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细胞外囊泡在创伤性脑损伤诊断和治疗中的临床应用。

Clinical Applications of Extracellular Vesicles in the Diagnosis and Treatment of Traumatic Brain Injury.

机构信息

Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Department of Neurosurgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

出版信息

J Neurotrauma. 2020 Oct 1;37(19):2045-2056. doi: 10.1089/neu.2020.6990. Epub 2020 Jun 2.

DOI:10.1089/neu.2020.6990
PMID:32312151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7502684/
Abstract

Extracellular vesicles (EVs) have emerged as key mediators of cell-cell communication during homeostasis and in pathology. Central nervous system (CNS)-derived EVs contain cell type-specific surface markers and intralumenal protein, RNA, DNA, and metabolite cargo that can be used to assess the biochemical and molecular state of neurons and glia during neurological injury and disease. The development of EV isolation strategies coupled with analysis of multi-plexed biomarker and clinical data have the potential to improve our ability to classify and treat traumatic brain injury (TBI) and resulting sequelae. Additionally, their ability to cross the blood-brain barrier (BBB) has implications for both EV-based diagnostic strategies and for potential EV-based therapeutics. In the present review, we discuss encouraging data for EV-based diagnostic, prognostic, and therapeutic strategies in the context of TBI monitoring and management.

摘要

细胞外囊泡 (EVs) 在稳态和病理过程中成为细胞间通讯的关键介质。中枢神经系统 (CNS) 来源的 EVs 包含细胞类型特异性的表面标志物和管腔内蛋白、RNA、DNA 和代谢物货物,可用于评估神经损伤和疾病期间神经元和神经胶质的生化和分子状态。EV 分离策略的发展以及对多指标生物标志物和临床数据的分析有可能提高我们对创伤性脑损伤 (TBI) 及其后果进行分类和治疗的能力。此外,它们穿过血脑屏障 (BBB) 的能力对基于 EV 的诊断策略和潜在的基于 EV 的治疗都有影响。在本综述中,我们讨论了基于 EV 的诊断、预后和治疗策略在 TBI 监测和管理方面的令人鼓舞的数据。

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本文引用的文献

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Traumatic brain injury increases plasma astrocyte-derived exosome levels of neurotoxic complement proteins.创伤性脑损伤增加了血浆星形胶质细胞衍生的外泌体中神经毒性补体蛋白的水平。
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Brain-Immune Interactions and Neuroinflammation After Traumatic Brain Injury.创伤性脑损伤后的脑-免疫相互作用与神经炎症
Front Neurosci. 2019 Nov 12;13:1178. doi: 10.3389/fnins.2019.01178. eCollection 2019.
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EK7 Regulates NLRP3 Inflammasome Activation and Neuroinflammation Post-traumatic Brain Injury.EK7调节创伤性脑损伤后的NLRP3炎性小体激活和神经炎症。
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Profiling of Exosomal Biomarkers for Accurate Cancer Identification: Combining DNA-PAINT with Machine- Learning-Based Classification.外泌体生物标志物在癌症精准识别中的分析:DNA-PAINT 与基于机器学习的分类相结合。
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Microfluidic Technology for Clinical Applications of Exosomes.用于外泌体临床应用的微流控技术
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Increases in miR-124-3p in Microglial Exosomes Confer Neuroprotective Effects by Targeting FIP200-Mediated Neuronal Autophagy Following Traumatic Brain Injury.小胶质细胞外泌体中 miR-124-3p 的增加通过靶向创伤性脑损伤后 FIP200 介导的神经元自噬发挥神经保护作用。
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Multi-Dimensional Mapping of Brain-Derived Extracellular Vesicle MicroRNA Biomarker for Traumatic Brain Injury Diagnostics.用于创伤性脑损伤诊断的脑源性细胞外囊泡 microRNA 生物标志物的多维映射。
J Neurotrauma. 2020 Nov 15;37(22):2424-2434. doi: 10.1089/neu.2018.6220. Epub 2019 May 6.
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MiR-124 Enriched Exosomes Promoted the M2 Polarization of Microglia and Enhanced Hippocampus Neurogenesis After Traumatic Brain Injury by Inhibiting TLR4 Pathway.miR-124 富集的外泌体通过抑制 TLR4 通路促进创伤性脑损伤后小胶质细胞的 M2 极化和增强海马神经发生。
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Altered levels of plasma neuron-derived exosomes and their cargo proteins characterize acute and chronic mild traumatic brain injury.血浆神经元衍生外泌体及其货物蛋白水平的改变可用于急性和慢性轻度创伤性脑损伤的特征化诊断。
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