间充质干细胞的线粒体转移:揭示其机制和治疗潜力。

Jingyi Chen, Zhilang Xie, Huayin Zhou, Yingxin Ou, Wenwen Tan, Aizhen Zhang, Yuying Li, Xingliang Fan
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引用次数: 0

摘要

间充质干细胞(MSCs)由于其多样化的分化能力和再生特性,在转化医学中具有变革潜力。值得注意的是,MSCs可以通过细胞间线粒体转移将线粒体转移到不相关的细胞中,这为阻止线粒体疾病的进展和恢复因线粒体功能障碍而受损的细胞的功能提供了开创性的方法。尽管MSC线粒体转移已经在一系列疾病中显示出显著的治疗前景,但其在临床环境中的应用仍未得到很大的探索。这篇综述深入探讨了MSCs执行线粒体转移的新机制,强调了其对细胞代谢、免疫调节和组织再生的深远影响。我们对MSC线粒体转移的治疗潜力进行了深入分析,特别是在治疗线粒体功能障碍相关疾病和推进组织修复策略方面。此外,我们提出了在临床试验中优化MSC线粒体转移的创新考虑,强调其重塑再生医学和治疗干预前景的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondria Transfer in Mesenchymal Stem Cells: Unraveling the Mechanism and Therapeutic Potential.

Mesenchymal stem cells (MSCs) hold transformative potential in translational medicine due to their versatile differentiation abilities and regenerative properties. Notably, MSCs can transfer mitochondria to unrelated cells through intercellular mitochondrial transfer, offering a groundbreaking approach to halting the progression of mitochondrial diseases and restoring function to cells compromised by mitochondrial dysfunction. Although MSC mitochondrial transfer has demonstrated significant therapeutic promise across a range of diseases, its application in clinical settings remains largely unexplored. This review delves into the novel mechanisms by which MSCs execute mitochondrial transfer, highlighting its profound impact on cellular metabolism, immune modulation, and tissue regeneration. We provide an in-depth analysis of the therapeutic potential of MSC mitochondrial transfer, particularly in treating mitochondrial dysfunction-related diseases and advancing tissue repair strategies. Additionally, we propose innovative considerations for optimizing MSC mitochondrial transfer in clinical trials, emphasizing its potential to reshape the landscape of regenerative medicine and therapeutic interventions.

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