成年小鼠少突胶质细胞的消减会改变大脑的微观结构和活动,而与行为缺陷无关。

IF 5.4 2区 医学 Q1 NEUROSCIENCES Glia Pub Date : 2024-07-09 DOI:10.1002/glia.24576
Malte S. Kaller, Alberto Lazari, Yingshi Feng, Annette van der Toorn, Sebastian Rühling, Christopher W. Thomas, Takahiro Shimizu, David Bannerman, Vladyslav Vyazovskiy, William D. Richardson, Cassandra Sampaio-Baptista, Heidi Johansen-Berg
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引用次数: 0

摘要

少突胶质细胞在成年后仍会继续从其前体细胞分化,这一过程可受神经元活动和经验的调节。以前的研究表明,有条件地消减成年小鼠的少突胶质细胞分化,会导致小鼠在一系列行为任务中出现学习和记忆障碍。目前的研究利用复杂的跑轮任务,复制并重新评估了少突胶质细胞在运动学习中发挥作用的证据。此外,我们还发现,消融少突胶质细胞会改变大脑微结构(体外核磁共振成像)和大脑活动(体内脑电图),与任务经验无关。这表明成年少突胶质细胞的形成在维持大脑功能中的作用,并表明在解释该模型中的学习和记忆缺陷时,需要考虑少突胶质细胞消减引起的与任务无关的变化。
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Ablation of oligodendrogenesis in adult mice alters brain microstructure and activity independently of behavioral deficits

Oligodendrocytes continue to differentiate from their precursor cells even in adulthood, a process that can be modulated by neuronal activity and experience. Previous work has indicated that conditional ablation of oligodendrogenesis in adult mice leads to learning and memory deficits in a range of behavioral tasks. The current study replicated and re-evaluated evidence for a role of oligodendrogenesis in motor learning, using a complex running wheel task. Further, we found that ablating oligodendrogenesis alters brain microstructure (ex vivo MRI) and brain activity (in vivo EEG) independent of experience with the task. This suggests a role for adult oligodendrocyte formation in the maintenance of brain function and indicates that task-independent changes due to oligodendrogenesis ablation need to be considered when interpreting learning and memory deficits in this model.

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来源期刊
Glia
Glia 医学-神经科学
CiteScore
13.10
自引率
4.80%
发文量
162
审稿时长
3-8 weeks
期刊介绍: GLIA is a peer-reviewed journal, which publishes articles dealing with all aspects of glial structure and function. This includes all aspects of glial cell biology in health and disease.
期刊最新文献
All the single cells: Single-cell transcriptomics/epigenomics experimental design and analysis considerations for glial biologists. R-Ras1 and R-Ras2 regulate mature oligodendrocyte subpopulations. Astrocytic NHERF-1 Increases Seizure Susceptibility by Inhibiting Surface Expression of TREK-1. Aquaporin-4 activation facilitates glymphatic system function and hematoma clearance post-intracerebral hemorrhage. The E3 ubiquitin ligase Nedd4 fosters developmental myelination in the mouse central and peripheral nervous system.
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