vitro chondrogenic preconditioning and a synergistic effect of mechanical stimulation in cartilage engineering, which may shed light on the stem cell-based tissue engineering for cartilage repair.
机译:背景间充质干细胞(MSCs)在软骨再生中具有有希望的翻译潜力。然而,基于MSC的组织工程的功效在软骨缺损的治疗中并不令人满意,因为在离体细胞扩增期间不可避免的细胞功能改变。如何维持MSC的软骨形成能力以改善其治疗结果仍然是一个悬而未决的问题。方法首先将骨髓源性间充质干细胞在软骨诱导培养基中灌注,然后用正常生长培养基代替以获取被操纵细胞(M-MSCs)。合成甲基丙烯酸化的透明质酸(MeHA)作为支架来封装细胞。载有MSC或M-MSC的构建体在生物反应器中用动态压缩负载(DL)或在自由负载(FL)中处理14天。之后,将所述构建体植入裸鼠或骨软骨缺损的大鼠模型中,以测试其在软骨再生或修复中的效率。结果数据表明,与未处理的MSC相比,所得的M-MSC显示出优异的软骨分化潜能和存活性。更重要的是,我们发现在裸鼠植入30天后,DL显着促进了用M-MSC包裹的MeHA水凝胶中新软骨的形成。此外,在DL术后14天携带M-MSC的构建体在骨软骨缺损的大鼠模型中显着增强了软骨的愈合。结论这项研究的发现突出了通过体外软骨形成预处理保持MSCs软骨形成潜力的重要性以及机械刺激在软骨工程中的协同作用,这可能为基于干细胞的组织工程修复软骨提供了启示。

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