NeuroD2在衰老过程中调节海马神经元组织和轴突引导。

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-07-01 DOI:10.21873/invivo.14000
Merve Beker, Busenur Bolat, Bahar Sarikamis Johnson, Nilufer Ercin, Rabia Kalkan Cakmak, Sare B Kaya, Nail Besli, Ulkan Celik, Mustafa C Beker
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引用次数: 0

摘要

背景/目的:生物老化是指由于细胞和分子损伤的累积而导致机体功能的逐渐退化。NeuroD2是一种重要的转录因子,在神经元发育和突触成熟中起着至关重要的作用。本研究探讨了NeuroD2在海马神经元组织中的作用,重点研究了衰老过程中的门门苔藓细胞,并利用生物信息学方法鉴定了与细胞衰老相关的NeuroD2靶点。材料和方法:选用成年C57Bl/6小鼠21只,分为幼年(2个月)、老年(12个月)和老年(24个月)三个年龄组。小鼠在安乐死前10天,连续3天腹腔注射BrdU。采集脑组织,利用免疫荧光、Western blotting和实时荧光定量PCR分析海马组织中NeuroD2的表达和相关信号通路。此外,生物信息学分析使用两个开放获取数据集(ProteomeXchange Consortium,数据集标识符:PXD043352;Gene Expression Omnibus, GEO: GSE67539),并探索NeuroD2靶点与生物衰老成分之间的潜在相互作用。结果:我们的研究结果显示,随着年龄的增长,NeuroD2的表达发生了显著变化,并与AKT信号通路相关。此外,我们发现了NeuroD2活性与AKT通路之间的潜在联系,表明NeuroD2在减轻衰老相关应激中的作用。生物信息学分析鉴定出513个下调蛋白和638个上调蛋白,其中涉及轴突投射的NeuroD2靶点在老年小鼠中表达增加。与预期相反,途径富集分析突出了轴突引导分子而不是氧化应激标记物。结论:本研究强调了NeuroD2在保持海马完整性中的关键作用,并揭示了与年龄相关的神经元变化的分子机制。我们的研究结果揭示了NeuroD2在健康衰老过程中调节关键通路的作用,并有可能减轻衰老的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NeuroD2 Modulates Hippocampal Neuronal Organization and Axon Guidance During Aging.

Background/aim: Biological aging refers to the progressive deterioration of an organism's functions due to accumulated cellular and molecular damage. NeuroD2, a critical transcription factor, plays a crucial role in neuronal development and synaptic maturation. This study investigates the role of NeuroD2 in hippocampal neuron organization, focusing on hilar mossy cells during aging, and employs bioinformatics to identify NeuroD2 targets linked to cellular aging.

Materials and methods: We used 21 adult C57Bl/6 mice, categorized into three age groups: young (2 months), old (12 months), and very old (24 months). Mice were administered BrdU intraperitoneally for three consecutive days, 10 days before euthanasia. The brains were harvested and analyzed using immunofluorescence, Western blotting, and quantitative real-time PCR to evaluate NeuroD2 expression and associated signaling pathways in hippocampal tissue. Additionally, bioinformatics analysis was performed using two open-access datasets (ProteomeXchange Consortium, Dataset identifier: PXD043352; Gene Expression Omnibus, GEO: GSE67539) and to explore potential interactions between NeuroD2 targets and biological aging components.

Results: Our results revealed that NeuroD2 expression changed significantly with age and correlated with AKT signaling. Moreover, we identified a potential link between NeuroD2 activity and the AKT pathway, indicating NeuroD2's role in mitigating aging-related stress. Bioinformatics analysis identified 513 down-regulated and 638 up-regulated proteins, with NeuroD2 targets involved in axonal projection showing increased expression in older mice. Contrary to expectations, pathway enrichment analysis highlighted axon guidance molecules rather than oxidative stress markers.

Conclusion: This study underscores NeuroD2's critical role in preserving hippocampal integrity and reveals molecular mechanisms underlying age-related neuronal changes. Our findings provide insights into the role of NeuroD2 in regulating key pathways during healthy aging, potentially mitigating the impacts of aging.

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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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