Photo-driven dynamic hydrogel modulates bone marrow mesenchymal stem cells behavior for enhanced cartilage regeneration

被引:3
作者
Zhang, Wenjie [1 ,2 ]
Xue, Wenliang [1 ,3 ]
Jia, Zhaoli [4 ]
Yang, Rong [1 ,2 ]
Wang, Penghui [1 ,2 ]
Hu, Yi [5 ]
Tan, Xiaoyan [1 ,3 ]
Chen, Qiang [4 ,6 ]
Chi, Bo [1 ,3 ]
机构
[1] Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
[2] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Peoples R China
[3] Nanjing Tech Univ, Coll Food Sci & Light Ind, Nanjing 211816, Peoples R China
[4] Nanjing Univ, High Tech Res Inst, Changzhou 213164, Peoples R China
[5] Nanjing Tech Univ, Sch Pharmaceut Sci, Nanjing 211816, Peoples R China
[6] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210093, Peoples R China
关键词
Living hydrogel; Cartilage repair; Dynamic matrix; Viscoelasticity; BMSCs; MATRIX; DIFFERENTIATION; PROLIFERATION; COLLAGEN;
D O I
10.1016/j.cej.2024.149689
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Regenerating damaged cartilage remains a challenge due to limited cell availability and inefficient chondrogenic differentiation. Here, we present a photo-driven dynamic hydrogel with a double-network structure to meet this challenge. The fabrication strategy involves a combination of a photosensitive host-guest network with a covalent network, providing tunable mechanical cues that effectively regulate bone marrow mesenchymal stem cells (BMSCs) behavior within their microenvironment while maintaining macroscopical stability. Employing a two-step stiffness-tunable process mediated by controlled low-dose light exposure, the hydrogel exerts precise control over BMSCs proliferation and orchestrates chondrogenic differentiation, leading to the upregulation of crucial chondrogenic genes, notably SOX9 and ACAN. Empirical evidence derived from histological analysis substantiates the functional efficacy of the hydrogel, confirming the regenerative potential of cartilage tissues. This study presents an innovative and promising strategy for stem cell culture, in vitro differentiation, and cell delivery, with implications for cartilage defect repair and tissue regeneration.
引用
收藏
页数:14
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