Formation and disruption of functional domains in myelinated CNS axons

• Published in: Neuroscience research Vol. 116; pp. 77 - 87
• Main Authors: Griggs, Ryan B., Yermakov, Leonid M., Susuki, Keiichiro
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 01.03.2017
• Subjects: Action Potentials; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Animals; Axon initial segment; Axons - physiology; Brain Injuries - metabolism; Brain Injuries - pathology; Calpain; Calpain - metabolism; Central Nervous System - metabolism; Humans; Mitochondria; Mitochondria - metabolism; Multiple Sclerosis - metabolism; Multiple Sclerosis - pathology; Myelin Sheath - physiology; Neurological disease; Node of Ranvier; Ranvier's Nodes - physiology; Node of Ranvier; Calpain; Mitochondria; Neurological disease; Axon initial segment
• ISSN: 0168-0102; 1872-8111
• DOI: 10.1016/j.neures.2016.09.010

•Intrinsic axonal mechanisms regulate axon initial segment formation.•Myelination regulates node of Ranvier formation and mitochondrial distribution.•Calpains target molecular complexes at the axon initial segment and nodes.•Mitochondrial perturbation contributes to demyelinating diseases.•Disruption of excitable domains is a common mechanism of neurological diseases. Communication in the central nervous system (CNS) occurs through initiation and propagation of action potentials at excitable domains along axons. Action potentials generated at the axon initial segment (AIS) are regenerated at nodes of Ranvier through the process of saltatory conduction. Proper formation and maintenance of the molecular structure at the AIS and nodes are required for sustaining conduction fidelity. In myelinated CNS axons, paranodal junctions between the axolemma and myelinating oligodendrocytes delineate nodes of Ranvier and regulate the distribution and localization of specialized functional elements, such as voltage-gated sodium channels and mitochondria. Disruption of excitable domains and altered distribution of functional elements in CNS axons is associated with demyelinating diseases such as multiple sclerosis, and is likely a mechanism common to other neurological disorders. This review will provide a brief overview of the molecular structure of the AIS and nodes of Ranvier, as well as the distribution of mitochondria in myelinated axons. In addition, this review highlights important structural and functional changes within myelinated CNS axons that are associated with neurological dysfunction.