Mesenchymal stem cells and mesenchymal stem cell-derived exosomes: a promising strategy for treating retinal degenerative diseases.

IF 6.4 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Medicine Pub Date : 2025-02-21 DOI:10.1186/s10020-025-01120-w
Wenjing An, Wenliang Zhang, Jia Qi, Weihui Xu, Yushan Long, Huan Qin, Kai Yao
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Abstract

Mesenchymal stem cells (MSCs) have emerged as a promising therapeutic strategy in regenerative medicine, demonstrating significant potential for clinical applications. Evidence suggests that MSCs not only exhibit multipotent differentiation potential but also exert critical therapeutic effects in retinal degenerative diseases via robust paracrine mechanisms. MSCs protect retinal cells from degenerative damage by modulating inflammation, inhibiting apoptosis, alleviating oxidative stress, and suppressing cell death pathways. Furthermore, MSCs contribute to retinal structural and functional stability by facilitating vascular remodeling and donating mitochondria to retinal cells. Of particular interest, MSC-derived exosomes have gained widespread attention as a compelling cell-free therapy. Owing to their potent anti-inflammatory, anti-apoptotic, and vascular-stabilizing properties, exosomes show significant promise for the treatment of retinal degenerative diseases.

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间充质干细胞和间充质干细胞衍生的外泌体:一种治疗视网膜退行性疾病的有希望的策略。
间充质干细胞(MSCs)在再生医学中已成为一种很有前景的治疗策略,显示出巨大的临床应用潜力。有证据表明,MSCs不仅表现出多能分化潜能,而且通过强大的旁分泌机制在视网膜退行性疾病中发挥关键的治疗作用。MSCs通过调节炎症、抑制细胞凋亡、减轻氧化应激和抑制细胞死亡途径来保护视网膜细胞免受退行性损伤。此外,MSCs通过促进血管重塑和向视网膜细胞提供线粒体来促进视网膜结构和功能的稳定。特别有趣的是,msc衍生的外泌体作为一种引人注目的无细胞疗法已经获得了广泛的关注。由于其有效的抗炎、抗细胞凋亡和血管稳定特性,外泌体在视网膜退行性疾病的治疗中显示出显著的前景。
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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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