| Literature DB >> 33363129 |
Yanhong Zhao1,2, Xige Zhao1,2, Rui Zhang1,2, Ying Huang1,2, Yunjie Li1,2, Minhui Shan1,2, Xintong Zhong1,2, Yi Xing1,2, Min Wang1,2, Yang Zhang3, Yanmei Zhao4.
Abstract
Repair of articular cartilage defects is a challenging aspect of clinical treatment. Kartogenin (KGN), a small molecular compound, can induce the differentiation of bone marrow-derived mesenchymal stem cells (BMSCs) into chondrocytes. Here, we constructed a scaffold based on chondrocyte extracellular matrix (CECM) and poly(lactic-co-glycolic acid) (PLGA) microspheres (MP), which can slowly release KGN, thus enhancing its efficiency. Cell adhesion, live/dead staining, and CCK-8 results indicated that the PLGA(KGN)/CECM scaffold exhibited good biocompatibility. Histological staining and quantitative analysis demonstrated the ability of the PLGA(KGN)/CECM composite scaffold to promote the differentiation of BMSCs. Macroscopic observations, histological tests, and specific marker analysis showed that the regenerated tissues possessed characteristics similar to those of normal hyaline cartilage in a rabbit model. Use of the PLGA(KGN)/CECM scaffold may mimic the regenerative microenvironment, thereby promoting chondrogenic differentiation of BMSCs in vitro and in vivo. Therefore, this innovative composite scaffold may represent a promising approach for acellular cartilage tissue engineering.Entities:
Keywords: cartilage tissue engineering; composite scaffold; decellularized cartilage extracellular matrix; kartogenin; poly(lactic-co-glycolic acid)
Year: 2020 PMID: 33363129 PMCID: PMC7756004 DOI: 10.3389/fbioe.2020.600103
Source DB: PubMed Journal: Front Bioeng Biotechnol ISSN: 2296-4185