ADSC-derived exosomes deliver cerium oxide nanoparticles to promote diabetic wound healing via anti-inflammatory and pro-angiogenic effects

Diabetic wounds pose a significant clinical challenge due to excessive oxidative stress, chronic inflammation, and impaired angiogenesis. To address these issues, this study developed a novel nanocomposite, CeO<sub>2</sub>@Exo, by loading cerium oxide nanoparticles (CeO<sub>2</sub> NPs) into adipose-derived stem cell-derived exosomes. In both <i>in vitro</i> and <i>in vivo</i> diabetic models, CeO<sub>2</sub>@Exo effectively scavenged reactive oxygen species, promoted VEGF-mediated angiogenesis, and accelerated wound closure. Importantly, it modulated the inflammatory microenvironment by shifting macrophage polarization from the pro-inflammatory M1 to the pro-regenerative M2 phenotype, thereby enhancing the release of anti-inflammatory cytokines. These multifunctional effects demonstrate that CeO<sub>2</sub>@Exo represents a promising, comprehensive therapeutic strategy for diabetic wound healing, overcoming the limitations of conventional single-target treatments.

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Publication Details

Journal
iScience
Published
2025-12-31
DOI
https://doi.org/10.1016/j.isci.2025.114560
Primary Topic
Extracellular vesicles in disease
Type
article
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article

ADSC-derived exosomes deliver cerium oxide nanoparticles to promote diabetic wound healing via anti-inflammatory and pro-angiogenic effects

Yichao Huang, Yuanpeng Nie, Yucheng Zhang, Lei Cao et al.
iScience
Extracellular vesicles in disease
article

ADSC-derived exosomes deliver cerium oxide nanoparticles to promote diabetic wound healing via anti-inflammatory and pro-angiogenic effects

Yichao Huang, Yuanpeng Nie, Yucheng Zhang, Lei Cao, Yu Zeng, Tao Yu, Qingyan Li, Tong Peng
article en

Abstract

Diabetic wounds pose a significant clinical challenge due to excessive oxidative stress, chronic inflammation, and impaired angiogenesis. To address these issues, this study developed a novel nanocomposite, CeO<sub>2</sub>@Exo, by loading cerium oxide nanoparticles (CeO<sub>2</sub> NPs) into adipose-derived stem cell-derived exosomes. In both <i>in vitro</i> and <i>in vivo</i> diabetic models, CeO<sub>2</sub>@Exo effectively scavenged reactive oxygen species, promoted VEGF-mediated angiogenesis, and accelerated wound closure. Importantly, it modulated the inflammatory microenvironment by shifting macrophage polarization from the pro-inflammatory M1 to the pro-regenerative M2 phenotype, thereby enhancing the release of anti-inflammatory cytokines. These multifunctional effects demonstrate that CeO<sub>2</sub>@Exo represents a promising, comprehensive therapeutic strategy for diabetic wound healing, overcoming the limitations of conventional single-target treatments.

iScienceVol. 29(2)
Sun Yat-sen University (CN), Longgang Central Hospital (CN), The Seventh Affiliated Hospital of Sun Yat-sen University (CN), ShenZhen People’s Hospital (CN), Shenzhen Bao'an District People's Hospital (CN)
Openalex Percentile: Top 35%
Extracellular vesicles in disease
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