少突胶质细胞谱系中的钙信号传导:调节因子和后果。

IF 12.1 1区 医学 Q1 NEUROSCIENCES Annual review of neuroscience Pub Date : 2020-07-08 Epub Date: 2020-02-19 DOI:10.1146/annurev-neuro-100719-093305
Pablo M Paez, David A Lyons
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引用次数: 36

摘要

少突胶质细胞谱系的细胞表达广泛的Ca2+通道和受体,调节少突胶质细胞祖细胞(OPC)和少突胶质细胞的形成和功能。在这里,我们定义了调节Ca2+信号和OPC发育和髓鞘形成的关键通道和受体。然后,我们讨论细胞内Ca2+的调节如何反过来影响OPC和少突胶质细胞生物学在健康的神经系统和病理条件下。神经递质激活OPCs和少突胶质细胞中的Ca2+通道和受体,集中于调节细胞内Ca2+,使Ca2+信号成为活性驱动髓鞘形成的中心候选介质。事实上,最近的证据表明,Ca2+在少突胶质细胞中的局部变化可以调节髓鞘的形成和重塑,并可能调节少突胶质细胞和OPCs的其他功能。因此,解码OPCs和髓鞘少突胶质细胞如何整合和处理Ca2+信号对于充分了解中枢神经系统的形成、健康和功能将是重要的。
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Calcium Signaling in the Oligodendrocyte Lineage: Regulators and Consequences.

Cells of the oligodendrocyte lineage express a wide range of Ca2+ channels and receptors that regulate oligodendrocyte progenitor cell (OPC) and oligodendrocyte formation and function. Here we define those key channels and receptors that regulate Ca2+ signaling and OPC development and myelination. We then discuss how the regulation of intracellular Ca2+ in turn affects OPC and oligodendrocyte biology in the healthy nervous system and under pathological conditions. Activation of Ca2+ channels and receptors in OPCs and oligodendrocytes by neurotransmitters converges on regulating intracellular Ca2+, making Ca2+ signaling a central candidate mediator of activity-driven myelination. Indeed, recent evidence indicates that localized changes in Ca2+ in oligodendrocytes can regulate the formation and remodeling of myelin sheaths and perhaps additional functions of oligodendrocytes and OPCs. Thus, decoding how OPCs and myelinating oligodendrocytes integrate and process Ca2+ signals will be important to fully understand central nervous system formation, health, and function.

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来源期刊
Annual review of neuroscience
Annual review of neuroscience 医学-神经科学
CiteScore
25.30
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Neuroscience is a well-established and comprehensive journal in the field of neuroscience, with a rich history and a commitment to open access and scholarly communication. The journal has been in publication since 1978, providing a long-standing source of authoritative reviews in neuroscience. The Annual Review of Neuroscience encompasses a wide range of topics within neuroscience, including but not limited to: Molecular and cellular neuroscience, Neurogenetics, Developmental neuroscience, Neural plasticity and repair, Systems neuroscience, Cognitive neuroscience, Behavioral neuroscience, Neurobiology of disease. Occasionally, the journal also features reviews on the history of neuroscience and ethical considerations within the field.
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