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采用两相静电纺丝法将负载生长因子的壳聚糖纳米颗粒掺入静电纺丝纤维支架中,以保留生物活性并促进软骨再生。

Two-phase electrospinning to incorporate growth factors loaded chitosan nanoparticles into electrospun fibrous scaffolds for bioactivity retention and cartilage regeneration.

作者信息

Wang Chongyang, Hou Wenxiu, Guo Xuran, Li Juehong, Hu Tu, Qiu Manle, Liu Shen, Mo Xiumei, Liu Xudong

机构信息

Department of Orthopaedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dongchuan RD, Shanghai, China.

出版信息

Mater Sci Eng C Mater Biol Appl. 2017 Oct 1;79:507-515. doi: 10.1016/j.msec.2017.05.075. Epub 2017 May 14.

DOI:10.1016/j.msec.2017.05.075
PMID:28629047
Abstract

Growth factor is an essential ingredient to regulate mesenchymal stem cells (MSCs) chondrogenic differentiation in cartilage tissue engineering. However, non-osteochondral specification, short plasma half time and bioactivity loss restrict growth factor's application. Thus, novel chondrogenic growth factors, specifically target osteochondral lineage cells, that can be sustained release and bioactivity protected to exert functions continually and effectively have attracted increasing researchers' interest. To achieve these goals, chitosan nanoparticles and electrospun fiber scaffolds were used as dual release system to sustain release Nel-like molecule-1 (Nell-1) growth factor and protect bioactivity, then the effect and mechanism of Nell-1 on inducing human bone MSCs (hBMSCs) differentiate toward chondrocytes were investigated. For release and bioactivity protection study, preloading Nell-1 into chitosan nanoparticles significantly extended the release time, increased the released Nell-1's bioactivity than directly incorporating Nell-1 into the scaffolds. Furthermore, Nell-1 specifically promotes hBMSCs in vitro chondrogenic differentiation by increasing expression of chondrogenic related genes and proteins. These findings suggest the potential utility of Nell-1 incorporated dual release scaffold for cartilage tissue engineering.

摘要

生长因子是调节软骨组织工程中骨髓间充质干细胞(MSCs)软骨分化的重要成分。然而,非骨软骨特异性、血浆半衰期短和生物活性丧失限制了生长因子的应用。因此,新型软骨生成生长因子,特别是靶向骨软骨谱系细胞,能够持续释放并保护生物活性以持续有效地发挥功能,已引起越来越多研究人员的兴趣。为实现这些目标,壳聚糖纳米颗粒和电纺纤维支架被用作双重释放系统,以持续释放尼尔样分子-1(Nell-1)生长因子并保护其生物活性,随后研究了Nell-1诱导人骨MSCs(hBMSCs)向软骨细胞分化的作用及机制。对于释放和生物活性保护研究,将Nell-1预载入壳聚糖纳米颗粒显著延长了释放时间,与直接将Nell-1掺入支架相比,增加了释放的Nell-1的生物活性。此外,Nell-1通过增加软骨生成相关基因和蛋白质的表达,特异性促进hBMSCs在体外的软骨分化。这些发现表明,掺入Nell-1的双重释放支架在软骨组织工程中具有潜在应用价值。

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