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包埋于藻酸盐水凝胶共递送微囊化系统中的牙髓间充质干细胞用于软骨再生。

Dental mesenchymal stem cells encapsulated in an alginate hydrogel co-delivery microencapsulation system for cartilage regeneration.

机构信息

Center for Craniofacial Molecular Biology, Ostrow School of Dentistry, University of Southern California, Los Angeles, CA 90033, USA.

出版信息

Acta Biomater. 2013 Dec;9(12):9343-50. doi: 10.1016/j.actbio.2013.07.023. Epub 2013 Jul 26.

Abstract

Dental-derived mesenchymal stem cells (MSCs) are promising candidates for cartilage regeneration, with a high capacity for chondrogenic differentiation. This property helps make dental MSCs an advantageous therapeutic option compared to current treatment modalities. The MSC delivery vehicle is the principal determinant for the success of MSC-mediated cartilage regeneration therapies. The objectives of this study were to: (1) develop a novel co-delivery system based on TGF-β1 loaded RGD-coupled alginate microspheres encapsulating periodontal ligament stem cells (PDLSCs) or gingival mesenchymal stem cells (GMSCs); and (2) investigate dental MSC viability and chondrogenic differentiation in alginate microspheres. The results revealed the sustained release of TGF-β1 from the alginate microspheres. After 4 weeks of chondrogenic differentiation in vitro, PDLSCs and GMSCs as well as human bone marrow mesenchymal stem cells (hBMMSCs) (as positive control) revealed chondrogenic gene expression markers (Col II and Sox-9) via qPCR, as well as matrix positively stained by Toluidine Blue and Safranin-O. In animal studies, ectopic cartilage tissue regeneration was observed inside and around the transplanted microspheres, confirmed by histochemical and immunofluorescent staining. Interestingly, PDLSCs showed more chondrogenesis than GMSCs and hBMMSCs (p<0.05). Taken together, these results suggest that RGD-modified alginate microencapsulating dental MSCs make a promising candidate for cartilage regeneration. Our results highlight the vital role played by the microenvironment, as well as value of presenting inductive signals for viability and differentiation of MSCs.

摘要

牙源性间充质干细胞(MSCs)在软骨再生方面具有很大的潜力,具有很强的软骨分化能力。与当前的治疗方法相比,这一特性使牙源性 MSCs 成为一种有利的治疗选择。MSC 输送载体是 MSC 介导的软骨再生治疗成功的主要决定因素。本研究的目的是:(1)开发一种基于负载 TGF-β1 的 RGD 偶联藻酸钠微球包埋牙周膜干细胞(PDLSCs)或牙龈间充质干细胞(GMSCs)的新型共输送系统;(2)研究藻酸钠微球中牙源性 MSC 的活力和软骨分化。结果表明,TGF-β1 可从藻酸钠微球中持续释放。体外软骨分化 4 周后,PDLSCs、GMSCs 以及人骨髓间充质干细胞(hBMMSCs)(作为阳性对照)通过 qPCR 显示出软骨基因表达标志物(Col II 和 Sox-9),同时甲苯胺蓝和番红 O 也对基质进行了阳性染色。在动物研究中,在移植的微球内部和周围观察到异位软骨组织再生,通过组织化学和免疫荧光染色得到证实。有趣的是,PDLSCs 比 GMSCs 和 hBMMSCs 表现出更强的软骨形成能力(p<0.05)。综上所述,这些结果表明,RGD 修饰的藻酸钠微囊化牙源性 MSC 是软骨再生的一种很有前途的候选物。我们的结果强调了微环境的重要作用,以及为 MSC 的活力和分化提供诱导信号的价值。

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