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聚(L-谷氨酸)/壳聚糖支架中原位生成间充质干细胞多细胞球体用于透明样软骨再生。

In-situ birth of MSCs multicellular spheroids in poly(L-glutamic acid)/chitosan scaffold for hyaline-like cartilage regeneration.

机构信息

Department of Polymer Materials, Shanghai University, 99 Shangda Road, Shanghai 200444, PR China.

Medical Science & Research Center, Beijing Shijitan Hospital, Capital Medical University, 10 Tieyi Road, Beijing 100038, PR China.

出版信息

Biomaterials. 2015 Dec;71:24-34. doi: 10.1016/j.biomaterials.2015.08.037. Epub 2015 Aug 20.

Abstract

The success of mesenchymal stem cells (MSCs) based articular cartilage tissue engineering is limited by the presence of fibrous tissue in generated cartilage, which is associated with the current scaffold strategy that promotes cellular adhesion and spreading. Here we design a non-fouling scaffold based on amide bonded poly(l-glutamic acid) (PLGA) and chitosan (CS) to drive adipose stem cells (ASCs) to aggregate to form multicellular spheroids with diameter of 80-110 μm in-situ. To illustrate the advantage of the present scaffolds, a cellular adhesive scaffold based on the same amide bonded PLGA and CS was created through a combination of air-drying and freeze-drying to limit the hydration effect while also achieving porous structure. Compared to ASCs spreading along the surface of pores within scaffold, the dense mass of aggregated ASCs in PLGA/CS scaffold exhibited enhanced chondrogenic differentiation capacity, as determined by up-regulated GAGs and COL II expression, and greatly decreased COL I deposition during in vitro chondrogenesis. Furthermore, after 12 weeks of implantation, neo-cartilages generated by ASCs adhered on scaffold significantly presented fibrous matrix which was characterized by high levels of COL I deposition. However, neo-cartilage at 12 weeks post-implantation generated by PLGA/CS scaffold carrying ASC spheroids possessed similar high level of GAGs and COL II and low level of COL I as that in normal cartilage. The in vitro and in vivo results indicated the present strategy could not only promote chondrogenesis of ASCs, but also facilitate hyaline-like cartilage regeneration with reduced fibrous tissue formation which may attenuate cartilage degradation in future long-term follow-up.

摘要

基于间充质干细胞(MSCs)的关节软骨组织工程的成功受到生成软骨中纤维组织的限制,这与当前促进细胞黏附和铺展的支架策略有关。在这里,我们设计了一种基于酰胺键合聚(L-谷氨酸)(PLGA)和壳聚糖(CS)的非缠结支架,以驱动脂肪干细胞(ASCs)聚集形成直径为 80-110μm 的多细胞球体。为了说明本支架的优势,通过空气干燥和冷冻干燥相结合,创建了一种基于相同酰胺键合的 PLGA 和 CS 的细胞黏附支架,以限制水合作用的影响,同时实现多孔结构。与 ASCs 沿着支架内孔表面铺展相比,PLGA/CS 支架中密集的聚集 ASCs 表现出增强的软骨分化能力,这表现为 GAGs 和 COL II 的表达上调,以及在体外软骨形成过程中 COL I 的沉积大大减少。此外,植入 12 周后,附着在支架上的 ASCs 产生的新软骨明显呈现出富含 COL I 沉积的纤维基质。然而,PLGA/CS 支架携带 ASC 球体植入 12 周后产生的新软骨,其 GAGs 和 COL II 水平较高,COL I 水平较低,与正常软骨相似。体外和体内结果表明,该策略不仅可以促进 ASCs 的软骨分化,还可以促进透明软骨样再生,减少纤维组织形成,从而可能减轻未来长期随访中的软骨降解。

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