将分子方法转化为少突胶质细胞介导的神经回路调节

Translating Molecular Approaches to Oligodendrocyte-Mediated Neurological Circuit Modulation.

作者信息

Song Jingwei, Saglam Aybike, Zuchero J Bradley, Buch Vivek P

机构信息

Medical Scientist Training Program, School of Medicine, Stanford University, Stanford, CA 94305, USA.

Department of Neurosurgery, Stanford University, Stanford, CA 94305, USA.

出版信息

Brain Sci. 2024 Jun 27;14(7):648. doi: 10.3390/brainsci14070648.

Abstract

The central nervous system (CNS) exhibits remarkable adaptability throughout life, enabled by intricate interactions between neurons and glial cells, in particular, oligodendrocytes (OLs) and oligodendrocyte precursor cells (OPCs). This adaptability is pivotal for learning and memory, with OLs and OPCs playing a crucial role in neural circuit development, synaptic modulation, and myelination dynamics. Myelination by OLs not only supports axonal conduction but also undergoes adaptive modifications in response to neuronal activity, which is vital for cognitive processing and memory functions. This review discusses how these cellular interactions and myelin dynamics are implicated in various neurocircuit diseases and disorders such as epilepsy, gliomas, and psychiatric conditions, focusing on how maladaptive changes contribute to disease pathology and influence clinical outcomes. It also covers the potential for new diagnostics and therapeutic approaches, including pharmacological strategies and emerging biomarkers in oligodendrocyte functions and myelination processes. The evidence supports a fundamental role for myelin plasticity and oligodendrocyte functionality in synchronizing neural activity and high-level cognitive functions, offering promising avenues for targeted interventions in CNS disorders.

摘要

中枢神经系统(CNS)在整个生命过程中表现出显著的适应性,这得益于神经元与神经胶质细胞之间复杂的相互作用,特别是少突胶质细胞(OLs)和少突胶质细胞前体细胞(OPCs)。这种适应性对于学习和记忆至关重要,OLs和OPCs在神经回路发育、突触调节和髓鞘形成动力学中发挥着关键作用。OLs形成的髓鞘不仅支持轴突传导,还会根据神经元活动进行适应性改变,这对认知加工和记忆功能至关重要。本综述讨论了这些细胞间相互作用和髓鞘动力学如何与各种神经回路疾病和障碍(如癫痫、神经胶质瘤和精神疾病)相关,重点关注适应不良的变化如何导致疾病病理并影响临床结果。它还涵盖了新的诊断和治疗方法的潜力,包括药理学策略以及少突胶质细胞功能和髓鞘形成过程中新兴的生物标志物。证据支持髓鞘可塑性和少突胶质细胞功能在同步神经活动和高级认知功能方面的基本作用,为中枢神经系统疾病的靶向干预提供了有希望的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f40/11275066/1e4e337e7dad/brainsci-14-00648-g001.jpg

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