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间充质干细胞来源的外泌体:治疗缺血性中风的新作用

Exosomes Derived From Mesenchymal Stem Cells: Novel Effects in the Treatment of Ischemic Stroke.

作者信息

Xiong Yu, Song Jianping, Huang Xinyue, Pan Zhigang, Goldbrunner Roland, Stavrinou Lampis, Lin Shu, Hu Weipeng, Zheng Feng, Stavrinou Pantelis

机构信息

Department of Neurosurgery, The Second Affiliated Hospital, Fujian Medical University, Quanzhou, China.

Department of Neurosurgery, Shanghai Medical College, Huashan Hospital, Fudan University, Shanghai, China.

出版信息

Front Neurosci. 2022 May 2;16:899887. doi: 10.3389/fnins.2022.899887. eCollection 2022.

Abstract

Ischemic stroke is defined as an infarction in the brain, caused by impaired cerebral blood supply, leading to local brain tissue ischemia, hypoxic necrosis, and corresponding neurological deficits. At present, revascularization strategies in patients with acute ischemic stroke include intravenous thrombolysis and mechanical endovascular treatment. However, due to the short treatment time window (<4.5 h) and method restrictions, clinical research is focused on new methods to treat ischemic stroke. Exosomes are nano-sized biovesicles produced in the endosomal compartment of most eukaryotic cells, containing DNA, complex RNA, and protein (30-150 nm). They are released into surrounding extracellular fluid upon fusion between multivesicular bodies and the plasma membrane. Exosomes have the characteristics of low immunogenicity, good innate stability, high transmission efficiency, and the ability to cross the blood-brain barrier, making them potential therapeutic modalities for the treatment of ischemic stroke. The seed sequence of miRNA secreted by exosomes is base-paired with complementary mRNA to improve the microenvironment of ischemic tissue, thereby regulating downstream signal transduction activities. With exosome research still in the theoretical and experimental stages, this review aims to shed light on the potential of exosomes derived from mesenchymal stem cells in the treatment of ischemic stroke.

摘要

缺血性中风被定义为脑部梗死,由脑供血受损引起,导致局部脑组织缺血、缺氧坏死及相应的神经功能缺损。目前,急性缺血性中风患者的血管再通策略包括静脉溶栓和机械性血管内治疗。然而,由于治疗时间窗短(<4.5小时)及方法限制,临床研究聚焦于治疗缺血性中风的新方法。外泌体是大多数真核细胞内体区室产生的纳米级生物囊泡,包含DNA、复杂RNA和蛋白质(30 - 150纳米)。它们在多泡体与质膜融合后释放到周围细胞外液中。外泌体具有低免疫原性、良好的固有稳定性、高传递效率及穿越血脑屏障的能力,使其成为治疗缺血性中风的潜在治疗方式。外泌体分泌的miRNA种子序列与互补mRNA碱基配对,以改善缺血组织的微环境,从而调节下游信号转导活动。鉴于外泌体研究仍处于理论和实验阶段,本综述旨在阐明间充质干细胞来源的外泌体在治疗缺血性中风方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7cd/9108502/ae657e12610c/fnins-16-899887-g001.jpg

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