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藻酸盐/透明质酸水凝胶递送系统的特性调节牙周膜干细胞向软骨谱系的分化。

Alginate/hyaluronic acid hydrogel delivery system characteristics regulate the differentiation of periodontal ligament stem cells toward chondrogenic lineage.

机构信息

Weintraub Center for Reconstructive Biotechnology, Division of Advanced Prosthodontics, School of Dentistry, University of California, Los Angeles, CA, USA.

Departamento de Odontologia Restauradora, Faculdade de Odontologia da UFMG, Belo Horizonte, Brazil.

出版信息

J Mater Sci Mater Med. 2017 Sep 15;28(10):162. doi: 10.1007/s10856-017-5974-8.

Abstract

Cartilage tissue regeneration often presents a challenging clinical situation. Recently, it has been shown that Periodontal Ligament Stem Cells (PDLSCs) possess high chondrogenic differentiation capacity. In this study, we developed a stem cell delivery system based on alginate/hyaluronic acid (HA) loaded with TGF-β1 ligand, encapsulating PDLSCs; and investigated the chondrogenic differentiation of encapsulated cells in alginate/HA hydrogel microspheres in vitro and in vivo. The results showed that PDLSCs, as well as human bone marrow mesenchymal stem cells (hBMMSCs), as the positive control, were stained positive for both toluidine blue and alcian blue staining, while exhibiting high levels of gene expression related to chondrogenesis (Col II, Aggrecan and Sox-9), as assessed via qPCR. The quantitative PCR analyses exhibited that the chondrogenic differentiation of encapsulated MSCs can be regulated by the modulus of elasticity of hydrogel delivery system, confirming the vital role of the microenvironment, and the presence of inductive signals for viability and differentiation of MSCs. In vivo, histological and immunofluorescence staining for chondrogenic specific protein markers confirmed ectopic cartilage-like tissue regeneration inside transplanted hydrogels. PDLSCs presented significantly greater capability for chondrogenic differentiation than hBMMSCs (P < 0.05). Altogether, our findings confirmed that alginate/HA hydrogels encapsulating PDLSCs are a promising candidate for cartilage regeneration.

摘要

软骨组织再生常常呈现出具有挑战性的临床情况。最近已经表明,牙周韧带干细胞(PDLSCs)具有高的软骨分化能力。在本研究中,我们开发了一种基于藻酸盐/透明质酸(HA)负载 TGF-β1 配体的干细胞递送系统,封装 PDLSCs;并研究了封装细胞在藻酸盐/HA 水凝胶微球中的体外和体内软骨分化。结果表明,PDLSCs 以及人骨髓间充质干细胞(hBMMSCs)作为阳性对照,甲苯胺蓝和阿利新蓝染色均呈阳性,并且通过 qPCR 评估显示与软骨形成相关的基因表达水平较高(Col II、Aggrecan 和 Sox-9)。定量 PCR 分析表明,水凝胶递送系统的弹性模量可调节封装 MSC 的软骨分化,证实了微环境的重要作用以及诱导 MSC 存活和分化的信号的存在。在体内,软骨特异性蛋白标志物的组织学和免疫荧光染色证实了移植水凝胶内异位软骨样组织再生。PDLSCs 比 hBMMSCs 表现出更强的软骨分化能力(P<0.05)。总之,我们的研究结果证实,封装 PDLSCs 的藻酸盐/HA 水凝胶是软骨再生的有前途的候选物。

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