Department of Cell and Developmental Biology, University of Colorado School of Medicine, United States.
Department of Cell and Developmental Biology, University of Colorado School of Medicine, United States.
Neurosci Lett. 2020 May 14;727:134916. doi: 10.1016/j.neulet.2020.134916. Epub 2020 Mar 16.
Oligodendrocyte lineage cells (oligodendroglia) and neurons engage in bidirectional communication throughout life to support healthy brain function. Recent work shows that changes in neuronal activity can modulate proliferation, differentiation, and myelination to support the formation and function of neural circuits. While oligodendroglia express a diverse collection of receptors for growth factors, signaling molecules, neurotransmitters and neuromodulators, our knowledge of the intracellular signaling pathways that are regulated by neuronal activity remains largely incomplete. Many of the pathways that modulate oligodendroglia behavior are driven by changes in intracellular calcium signaling, which may differentially affect cytoskeletal dynamics, gene expression, maturation, integration, and axonal support. Additionally, activity-dependent neuron-oligodendroglia communication plays an integral role in the recovery from demyelinating injuries. In this review, we summarize the modalities of communication between neurons and oligodendroglia and explore possible roles of activity-dependent calcium signaling in mediating cellular behavior and myelination.
少突胶质细胞谱系细胞(少突胶质细胞)和神经元在整个生命过程中进行双向通讯,以支持大脑的健康功能。最近的研究表明,神经元活动的变化可以调节增殖、分化和髓鞘形成,以支持神经回路的形成和功能。虽然少突胶质细胞表达了大量的生长因子、信号分子、神经递质和神经调质的受体,但我们对受神经元活动调节的细胞内信号通路的了解仍在很大程度上不完整。许多调节少突胶质细胞行为的途径是由细胞内钙信号的变化驱动的,这可能会对细胞骨架动力学、基因表达、成熟、整合和轴突支持产生不同的影响。此外,活性依赖性神经元-少突胶质细胞通讯在脱髓鞘损伤的恢复中起着至关重要的作用。在这篇综述中,我们总结了神经元和少突胶质细胞之间的通讯方式,并探讨了活性依赖性钙信号在调节细胞行为和髓鞘形成中的可能作用。