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富含特定微小RNA的工程化外泌体可增强其对创伤性脑损伤和中风的治疗效果。

Engineered exosomes enriched with select microRNAs amplify their therapeutic efficacy for traumatic brain injury and stroke.

作者信息

Chen Liang, Xiong Ye, Chopp Michael, Zhang Yanlu

机构信息

Department of Neurosurgery, Henry Ford Health, Detroit, MI, United States.

Department of Neurology, Henry Ford Health, Detroit, MI, United States.

出版信息

Front Cell Neurosci. 2024 Mar 19;18:1376601. doi: 10.3389/fncel.2024.1376601. eCollection 2024.

DOI:10.3389/fncel.2024.1376601
PMID:38566841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10985177/
Abstract

Traumatic brain injury (TBI) and stroke stand as prominent causes of global disability and mortality. Treatment strategies for stroke and TBI are shifting from targeting neuroprotection toward cell-based neurorestorative strategy, aiming to augment endogenous brain remodeling, which holds considerable promise for the treatment of TBI and stroke. Compelling evidence underscores that the therapeutic effects of cell-based therapy are mediated by the active generation and release of exosomes from administered cells. Exosomes, endosomal derived and nano-sized extracellular vesicles, play a pivotal role in intercellular communication. Thus, we may independently employ exosomes to treat stroke and TBI. Systemic administration of mesenchymal stem cell (MSC) derived exosomes promotes neuroplasticity and neurological functional recovery in preclinical animal models of TBI and stroke. In this mini review, we describe the properties of exosomes and recent exosome-based therapies of TBI and stroke. It is noteworthy that the microRNA cargo within exosomes contributes to their therapeutic effects. Thus, we provide a brief introduction to microRNAs and insight into their key roles in mediating therapeutic effects. With the increasing knowledge of exosomes, researchers have "engineered" exosome microRNA content to amplify their therapeutic benefits. We therefore focus our discussion on the therapeutic benefits of recently employed microRNA-enriched engineered exosomes. We also discuss the current opportunities and challenges in translating exosome-based therapy to clinical applications.

摘要

创伤性脑损伤(TBI)和中风是导致全球残疾和死亡的主要原因。中风和TBI的治疗策略正从靶向神经保护转向基于细胞的神经修复策略,旨在增强内源性脑重塑,这为TBI和中风的治疗带来了巨大希望。有力证据表明,基于细胞的治疗效果是由给药细胞主动产生和释放外泌体介导的。外泌体是源自内体的纳米级细胞外囊泡,在细胞间通讯中起关键作用。因此,我们可以单独使用外泌体来治疗中风和TBI。在TBI和中风的临床前动物模型中,全身给予间充质干细胞(MSC)衍生的外泌体可促进神经可塑性和神经功能恢复。在本综述中,我们描述了外泌体的特性以及最近基于外泌体的TBI和中风治疗方法。值得注意的是,外泌体内的微小RNA成分有助于其治疗效果。因此,我们简要介绍了微小RNA,并深入探讨了它们在介导治疗效果中的关键作用。随着对外泌体认识的不断增加,研究人员已经“设计”了外泌体微小RNA含量以增强其治疗益处。因此,我们将讨论重点放在最近使用的富含微小RNA的工程化外泌体的治疗益处上。我们还讨论了将基于外泌体的治疗转化为临床应用的当前机遇和挑战。

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Front Cell Neurosci. 2024 Mar 19;18:1376601. doi: 10.3389/fncel.2024.1376601. eCollection 2024.
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本文引用的文献

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The Role of Microglial Exosomes and miR-124-3p in Neuroinflammation and Neuronal Repair after Traumatic Brain Injury.小胶质细胞外泌体和miR-124-3p在创伤性脑损伤后神经炎症和神经元修复中的作用
Life (Basel). 2023 Sep 16;13(9):1924. doi: 10.3390/life13091924.
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Mesenchymal stem cell secretome and extracellular vesicles for neurodegenerative diseases: Risk-benefit profile and next steps for the market access.用于神经退行性疾病的间充质干细胞分泌组和细胞外囊泡:风险效益概况及市场准入的下一步措施
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NSC-derived exosomes enhance therapeutic effects of NSC transplantation on cerebral ischemia in mice.NSC 来源的外泌体增强 NSC 移植对小鼠脑缺血的治疗效果。
Elife. 2023 Apr 27;12:e84493. doi: 10.7554/eLife.84493.
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Bone marrow stromal cells-derived exosomes reduce neurological damage in traumatic brain injury through the miR-124-3p/p38 MAPK/GLT-1 axis.骨髓基质细胞衍生的外泌体通过 miR-124-3p/p38MAPK/GLT-1 轴减轻创伤性脑损伤的神经损伤。
Exp Neurol. 2023 Jul;365:114408. doi: 10.1016/j.expneurol.2023.114408. Epub 2023 Apr 13.
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Extracellular Vesicles Derived From Neural Stem Cells, Astrocytes, and Microglia as Therapeutics for Easing TBI-Induced Brain Dysfunction.神经干细胞、星形胶质细胞和小胶质细胞来源的细胞外囊泡作为治疗外伤性脑损伤引起的脑功能障碍的方法。
Stem Cells Transl Med. 2023 Mar 17;12(3):140-153. doi: 10.1093/stcltm/szad004.
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