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暴露于城市颗粒物的小鼠海马体和皮层中的神经退行性途径和代谢变化:来自综合互作网络分析的见解。

Neurodegenerative pathways and metabolic changes in the hippocampus and cortex of mice exposed to urban particulate matter: Insights from an integrated interactome analysis.

机构信息

KM Convergence Research Division, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon 34054, Republic of Korea.

KM Convergence Research Division, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon 34054, Republic of Korea.

出版信息

Sci Total Environ. 2024 Oct 1;945:173673. doi: 10.1016/j.scitotenv.2024.173673. Epub 2024 Jun 4.

Abstract

Recently, urban particulate matter (UPM) exposure has been associated with the development of brain disorders. This study uses bioinformatic analyses to elucidate the molecular unexplored mechanisms underlying the effects of UPM exposure on the brain. Mice are exposed to UPM (from 3 days to 20 weeks), and their behavioral patterns measured. We measure pathology and gene expression in the hippocampus and cortical regions of the brain. An integrated interactome of genes is established, which enriches information on metabolic processes. Using this network, we isolate the core genes that are differentially expressed in the samples. We observe cognitive loss and pathological changes in the brains of mice at 16 or 20 weeks of exposure. Through network analysis of core-differential genes and measurement of pathway activity, we identify differences in the response to UPM exposure between the hippocampus and cortex. However, neurodegenerative disease pathways are implicated in both tissues following short-term exposure to UPM. There were also significant changes in metabolic function in both tissues depending on UPM exposure time. Additionally, the cortex of UPM-exposed mice shows more similarities with psychiatric disorders than with neurodegenerative diseases. The connectivity map database is used to isolate genes contributing to changes in expression due to UPM exposure. New approaches for inhibiting or preventing the brain damage caused by UPM exposure can be developed by targeting the functions and selected genes identified in this study.

摘要

最近,城市颗粒物(UPM)暴露与脑部疾病的发展有关。本研究使用生物信息学分析来阐明 UPM 暴露对大脑影响的分子机制。将小鼠暴露于 UPM(3 天至 20 周),并测量其行为模式。我们测量了海马体和大脑皮质区域的病理学和基因表达。建立了一个综合的基因互作网络,丰富了代谢过程的信息。利用这个网络,我们分离出在样本中差异表达的核心基因。我们观察到在暴露 16 或 20 周后,小鼠的认知能力下降和大脑出现病理变化。通过对核心差异基因的网络分析和途径活性的测量,我们确定了 UPM 暴露在海马体和皮质中的反应差异。然而,在 UPM 短期暴露后,两种组织中的神经退行性疾病途径都涉及其中。两种组织的代谢功能也因 UPM 暴露时间的不同而发生显著变化。此外,暴露于 UPM 的小鼠的皮质与精神疾病的相似性高于与神经退行性疾病的相似性。使用连接图谱数据库分离由于 UPM 暴露导致表达变化的基因。通过针对本研究中确定的功能和选定的基因,开发出抑制或预防 UPM 暴露引起的大脑损伤的新方法。

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