脑类器官释放的细胞外囊泡和miRNA的表征

IF 2.9 Q2 TOXICOLOGY
Brian B. Silver , Rick Fannin , Kevin Gerrish , Erik J. Tokar
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引用次数: 0

摘要

环境毒物可导致几种神经退行性疾病的发展。然而,这种病理背后的机制仍然不完全清楚。及时诊断即将发生的神经变性对于早期干预以防止认知能力下降至关重要。为此,需要准确的早期神经退行性过程和暴露风险的生物标志物。细胞外囊泡(EVs)是细胞释放的脂质颗粒,含有许多生物活性分子,包括mirna。电动汽车既可以作为传播神经毒性表型的途径,也可以作为神经系统疾病生物标志物的来源。然而,电动汽车传播有毒物质有害影响的确切机制以及它们作为生物标志物的全部用途仍不清楚。类器官模型有几个优点,包括在高通量毒物测试和个性化医学和疾病模型中的应用潜力。然而,很少有研究检测EV在脑类器官中的释放,以确定EV是否含有有用的生物标志物。我们采用了几种技术来表征人脑类器官及其相关mirna释放的ev。我们发现脑类器官持续释放ev相关的miRNA,其数量足以用NanoString进行稳健分析。此外,通路分析显示,与神经退行性疾病和神经系统信号相关的术语与恢复的mirna相关。综上所述,这些数据表明,脑类器官可作为发现参与神经退行性疾病和神经毒性的ev相关mirna的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Characterization of extracellular vesicles and miRNA released by cerebral organoids

Characterization of extracellular vesicles and miRNA released by cerebral organoids
Environmental toxicants can contribute to the development of several neurodegenerative diseases. However, the mechanisms behind this pathology are still incompletely understood. Prompt diagnosis of impending neurodegeneration is crucial for early interventions to prevent cognitive decline. Towards this end, accurate biomarkers for early neurodegenerative processes and exposure risk are needed. Extracellular vesicles (EVs) are lipid particles released by cells which contain many bioactive molecules including miRNAs. EVs may serve both as a route of propagating neurotoxic phenotypes and as a source of biomarkers for neurological disease. However, the exact mechanisms though which EVs could spread the deleterious effects of toxicants and the full spectrum of their usage as biomarkers remain unclear. Organoid models have several advantages, including potential for use in high-throughput toxicant testing and applications in personalized medicine and disease models. However, few studies have examined EV release in brain organoids to determine if the EVs could contain useful biomarkers. We employed several technologies to characterize EVs released by human cerebral organoids and their associated miRNAs. We identified that cerebral organoids consistently release EV-associated miRNA in quantities sufficient for robust analysis with NanoString. Further, pathway analyses revealed that terms related to neurodegenerative disease and nervous system signaling are associated with the recovered miRNAs. Together, these data suggest that cerebral organoids have utility as a tool for the discovery of EV-associated miRNAs involved in neurodegenerative disease and neurotoxicity.
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来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
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