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TGF-β3 固定化 PLGA-明胶/硫酸软骨素/透明质酸杂化支架用于软骨再生。

TGF-β3 immobilized PLGA-gelatin/chondroitin sulfate/hyaluronic acid hybrid scaffold for cartilage regeneration.

机构信息

Department of Orthopaedic Surgery, Xi-jing Hospital, the Fourth Military Medical University, Xi'an, China.

出版信息

J Biomed Mater Res A. 2010 Dec 15;95(4):982-92. doi: 10.1002/jbm.a.32899. Epub 2010 Sep 24.

Abstract

Although most in vitro studies indicate that transforming growth factor β3 (TGF-β3) immobilized scaffold is suitable for cartilage tissue engineering, in vivo studies of implanting immobilized scaffold for chondral defect repair are still lacking. This study is to evaluate the potentials of TGF-β3 immobilized poly-(lactic-co-glycolic acid)-gelatin/chondroitin sulfate/hyaluronic acid (PLGA-GCH) hybrid scaffold for cartilage regeneration. The scaffold was fabricated by incorporating GCH micro-sponges into PLGA frameworks and then crosslinked with TGF-β3 to mimic natural cartilaginous extra cellular matrix (ECM). In vitro study demonstrated that MSCs proliferated vigorously and produced abundant ECM on scaffold. The immunohistochemistry staining and alcian blue staining confirmed the cartilaginous ECM production. The chondrogenic differentiation of MSCs on scaffold was proved by the expression of collagen II gene in mRNA and protein level. Then MSCs/TGF-β3 immobilized scaffolds were implanted in rabbits for chondral defects repair. After eight weeks, histological observation showed that differentiated MSCs were located in lacunae within the metachromatic staining matrix and exhibited typical chondrocyte morphology. Histological grading scores also indicated the congruent cartilage was regenerated. In conclusion, the TGF-β3 immobilized PLGA-GCH hybrid scaffold has great potential in constructing the tissue-engineered cartilage.

摘要

虽然大多数体外研究表明,转化生长因子 β3(TGF-β3)固定化支架适合软骨组织工程,但植入固定化支架修复软骨缺损的体内研究仍然缺乏。本研究旨在评估 TGF-β3 固定化聚(乳酸-共-乙醇酸)-明胶/硫酸软骨素/透明质酸(PLGA-GCH)杂化支架在软骨再生中的潜力。该支架通过将 GCH 微球掺入 PLGA 支架中,并与 TGF-β3 交联来模拟天然软骨细胞外基质(ECM)。体外研究表明,MSCs 在支架上大量增殖并产生丰富的 ECM。免疫组织化学染色和阿利新蓝染色证实了软骨 ECM 的产生。MSCs 在支架上的软骨分化通过 mRNA 和蛋白水平的胶原 II 基因表达得到证实。然后将 MSCs/TGF-β3 固定化支架植入兔软骨缺损处进行修复。8 周后,组织学观察显示,分化的 MSCs 位于染色基质的陷窝内,呈现典型的软骨细胞形态。组织学分级评分也表明了一致的软骨再生。总之,TGF-β3 固定化 PLGA-GCH 杂化支架在构建组织工程软骨方面具有很大的潜力。

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