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髓鞘轴突的生理学和病理学中的线粒体动态。

Mitochondrial Dynamics in Physiology and Pathology of Myelinated Axons.

机构信息

Division of Neurobiology and Bioinformatics, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.

Departments of Anatomy and Structural Biology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo, Yamanashi, Japan.

出版信息

Adv Exp Med Biol. 2019;1190:145-163. doi: 10.1007/978-981-32-9636-7_10.

Abstract

Mitochondria play essential roles in neurons and abnormal functions of mitochondria have been implicated in neurological disorders including myelin diseases. Since mitochondrial functions are regulated and maintained by their dynamic behavior involving localization, transport, and fusion/fission, modulation of mitochondrial dynamics would be involved in physiology and pathology of myelinated axons. In fact, the integration of multimodal imaging in vivo and in vitro revealed that mitochondrial localization and transport are differentially regulated in nodal and internodal regions in response to the changes of metabolic demand in myelinated axons. In addition, the mitochondrial behavior in axons is modulated as adaptive responses to demyelination irrespective of the cause of myelin loss, and the behavioral modulation is partly through interactions with cytoskeletons and closely associated with the pathophysiology of demyelinating diseases. Furthermore, the behavior and functions of axonal mitochondria are modulated in congenital myelin disorders involving impaired interactions between axons and myelin-forming cells, and, together with the inflammatory environment, implicated in axonal degeneration and disease phenotypes. Further studies on the regulatory mechanisms of the mitochondrial dynamics in myelinated axons would provide deeper insights into axo-glial interactions mediated through myelin ensheathment, and effective manipulations of the dynamics may lead to novel therapeutic strategies protecting axonal and neuronal functions and survival in primary diseases of myelin.

摘要

线粒体在神经元中发挥着重要作用,线粒体功能异常与包括髓鞘疾病在内的神经紊乱有关。由于线粒体的功能是通过其涉及定位、运输和融合/分裂的动态行为来调节和维持的,因此线粒体动力学的调节将涉及有髓轴突的生理学和病理学。事实上,体内和体外多模态成像的整合表明,线粒体在节点和节间区的定位和运输是不同的,以响应有髓轴突代谢需求的变化。此外,线粒体在轴突中的行为被调节为适应脱髓鞘的反应,而不论髓磷脂丧失的原因如何,并且行为调节部分是通过与细胞骨架的相互作用,并与脱髓鞘疾病的病理生理学密切相关。此外,涉及轴突和髓鞘形成细胞之间相互作用受损的先天性髓鞘疾病中的轴突线粒体的行为和功能也受到调节,并且与炎症环境一起,与轴突变性和疾病表型有关。进一步研究髓鞘轴突中线粒体动力学的调节机制将深入了解通过髓鞘包绕介导的轴突-胶质相互作用,并且对动力学的有效操纵可能导致保护轴突和神经元功能和存活的新型治疗策略,这些策略针对髓鞘的原发性疾病。

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