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鉴定 YWHAH 作为一种新型的脑源性细胞外囊泡标志物在后长期咪达唑仑暴露于早期发育期间。

Identification of YWHAH as a Novel Brain-Derived Extracellular Vesicle Marker Post Long-Term Midazolam Exposure during Early Development.

机构信息

Department of Anesthesiology, University of Nebraska Medical Center (UNMC), Omaha, NE 68198, USA.

Department of Genetics, Cell Biology, and Anatomy, University of Nebraska Medical Center (UNMC), Omaha, NE 68198, USA.

出版信息

Cells. 2023 Mar 22;12(6):966. doi: 10.3390/cells12060966.

Abstract

Recently, the long-term use of sedative agents in the neonatal intensive care unit (NICU) has raised concerns about neurodevelopmental outcomes in exposed neonates. Midazolam (MDZ), a common neonatal sedative in the NICU, has been suggested to increase learning disturbances and cognitive impairment in children. However, molecular mechanisms contributing to such outcomes with long-term MDZ use during the early stages of life remain unclear. In this study, we for the first time elucidate the role of brain-derived extracellular vesicles (BDEVs), including mining the BDEV proteome post long-term MDZ exposure during early development. Employing our previously established rodent model system that mimics the exposure of MDZ in the NICU using an increasing dosage regimen, we isolated BDEVs from postnatal 21-days-old control and MDZ groups using a differential sucrose density gradient. BDEVs from the control and MDZ groups were then characterized using a ZetaView nanoparticle tracking analyzer and transmission electron microscopy analysis. Next, using RT-qPCR, we examined the expression of key ESCRT-related genes involved in EV biogenesis. Lastly, using quantitative mass spectrometry-based proteomics, we mined the BDEV protein cargo that revealed key differentially expressed proteins and associated molecular pathways to be altered post long-term MDZ exposure. Our study characterized the proteome in BDEV cargo from long-term MDZ exposure at early development. Importantly, we identified and validated the expression of YWHAH as a potential target for further characterization of its downstream mechanism and a potential biomarker for the early onset of neurodevelopment and neurodegenerative diseases. Overall, the present study demonstrated long-term exposure to MDZ at early development stages could influence BDEV protein cargo, which potentially impact neural functions and behavior at later stages of development.

摘要

最近,新生儿重症监护病房(NICU)中镇静剂的长期使用引起了人们对暴露于镇静剂的新生儿神经发育结局的关注。咪达唑仑(MDZ)是 NICU 中常用的新生儿镇静剂,有研究表明它会增加儿童学习障碍和认知障碍。然而,在生命早期长期使用 MDZ 导致这种结果的分子机制尚不清楚。在这项研究中,我们首次阐明了脑源性细胞外囊泡(BDEVs)的作用,包括在早期发育过程中,对长期 MDZ 暴露后 BDEV 蛋白质组进行挖掘。我们使用先前建立的啮齿动物模型系统,该系统通过递增剂量方案模拟 NICU 中 MDZ 的暴露,从出生后 21 天的对照组和 MDZ 组中分离 BDEVs。然后使用 ZetaView 纳米颗粒跟踪分析仪和透射电子显微镜分析对来自对照组和 MDZ 组的 BDEVs 进行表征。接下来,我们使用 RT-qPCR 检查了参与 EV 生物发生的关键 ESCRT 相关基因的表达。最后,使用基于定量质谱的蛋白质组学,我们挖掘了 BDEV 蛋白货物,揭示了关键差异表达蛋白及其相关分子途径在长期 MDZ 暴露后发生改变。我们的研究在早期发育过程中对长期 MDZ 暴露的 BDEV 货物的蛋白质组进行了特征描述。重要的是,我们鉴定并验证了 YWHAH 的表达,作为其下游机制的进一步特征描述和神经发育和神经退行性疾病早期发病的潜在生物标志物。总的来说,本研究表明,早期发育阶段长期暴露于 MDZ 可能会影响 BDEV 蛋白质货物,从而可能影响后期发育阶段的神经功能和行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f45/10047367/ac0e9acda1e1/cells-12-00966-g001.jpg

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