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开发轻度创伤性脑损伤的生物标志物:中枢神经系统来源外泌体的前景与进展

Developing Biomarkers of Mild Traumatic Brain Injury: Promise and Progress of CNS-Derived Exosomes.

作者信息

Vaughn Melonie N, Winston Charisse N, Levin Natalie, Rissman Robert A, Risbrough Victoria B

机构信息

Department of Neurosciences, University of California, San Diego, San Diego, CA, United States.

Veterans Affairs San Diego Health System, University of California, San Diego, San Diego, CA, United States.

出版信息

Front Neurol. 2022 Feb 10;12:698206. doi: 10.3389/fneur.2021.698206. eCollection 2021.

Abstract

Mild traumatic brain injuries (mTBI) are common injuries across civilian and military populations. Although most individuals recover after mTBI, some individuals continue to show long-term symptoms as well as increased risk for neurodegenerative and neuropsychiatric disorders. Currently, diagnosing TBI severity relies primarily on self-report and subjective symptoms, with limited tools for diagnosis or prognosis. Brain-derived exosomes, a form of extracellular vesicle, may offer a solution for interpreting injury states by aiding in diagnosis as well as outcome prediction with relatively low patient burden. Exosomes, which are released into circulation, contain both protein and RNA cargo that can be isolated and quantified, providing a molecular window into molecular status of the exosome source. Here we examined the current literature studying the utility of exosomes, in particular neuronal- and astrocyte-derived exosomes, to identify protein and miRNA biomarkers of injury severity, trajectory, and functional outcome. Current evidence supports the potential for these emerging new tools to capture an accessible molecular window into the brain as it responds to a traumatic injury, however a number of limitations must be addressed in future studies. Most current studies are relatively small and cross sectional; prospective, longitudinal studies across injury severity, and populations are needed to track exosome cargo changes after injury. Standardized exosome isolation as well as advancement in identifying/isolating exosomes from CNS-specific tissue sources will improve mechanistic understanding of cargo changes as well as reliability of findings. Exosomes are also just beginning to be used in model systems to understand functional effects of TBI-associated cargo such as toxicity. Finally linking exosome cargo changes to objective markers of neuronal pathology and cognitive changes will be critical in validating these tools to provide insights into injury and recovery states after TBI.

摘要

轻度创伤性脑损伤(mTBI)在平民和军人中都是常见的损伤。尽管大多数mTBI患者会康复,但一些患者仍会持续出现长期症状,以及神经退行性和神经精神性疾病风险增加。目前,诊断TBI严重程度主要依赖自我报告和主观症状,诊断或预后工具有限。脑源性外泌体是一种细胞外囊泡,可能为解释损伤状态提供一种解决方案,它有助于诊断和结果预测,且患者负担相对较低。释放到循环系统中的外泌体含有可分离和定量的蛋白质和RNA货物,为外泌体来源的分子状态提供了一个分子窗口。在这里,我们研究了当前关于外泌体效用的文献,特别是神经元和星形胶质细胞来源的外泌体,以确定损伤严重程度、病程和功能结果的蛋白质和miRNA生物标志物。目前的证据支持这些新兴的新工具有可能捕捉到大脑对创伤性损伤反应时可获取的分子窗口,然而,未来的研究必须解决一些局限性。目前大多数研究规模相对较小且为横断面研究;需要进行前瞻性、纵向研究,涵盖不同损伤严重程度和人群,以追踪损伤后外泌体货物的变化。标准化的外泌体分离以及从中枢神经系统特定组织来源识别/分离外泌体的进展将改善对货物变化的机制理解以及研究结果的可靠性。外泌体也刚刚开始用于模型系统,以了解TBI相关货物的功能影响,如毒性。最后,将外泌体货物变化与神经元病理学和认知变化的客观标志物联系起来,对于验证这些工具以深入了解TBI后的损伤和恢复状态至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9d0/8866179/90c9f86301c0/fneur-12-698206-g0001.jpg

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