Polyethylene glycol-polyester based temperature-sensitive hydrogel delivering mesenchymal stem cell-derived exosomes enhances acute skin wound healing

伤口愈合 间充质干细胞 外体 成纤维细胞 微泡 脐静脉 肉芽组织 肌成纤维细胞 化学 伤口闭合 生物相容性 医学 血管生成 真皮 生物医学工程 细胞外基质 真皮成纤维细胞 再生医学 纤维化 纤维蛋白 药物输送 炎症 病理 干细胞 止血 人体皮肤 细胞疗法 细胞迁移
作者
Zining Wei,Jie Ren,Jianshe Hu,Haiming Wei
出处
期刊:Frontiers in Bioengineering and Biotechnology [Frontiers Media]
卷期号:13
标识
DOI:10.3389/fbioe.2025.1730631
摘要

Skin wound healing remains a significant clinical challenge. Conventional dressings have limitations in maintaining an optimal wound microenvironment and preventing secondary injury. In this study, we developed a Poly (lactic-co-glycolic acid)-poly (ethylene glycol)-poly (lactic-co-glycolic acid) (PLGA-PEG-PLGA, PPP) thermosensitive hydrogel loaded with mesenchymal stem cell-derived exosomes (MSC-Exos) to enhance acute skin wound healing by prolonging exosome retention and bioavailability at the wound site. The hydrogel exhibited a rapid sol-gel transition at approximately 32 °C, demonstrating good mechanical stability (storage modulus (G′) > loss modulus (G″)) and self-healing properties at physiological temperature. In vitro experiments revealed that PPP/Exos showed superior biocompatibility with L929 mouse fibroblast cells (L929 cells) and human umbilical vein endothelial cells (HUVECs), significantly promoting cell proliferation and vascular tube formation. In a Sprague-Dawley (SD) rat full-thickness skin defect model, the PPP/Exos group markedly accelerated wound closure. By day 14, wound closure reached 98.6% in the PPP/Exos group, compared with 87.6% in the control group. Histopathological examination further revealed that PPP/Exos treatment effectively enhanced granulation tissue formation, attenuated inflammatory responses, facilitated re-epithelialization, and substantially increased collagen deposition. Through immunohistochemical analysis, we identified three mechanisms underlying the enhanced wound healing: promoted angiogenesis, accelerated myofibroblast differentiation, and reduced inflammation. Collectively, the PPP/Exos thermosensitive hydrogel, with its excellent biocompatibility, injectability, and sustained exosome release characteristics, significantly promotes wound healing through synergistic “angiogenesis-tissue remodeling-anti-inflammation” effects. This system offers a promising therapeutic strategy for clinical wound management and establishes a solid foundation for applications in regenerative medicine.
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