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SOX9 基因联合肝素化 TGF-β3 包被载有地塞米松的 PLGA 微球诱导人骨髓间充质干细胞软骨分化。

SOX9 gene plus heparinized TGF-β 3 coated dexamethasone loaded PLGA microspheres for inducement of chondrogenesis of hMSCs.

机构信息

Department of Biomedical Science, College of Life Science, CHA University, Bundang-gu, Seongnam-si, Republic of Korea.

出版信息

Biomaterials. 2012 Oct;33(29):7151-63. doi: 10.1016/j.biomaterials.2012.06.023. Epub 2012 Jul 11.

Abstract

Microparticulated types of scaffolds have been widely applied in stem cell therapy and the tissue engineering field for the regeneration of wound tissues. During application of simple genes or growth factors and cell delivery vehicles, we designed a method that employs dexamethsone loaded PLGA microspheres consisting of polyplexed SOX9 genes plus heparinized TGF-β 3 on the surface of polymeric microspheres prepared using a layer-by-layer (LbL) method. The fabrication of the polyplexed SOX9 genes plus heparinized TGF-β 3 and their subsequent coating onto dexamethsone loaded PLGA microspheres represents a method for functionalization of the polymeric matrix. The use of SOX9 gene plus heparinized TGF-β 3 coated dexamethsone loaded PLGA microspheres was evaluated to determine their potential as both gene carriers and cell delivery vehicle. By adhesion of hMSCs onto SOX9 gene plus heparinized TGF-β 3 coated dexamethsone loaded PLGA microspheres, the chondrogenesis-related specific genes of collagen type II were increased 30 times comparing to control. Also, the specific extracellular matrix of glycosaminoglycan (GAG) production of hMSCs adhered onto SOX9 gene plus heparinized TGF-β 3 coated dexamethasone loaded PLGA microspheres increased more 2.5 times than control group. Not only in vitro culture but in vivo results, the specific genes of COMP, aggrecan, collagen type II, and SOX9 showed much more gene expressions such as 20, 15, 10, 8 times.

摘要

微粒型支架已广泛应用于干细胞治疗和组织工程领域,用于创伤组织的再生。在应用简单基因或生长因子和细胞输送载体时,我们设计了一种方法,即在通过层层(LbL)方法制备的聚合物微球表面上负载有地塞米松的 PLGA 微球上,包载 SOX9 基因加肝素化 TGF-β3 的多聚体。多聚体 SOX9 基因加肝素化 TGF-β3 的制备及其随后包被到负载地塞米松的 PLGA 微球上代表了聚合物基质功能化的一种方法。评估了负载 SOX9 基因加肝素化 TGF-β3 的地塞米松 PLGA 微球的使用,以确定它们作为基因载体和细胞输送载体的潜力。通过 hMSCs 黏附到负载 SOX9 基因加肝素化 TGF-β3 的地塞米松 PLGA 微球上,与对照组相比,胶原 II 型的软骨形成相关特异性基因增加了 30 倍。此外,黏附到负载 SOX9 基因加肝素化 TGF-β3 的地塞米松 PLGA 微球上的 hMSCs 的细胞外基质糖胺聚糖(GAG)的特异性产生增加了 2.5 倍以上。不仅在体外培养中,而且在体内结果中,COMP、聚集蛋白聚糖、胶原 II 型和 SOX9 的特异性基因表达也增加了 20、15、10、8 倍。

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