酒精诱导少突胶质细胞浓度依赖性转录组变化

IF 2.6 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Addiction Biology Pub Date : 2025-02-12 DOI:10.1111/adb.70012
Sam A. Bazzi, Cole Maguire, R. Dayne Mayfield, Esther Melamed
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摘要

少突胶质细胞是中枢神经系统(CNS)中的一种关键细胞类型,它产生覆盖轴突的髓鞘,使神经元信号能够快速传播。已知饮酒会影响中枢神经系统的少突胶质细胞和白质。然而,大多数研究都集中在胎儿酒精谱系障碍和严重酒精使用障碍上。此外,酒精剂量对少突胶质细胞的影响以前没有研究过。在这项研究中,我们评估了暴露于中高浓度酒精后C57BL6/J培养的成熟少突胶质细胞的转录组学变化。我们发现高浓度酒精会引发多种生物途径的基因表达变化,包括髓鞘形成、蛋白质翻译、整合素信号传导、细胞周期调节和炎症。此外,我们的研究结果表明,转录组的变化确实依赖于酒精浓度,中度和高浓度的酒精会引发不同的基因表达谱。总之,我们的研究表明,酒精诱导的少突胶质细胞转录组变化是浓度依赖性的,可能对髓磷脂的产生有关键的下游影响。以酒精诱导的细胞周期调节、整合素信号、炎症或蛋白质翻译调节的变化为目标,可能揭示髓磷脂产生或抑制的调节机制。此外,更深入地了解酒精对少突胶质细胞脱髓鞘和髓鞘再生的影响,可能有助于发现可独立于酒精的治疗途径,以帮助髓鞘再生药物设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Alcohol induces concentration-dependent transcriptomic changes in oligodendrocytes

Oligodendrocytes are a key cell type within the central nervous system (CNS) that generates the myelin sheath covering axons, enabling fast propagation of neuronal signals. Alcohol consumption is known to affect oligodendrocytes and white matter in the CNS. However, most studies have focused on foetal alcohol spectrum disorder and severe alcohol use disorder. Additionally, the impact of alcohol dosage on oligodendrocytes has not been previously investigated. In this study, we evaluated transcriptomic changes in C57BL6/J cultured mature oligodendrocytes following exposure to moderate and high concentrations of alcohol. We found that high concentrations of alcohol elicited gene expression changes across a wide range of biological pathways, including myelination, protein translation, integrin signalling, cell cycle regulation and inflammation. Further, our results demonstrate that transcriptomic changes are indeed dependent on alcohol concentration, with moderate and high concentrations of alcohol provoking distinct gene expression profiles. In conclusion, our study demonstrates that alcohol-induced transcriptomic changes in oligodendrocytes are concentration-dependent and may have critical downstream impacts on myelin production. Targeting alcohol-induced changes in cell cycle regulation, integrin signalling, inflammation or protein translation regulation may uncover mechanisms for modulating myelin production or inhibition. Furthermore, gaining a deeper understanding of alcohol's effects on oligodendrocyte demyelination and remyelination could help uncover therapeutic pathways that can be utilized independently of alcohol to aid in remyelinating drug design.

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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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