间充质干细胞外泌体在脊髓损伤修复中的应用前景与挑战。

IF 2.2
Yifeng Zhang, Cunxin Zhang, Kai Gao, Kang Li, Maoqing Fu, Chaoliang Lv
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引用次数: 0

摘要

脊髓损伤(SCI)是一种严重的致残疾病,目前的治疗方法在很大程度上不足以恢复神经功能。尽管手术和药物干预取得了进展,但目前还没有有效的治疗方法来逆转脊髓损伤引起的神经功能缺损。间充质干细胞(MSCs),特别是人脐带来源的间充质干细胞(hucMSCs),由于其多能性和低免疫原性,在组织再生方面显示出前景。然而,诸如低植入率、致瘤性和潜在的免疫反应等挑战限制了它们的临床应用。近年来,间充质干细胞衍生外泌体(MSC-Exos)已成为一种有前景的治疗方法,在脊髓损伤治疗中显示出巨大的潜力。MSC-Exos通过免疫调节、促进血管生成和轴突再生、降低血脊髓屏障(BSCB)通透性等机制发挥其治疗作用。此外,hucMSC-Exos在可扩展性、安全性和治疗效果方面具有优势,使其成为一种有前途的无细胞修复方法。本文综述了MSC-Exos的生物学特性、在组织损伤修复中的作用及其在脊髓损伤病理生理不同阶段的机制贡献。了解这些机制将有助于为MSC-Exos作为一种新颖有效的脊髓损伤治疗策略的临床转化铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Application Prospects and Challenges of Mesenchymal Stem Cell-Derived Exosomes in Spinal Cord Injury Repair.

Spinal cord injury (SCI) is a severe, disabling condition for which current treatments are largely insufficient in restoring neurological function. Despite advances in surgical and pharmacological interventions, no effective treatment currently exists to reverse neurological deficits caused by SCI. Mesenchymal stem cells (MSCs), especially human umbilical cord-derived MSCs (hucMSCs), have shown promise in tissue regeneration due to their multipotency and low immunogenicity. However, challenges such as low engraftment rates, tumorigenicity, and potential immune responses limit their clinical application. In recent years, mesenchymal stem cell-derived exosomes (MSC-Exos) have emerged as a promising therapeutic approach, demonstrating significant potential in SCI treatment. MSC-Exos exerts its therapeutic effects through mechanisms such as immune modulation, promotion of angiogenesis and axon regeneration, and reduction of blood-spinal cord barrier (BSCB) permeability. Furthermore, hucMSC-Exos demonstrate advantages in scalability, safety, and therapeutic efficacy, making them a promising cell-free approach for SCI repair. This review summarizes the biological properties of MSC-Exos, their roles in tissue injury repair, and their mechanistic contributions across different phases of SCI pathophysiology. Understanding these mechanisms will help pave the way for clinical translation of MSC-Exos as a novel and effective therapeutic strategy for SCI.

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