An Immunomodulating Regenerating Hydrogel That Rescues the Oxidative Microenvironment and Reverses Cell Senescence for Osteoporotic Bone Defects
Open accessAbstract
Osteoporosis, which is characterized by reduced bone mass and structurally compromised bone tissue, along with aberrant levels of reactive oxygen species (ROS) and inflammation, has been a pressing clinical challenge. A large accumulation of ROS and pro-inflammatory factors can result in mitochondrial dysfunction and progressive cellular senescence, impeding efficacious regeneration of bone defects. Herein, in this work, a ROS-responsive hydrogel system containing HA-PBA coated Ce-ZOL nanocomposites (GHCZ) for excessive ROS scavenging and reversal of cellular senescence to accelerate bone regeneration in osteoporosis was designed and presented. The GHCZ hydrogel system allows for the sustained release of HA-PBA coated Ce-ZOL nanoparticles, which may scavenge the extracellular and intracellular ROS of BMSCs and macrophages through their prominent enzyme-like catalytic effect. Moreover, the GHCZ hydrogel system transforms the polarization phenotype of macrophages into anti-inflammation M2 type and inhibits pro-inflammatory cytokines. Meanwhile, it could reverse the senescence of BMSCs and apparently elevate their pro-osteogenic capacity through safeguarding mitochondrial function and reprograming the metabolic processes, ultimately promoting the healing of bone defects. Based on in vitro and in vivo results, powerful immunomodulation, favorable pro-inflammatory/oxidative microenvironment reshaping properties, desirable mitochondrial protection, and superior pro-osteogenic capacity of such a GHCZ hydrogel system display the profound effects on augmenting bone repair, which offers a paradigm for treating osteoporotic bone defects.
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References 42 · Cited by 43
- Authors
- Wang, W., Zhang, X., Zhang, L., Li, Z., Wang, L., Jiang, X., Wu, J., Zhou, L., Guo, Q., Huang, Y., Wang, W., Xi, K., Storm, G., Gu, Y., & Chen, L.
- Affiliations
- First Affiliated Hospital of Soochow University (CN)
- National University of Singapore (SG)
- Corresponding author
- Xi, Kun
- Storm, Gert
- Gu, Yong
- Chen, Liang
- ORCID
- Venue
- ACS Nano
- Publisher
- American Chemical Society (ACS)
- Published
- 2025-08-04
- Volume
- 19
- Issue
- 31
- Pages
- 28353-28371
- ISSN
- 1936-0851 (ISSN-L)
- 1936-086X
- OpenAlex
- W4412885438
- Cited by
- 43
- References
- 42
- Citations by year
- 2026: 37 · 2025: 6
- FWCI
- 10.42
- Type
- journal article
- Language
- en
- Open access
- green
- research.utwente.nl
- Licence
- Locations
- ACS Nano (publishedVersion)
- PubMed (publishedVersion)
- University of Twente Research Information (publishedVersion, other-oa)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- Funders
- Natural Science Foundation of Jiangsu Province (BK20211504, BK20230215)
- Project 333 of Jiangsu Province (2069999)
- National Natural Science Foundation of China (82072438, 82102589, 82120108017, 82272501, 82302683, 82372484)
- Priority Academic Program Development of Jiangsu Higher Education Institutions
- Jiangsu Innovative and Entrepreneurial Talent Program (JSSCBS20211570)
- Soochow University Medical + X project (ML12202923)
- Suzhou Gusu Health Talent Program (GSWS2021007, GSWS2021009)
- Medical Health Science and Technology Innovation Program of Suzhou (SKY2022119)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Keywords
- osteoporosis, bone defects, bone regeneration, hydrogels, reactive oxygen species scavenging, immunomodulation, macrophage polarization, M2 macrophages, bone marrow mesenchymal stem cells, mitochondrial dysfunction, cerium oxide nanoparticles, sustained drug release
- MeSH terms
- Animals, Bone Regeneration, Cerium, Humans, Macrophages, Osteogenesis, Osteoporosis, Cellular Senescence, Reactive Oxygen Species, Oxidative Stress, Hydrogels, Mice, Nanocomposites, Immunomodulation, Mesenchymal Stem Cells, Cellular Microenvironment
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