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脂肪来源干细胞外泌体中的非编码RNA:伤口愈合的机制、治疗潜力及挑战

Non-coding RNAs in adipose-derived stem cell exosomes: Mechanisms, therapeutic potential, and challenges in wound healing.

作者信息

Rong Jian, Li Yao-Yao, Wang Xin, Wang Jia-Ning, Song Mei

机构信息

Department of Burns and Plastic Surgery, The 940 Hospital of Joint Logistics Support Force of Chinese People's Liberation Army, Lanzhou 730050, Gansu Province, China.

Department of Plateau Medicine, The 940 Hospital of Joint Logistics Support Force of Chinese People's Liberation Army, Lanzhou 730050, Gansu Province, China.

出版信息

World J Stem Cells. 2025 Apr 26;17(4):102917. doi: 10.4252/wjsc.v17.i4.102917.

DOI:10.4252/wjsc.v17.i4.102917
PMID:40308889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12038460/
Abstract

The treatment of complex wounds presents a significant clinical challenge due to the limited availability of standardized therapeutic options. Adipose-derived stem cell exosomes (ADSC-Exos) are promising for their capabilities to enhance angiogenesis, mitigate oxidative stress, modulate inflammatory pathways, support skin cell regeneration, and promote epithelialization. These exosomes deliver non-coding RNAs, including microRNAs, long non-coding RNAs, and circular RNAs, which facilitate collagen remodeling, reduce scar formation, and expedite wound healing. This study reviews the mechanisms, therapeutic roles, and challenges of non-coding RNA-loaded ADSC-Exos in wound healing and identifies critical directions for future research. It aims to provide insights for researchers into the potential mechanisms and clinical applications of ADSC-Exos non-coding RNAs in wound healing.

摘要

由于标准化治疗方案有限,复杂伤口的治疗面临重大临床挑战。脂肪来源干细胞外泌体(ADSC-Exos)因其具有促进血管生成、减轻氧化应激、调节炎症途径、支持皮肤细胞再生和促进上皮形成的能力而颇具前景。这些外泌体携带非编码RNA,包括微小RNA、长链非编码RNA和环状RNA,它们有助于胶原蛋白重塑、减少瘢痕形成并加速伤口愈合。本研究综述了负载非编码RNA的ADSC-Exos在伤口愈合中的作用机制、治疗作用和挑战,并确定了未来研究的关键方向。其目的是为研究人员提供有关ADSC-Exos非编码RNA在伤口愈合中的潜在机制和临床应用的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/ac72c945adfc/102917-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/882b6461a883/102917-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/4770c5326449/102917-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/99507b3f3f8d/102917-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/ac72c945adfc/102917-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/882b6461a883/102917-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/4770c5326449/102917-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/99507b3f3f8d/102917-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/12038460/ac72c945adfc/102917-g004.jpg

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本文引用的文献

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Tissue Cell. 2024 Dec;91:102575. doi: 10.1016/j.tice.2024.102575. Epub 2024 Oct 1.
2
Exosomal miR‑194 from adipose‑derived stem cells impedes hypertrophic scar formation through targeting TGF‑β1.脂肪来源干细胞外泌体 miR-194 通过靶向 TGF-β1 抑制增生性瘢痕形成。
Mol Med Rep. 2024 Dec;30(6). doi: 10.3892/mmr.2024.13340. Epub 2024 Sep 27.
3
NORAD accelerates skin wound healing through extracellular vesicle transfer from hypoxic adipose derived stem cells: miR-524-5p pathway and Pumilio protein mechanism.
NORAD 通过缺氧脂肪来源干细胞的细胞外囊泡转移加速皮肤伤口愈合:miR-524-5p 通路和 Pumilio 蛋白机制。
Int J Biol Macromol. 2024 Nov;279(Pt 4):135621. doi: 10.1016/j.ijbiomac.2024.135621. Epub 2024 Sep 12.
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Bilayer hydrogel with a protective film and a regenerative hydrogel for effective diabetic wound treatment.具有保护膜的双层水凝胶和再生水凝胶,可有效治疗糖尿病伤口。
Biomater Sci. 2024 Sep 25;12(19):5036-5051. doi: 10.1039/d4bm00547c.
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