Accelerated cartilage regeneration through immunomodulation and enhanced chondrogenesis by an extracellular matrix hydrogel encapsulating Kartogenin

被引:2
|
作者
Huang, Kai [1 ,2 ]
Zhang, Qing-Yi [1 ,2 ]
Tan, Jie [1 ,2 ]
Nie, Rong [1 ,2 ]
Feng, Zi-Yuan [1 ,2 ]
Liu, Yuan [1 ,2 ]
Sheng, Ning [1 ,2 ]
Li, He-Xi [1 ,2 ]
Zhang, Yue-Qi [1 ,2 ]
Shen, Bin [1 ,2 ]
Xie, Hui-Qi [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, Stem Cell & Tissue Engn Res Ctr, Dept Orthoped Surg,State Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, Orthoped Res Inst, Chengdu 610041, Sichuan, Peoples R China
[3] Frontier Med Ctr, Tianfu Jincheng Lab, Chengdu 610212, Sichuan, Peoples R China
关键词
Small intestinal submucosa; Kartogenin; Immunomodulation; Cartilage defect; INFLAMMATION; DIFFERENTIATION; INJURY;
D O I
10.1016/j.cej.2024.154993
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Articular cartilage is crucial for the functional integrity of joints yet vulnerable to a spectrum of injuries. The adverse immune microenvironment ensuing from injury, coupled with the intrinsic property of the tissue characterized by limited cellularity, poses a significant challenge to the reconstruction of cartilage defect. In this study, an extracellular matrix hydrogel derived from porcine small intestinal submucosa (SIS) with encapsulation of Kartogenin (KGN) has been designed for the cartilage repair and regeneration. The SIS hydrogel, which possessed a three-dimensional porous structure akin to the natural cartilage, has provided a scaffold essential for the progenitor cells engaged in the repair process and sustained release of KGN. As shown by in vitro experiments, the KGN could recruit host endogenous bone marrow-derived mesenchymal stem cells (BMSCs) and induce them to differentiate into chondrocytes, thus enabling in situ cartilage regeneration without cell transplantation. Notably, the bioactive component of SIS was further revealed to possess excellent immunomodulatory capacity to induce the phenotypic shift from M1 to M2 macrophages, which could enhance the chondrogenic differentiation of BMSCs indirectly. Additionally, in vivo experiments showed that the regenerated tissues of the composite SIS hydrogel group were close to the natural hyaline cartilage. Leveraging the combined effects of KGN and SIS hydrogel, this innovative composite material shows great potential as a biomaterial for effective cartilage repair and regeneration.
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页数:15
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