Mesenchymal stem cell-derived extracellular vesicles in skin wound healing: roles, opportunities and challenges

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作者
Jia-Yi Ding
Min-Jiang Chen
Ling-Feng Wu
Gao-Feng Shu
Shi-Ji Fang
Zhao-Yu Li
Xu-Ran Chu
Xiao-Kun Li
Zhou-Guang Wang
Jian-Song Ji
机构
[1] the Fifth Affiliated Hospital of Wenzhou Medical University,Key Laboratory of Imaging Diagnosis and Minimally Invasive Intervention Research, Institute of Imaging Diagnosis and Minimally Invasive Intervention Research
[2] Wenzhou Medical University,Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision and Brain Health), School of Pharmaceutical Science
[3] Lishui University,Clinical College of the Affiliated Central Hospital, School of Medicine
[4] Jimei University,Department of Overseas Education College
[5] Justus-Liebig University Giessen,Department of Medicine II, Internal Medicine, Cardio
[6] Justus-Liebig University Giessen,Pulmonary Institute (CPI), Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL)
来源
关键词
Mesenchymal stem cell (MSC); Extracellular vesicles (EVs); Wound repair; Engineered nanoparticles;
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摘要
Skin wounds are characterized by injury to the skin due to trauma, tearing, cuts, or contusions. As such injuries are common to all human groups, they may at times represent a serious socioeconomic burden. Currently, increasing numbers of studies have focused on the role of mesenchymal stem cell (MSC)-derived extracellular vesicles (EVs) in skin wound repair. As a cell-free therapy, MSC-derived EVs have shown significant application potential in the field of wound repair as a more stable and safer option than conventional cell therapy. Treatment based on MSC-derived EVs can significantly promote the repair of damaged substructures, including the regeneration of vessels, nerves, and hair follicles. In addition, MSC-derived EVs can inhibit scar formation by affecting angiogenesis-related and antifibrotic pathways in promoting macrophage polarization, wound angiogenesis, cell proliferation, and cell migration, and by inhibiting excessive extracellular matrix production. Additionally, these structures can serve as a scaffold for components used in wound repair, and they can be developed into bioengineered EVs to support trauma repair. Through the formulation of standardized culture, isolation, purification, and drug delivery strategies, exploration of the detailed mechanism of EVs will allow them to be used as clinical treatments for wound repair. In conclusion, MSC-derived EVs-based therapies have important application prospects in wound repair. Here we provide a comprehensive overview of their current status, application potential, and associated drawbacks.
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