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用于脊髓损伤的载有外泌体的生物支架:综述

Exosome-Loaded Bioscaffolds for Spinal Cord Injuries: A Review.

作者信息

Chen Ruilin, Zheng Jian, Hao Jie, Yang Yang, Xu Shaohu, Zhang Feiyu, Zhang Feng, Yao Yu

机构信息

School of Medicine, Nantong University, Nantong, Jiangsu Province 226001, China.

Department of Orthopedics, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province 226001, China.

出版信息

Stem Cells Int. 2025 Jul 30;2025:8841129. doi: 10.1155/sci/8841129. eCollection 2025.


DOI:10.1155/sci/8841129
PMID:40771301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12328054/
Abstract

Exosomes are naturally occurring cellular products released by various cell types in the body. Their composition is similar to that of human tissues, which reduces the risk of immune rejection. As critical mediators of intercellular communication, exosomes transmit signals and information that regulate the physiological states of surrounding tissues. Depending on their cellular origin and molecular content, exosomes can either promote nerve regeneration and functional recovery at the site of spinal cord injury (SCI) or exacerbate the local injury microenvironment. However, as a cellular product, the composition and function of exosomes are affected by the type and state of the cells from which they originate, and thus, there may be specificity problems in treatment, such as the possible instability of the therapeutic effect, et cetera. Moreover, exosomes need to be further optimized in terms of their delivery and release strategies in order to improve the duration and stability of the therapeutic effect. Thus, a single therapy approach is often insufficient to effectively support nerve repair following SCI. Numerous studies have demonstrated that encapsulating exosomes within biomaterial scaffolds enhances their delivery and retention at the injury site, thereby improving their viability. This paper reviews the latest research on stem cell-derived exosomes and biomaterials in the context of SCI. It further explores the combined application of exosomes and biomaterial scaffolds in SCI treatment, while also addressing the associated challenges and future prospects.

摘要

外泌体是体内各种细胞类型释放的天然细胞产物。它们的组成与人体组织相似,这降低了免疫排斥的风险。作为细胞间通讯的关键介质,外泌体传递调节周围组织生理状态的信号和信息。根据其细胞来源和分子含量,外泌体既可以促进脊髓损伤(SCI)部位的神经再生和功能恢复,也可以加剧局部损伤微环境。然而,作为一种细胞产物,外泌体的组成和功能受其来源细胞的类型和状态影响,因此在治疗中可能存在特异性问题,如治疗效果可能不稳定等。此外,外泌体在递送和释放策略方面需要进一步优化,以提高治疗效果的持续时间和稳定性。因此,单一的治疗方法往往不足以有效支持SCI后的神经修复。大量研究表明,将外泌体包裹在生物材料支架中可增强其在损伤部位的递送和保留,从而提高其存活率。本文综述了在SCI背景下干细胞来源的外泌体和生物材料的最新研究。它进一步探讨了外泌体与生物材料支架在SCI治疗中的联合应用,同时也讨论了相关挑战和未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e42/12328054/4608bbb7d128/SCI2025-8841129.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e42/12328054/09577acd0322/SCI2025-8841129.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e42/12328054/9e27c0a5e343/SCI2025-8841129.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e42/12328054/4608bbb7d128/SCI2025-8841129.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e42/12328054/09577acd0322/SCI2025-8841129.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e42/12328054/9e27c0a5e343/SCI2025-8841129.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e42/12328054/4608bbb7d128/SCI2025-8841129.003.jpg

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Exosome-Loaded Bioscaffolds for Spinal Cord Injuries: A Review.

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本文引用的文献

[1]
Comparative analysis of the minimal information for studies of extracellular vesicles guidelines: Advancements and implications for extracellular vesicle research.

Semin Cancer Biol. 2024-6

[2]
BMSCs-derived exosomes inhibit macrophage/microglia pyroptosis by increasing autophagy through the miR-21a-5p/PELI1 axis in spinal cord injury.

Aging (Albany NY). 2024-3-11

[3]
M2 Microglia-derived Exosomes Promote Spinal Cord Injury Recovery in Mice by Alleviating A1 Astrocyte Activation.

Mol Neurobiol. 2024-9

[4]
M2 microglia-derived exosome-loaded electroconductive hydrogel for enhancing neurological recovery after spinal cord injury.

J Nanobiotechnology. 2024-1-3

[5]
Local delivery of EGFRNSCs-derived exosomes promotes neural regeneration post spinal cord injury via miR-34a-5p/HDAC6 pathway.

Bioact Mater. 2023-11-28

[6]
Pericyte-derived exosomal miR-210 improves mitochondrial function and inhibits lipid peroxidation in vascular endothelial cells after traumatic spinal cord injury by activating JAK1/STAT3 signaling pathway.

J Nanobiotechnology. 2023-11-27

[7]
Exosomes derived from human placental mesenchymal stem cells in combination with hyperbaric oxygen synergically alleviates spinal cord ischemia-reperfusion injury.

Regen Ther. 2023-9-13

[8]
Thermos-responsive hydrogel system encapsulated engineered exosomes attenuate inflammation and oxidative damage in acute spinal cord injury.

Front Bioeng Biotechnol. 2023-8-8

[9]
Umbilical mesenchymal stem cell-derived exosomes promote spinal cord functional recovery through the miR-146b/TLR4 -mediated NF-κB p65 signaling pathway in rats.

Biochem Biophys Rep. 2023-7-20

[10]
Current Concepts of Biomaterial Scaffolds and Regenerative Therapy for Spinal Cord Injury.

Int J Mol Sci. 2023-1-28

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