Moura Daniela M S, Brennan Emma J, Brock Robert, Cocas Laura A
Department of Biology, Santa Clara University, Santa Clara, CA, United States.
Department of Neurology, University of California, San Francisco, San Francisco, CA, United States.
Front Neurosci. 2022 Jan 18;15:779125. doi: 10.3389/fnins.2021.779125. eCollection 2021.
The development of neuronal circuitry required for cognition, complex motor behaviors, and sensory integration requires myelination. The role of glial cells such as astrocytes and microglia in shaping synapses and circuits have been covered in other reviews in this journal and elsewhere. This review summarizes the role of another glial cell type, oligodendrocytes, in shaping synapse formation, neuronal circuit development, and myelination in both normal development and in demyelinating disease. Oligodendrocytes ensheath and insulate neuronal axons with myelin, and this facilitates fast conduction of electrical nerve impulses via saltatory conduction. Oligodendrocytes also proliferate during postnatal development, and defects in their maturation have been linked to abnormal myelination. Myelination also regulates the timing of activity in neural circuits and is important for maintaining the health of axons and providing nutritional support. Recent studies have shown that dysfunction in oligodendrocyte development and in myelination can contribute to defects in neuronal synapse formation and circuit development. We discuss glutamatergic and GABAergic receptors and voltage gated ion channel expression and function in oligodendrocyte development and myelination. We explain the role of excitatory and inhibitory neurotransmission on oligodendrocyte proliferation, migration, differentiation, and myelination. We then focus on how our understanding of the synaptic connectivity between neurons and OPCs can inform future therapeutics in demyelinating disease, and discuss gaps in the literature that would inform new therapies for remyelination.
认知、复杂运动行为和感觉整合所需的神经回路发育需要髓鞘形成。星形胶质细胞和小胶质细胞等胶质细胞在塑造突触和神经回路方面的作用已在本期刊及其他地方的其他综述中有所涵盖。本综述总结了另一种胶质细胞类型——少突胶质细胞在正常发育和脱髓鞘疾病中塑造突触形成、神经回路发育和髓鞘形成方面的作用。少突胶质细胞用髓鞘包裹并绝缘神经元轴突,这通过跳跃传导促进神经电冲动的快速传导。少突胶质细胞在出生后发育过程中也会增殖,其成熟缺陷与髓鞘形成异常有关。髓鞘形成还调节神经回路中活动的时间,对维持轴突健康和提供营养支持很重要。最近的研究表明,少突胶质细胞发育和髓鞘形成功能障碍可导致神经元突触形成和神经回路发育缺陷。我们讨论了谷氨酸能和γ-氨基丁酸能受体以及电压门控离子通道在少突胶质细胞发育和髓鞘形成中的表达和功能。我们解释了兴奋性和抑制性神经传递对少突胶质细胞增殖、迁移、分化和髓鞘形成的作用。然后,我们重点关注我们对神经元与少突胶质前体细胞之间突触连接的理解如何为脱髓鞘疾病的未来治疗提供信息,并讨论文献中的空白,这些空白将为髓鞘再生的新疗法提供信息。