Zhi He , Peilun Hu , Zifan Li , Kaige Mao , Jingchuan Zheng , Chun-Yi Yang , Yuyang Luo , Jia Yang , Zheng Cao , Jingsong Lu , Xiaobin Luo , Sengpav Tong , Zhijun He , Kunkoo Kim , Yaosai Liu , Xiaodan Sun , Lingyun Zhao , Yongwei Pan , Yongping Cao , Yu Wang , Xiumei Wang
{"title":"自组装的混合水凝胶微球为骨骼再生创造了一个模拟骨髓的生态位","authors":"Zhi He , Peilun Hu , Zifan Li , Kaige Mao , Jingchuan Zheng , Chun-Yi Yang , Yuyang Luo , Jia Yang , Zheng Cao , Jingsong Lu , Xiaobin Luo , Sengpav Tong , Zhijun He , Kunkoo Kim , Yaosai Liu , Xiaodan Sun , Lingyun Zhao , Yongwei Pan , Yongping Cao , Yu Wang , Xiumei Wang","doi":"10.1016/j.bioactmat.2025.08.003","DOIUrl":null,"url":null,"abstract":"<div><div>Bone marrow (BM), a natural niche rich in growth factors and bone marrow mesenchymal stem cells (BMSCs), provides an optimal regenerative microenvironment and is widely used in clinical applications. However, the limited proliferative capacity of BMSCs and the mismatch between bone regeneration and growth factors release constrain their effectiveness in treating critical bone defects. Drawing inspiration from the regenerative properties of BM, we developed self-assembled hybrid microspheres to replicate its function and address these challenges through a tissue engineering approach. This BM-mimicking niche enriched BMSCs via fast-degrading gelatin methacryloyl (GelMA) microspheres, which were loaded with exogenous BMSCs and conjugated with stem cell homing peptides (SKP) to recruit endogenous BMSCs. SKP further enhanced the stemness of BMSCs, thereby promoting angiogenesis and resolving inflammation. Slow-degrading chitosan methacryloyl (ChitoMA) microspheres facilitated sustained release of angiogenic (KLT) and osteogenic (OGP) peptides, supporting blood vessel maturation and osteogenesis. The early release of BMSCs and SKP, followed by the subsequent release of OGP and KLT, aligned with the dynamic process of bone regeneration. In a rat critical femoral condyle defect model, the BM-mimicking niche formed an in-situ ossification center, significantly enhancing bone regeneration. This study introduces a novel BM-mimicking niche characterized by a BMSC-enriched environment and the sequential release of therapeutic factors, offering a promising strategy for treating critical bone defects.</div></div>","PeriodicalId":8762,"journal":{"name":"Bioactive Materials","volume":"54 ","pages":"Pages 179-200"},"PeriodicalIF":18.0000,"publicationDate":"2025-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-assembled hybrid hydrogel microspheres create a bone marrow-mimicking niche for bone regeneration\",\"authors\":\"Zhi He , Peilun Hu , Zifan Li , Kaige Mao , Jingchuan Zheng , Chun-Yi Yang , Yuyang Luo , Jia Yang , Zheng Cao , Jingsong Lu , Xiaobin Luo , Sengpav Tong , Zhijun He , Kunkoo Kim , Yaosai Liu , Xiaodan Sun , Lingyun Zhao , Yongwei Pan , Yongping Cao , Yu Wang , Xiumei Wang\",\"doi\":\"10.1016/j.bioactmat.2025.08.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Bone marrow (BM), a natural niche rich in growth factors and bone marrow mesenchymal stem cells (BMSCs), provides an optimal regenerative microenvironment and is widely used in clinical applications. However, the limited proliferative capacity of BMSCs and the mismatch between bone regeneration and growth factors release constrain their effectiveness in treating critical bone defects. Drawing inspiration from the regenerative properties of BM, we developed self-assembled hybrid microspheres to replicate its function and address these challenges through a tissue engineering approach. This BM-mimicking niche enriched BMSCs via fast-degrading gelatin methacryloyl (GelMA) microspheres, which were loaded with exogenous BMSCs and conjugated with stem cell homing peptides (SKP) to recruit endogenous BMSCs. SKP further enhanced the stemness of BMSCs, thereby promoting angiogenesis and resolving inflammation. Slow-degrading chitosan methacryloyl (ChitoMA) microspheres facilitated sustained release of angiogenic (KLT) and osteogenic (OGP) peptides, supporting blood vessel maturation and osteogenesis. The early release of BMSCs and SKP, followed by the subsequent release of OGP and KLT, aligned with the dynamic process of bone regeneration. In a rat critical femoral condyle defect model, the BM-mimicking niche formed an in-situ ossification center, significantly enhancing bone regeneration. 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Self-assembled hybrid hydrogel microspheres create a bone marrow-mimicking niche for bone regeneration
Bone marrow (BM), a natural niche rich in growth factors and bone marrow mesenchymal stem cells (BMSCs), provides an optimal regenerative microenvironment and is widely used in clinical applications. However, the limited proliferative capacity of BMSCs and the mismatch between bone regeneration and growth factors release constrain their effectiveness in treating critical bone defects. Drawing inspiration from the regenerative properties of BM, we developed self-assembled hybrid microspheres to replicate its function and address these challenges through a tissue engineering approach. This BM-mimicking niche enriched BMSCs via fast-degrading gelatin methacryloyl (GelMA) microspheres, which were loaded with exogenous BMSCs and conjugated with stem cell homing peptides (SKP) to recruit endogenous BMSCs. SKP further enhanced the stemness of BMSCs, thereby promoting angiogenesis and resolving inflammation. Slow-degrading chitosan methacryloyl (ChitoMA) microspheres facilitated sustained release of angiogenic (KLT) and osteogenic (OGP) peptides, supporting blood vessel maturation and osteogenesis. The early release of BMSCs and SKP, followed by the subsequent release of OGP and KLT, aligned with the dynamic process of bone regeneration. In a rat critical femoral condyle defect model, the BM-mimicking niche formed an in-situ ossification center, significantly enhancing bone regeneration. This study introduces a novel BM-mimicking niche characterized by a BMSC-enriched environment and the sequential release of therapeutic factors, offering a promising strategy for treating critical bone defects.
Bioactive MaterialsBiochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
28.00
自引率
6.30%
发文量
436
审稿时长
20 days
期刊介绍:
Bioactive Materials is a peer-reviewed research publication that focuses on advancements in bioactive materials. The journal accepts research papers, reviews, and rapid communications in the field of next-generation biomaterials that interact with cells, tissues, and organs in various living organisms.
The primary goal of Bioactive Materials is to promote the science and engineering of biomaterials that exhibit adaptiveness to the biological environment. These materials are specifically designed to stimulate or direct appropriate cell and tissue responses or regulate interactions with microorganisms.
The journal covers a wide range of bioactive materials, including those that are engineered or designed in terms of their physical form (e.g. particulate, fiber), topology (e.g. porosity, surface roughness), or dimensions (ranging from macro to nano-scales). Contributions are sought from the following categories of bioactive materials:
Bioactive metals and alloys
Bioactive inorganics: ceramics, glasses, and carbon-based materials
Bioactive polymers and gels
Bioactive materials derived from natural sources
Bioactive composites
These materials find applications in human and veterinary medicine, such as implants, tissue engineering scaffolds, cell/drug/gene carriers, as well as imaging and sensing devices.