
doi: 10.1002/cne.25212
pmid: 34235750
Abstract The axon initial segment (AIS) is structurally and functionally distinct from other regions of the axon, yet alterations in the milieu of the AIS after brain injury have not been well characterized. In this study, we have examined extracellular and intracellular changes in the AIS after hypoglossal nerve injury. Microglial adhesions to the AIS were rarely observed in healthy controls, whereas microglial adhesions to the AIS became apparent in the axonal injury model. Regarding intra‐AIS morphology, we focused on mitochondria because mitochondrial flow into the injured axon appears critical for axonal regeneration. To visualize mitochondria specifically in injured axons, we used Atf3 :BAC transgenic mice whose mitochondria were labeled with GFP in response to nerve injury. These mice clearly showed mitochondrial localization in the AIS after nerve injury. To precisely confirm the light microscopic observations, we performed three‐dimensional ultrastructural analysis using focused ion beam/scanning electron microscopy (FIB/SEM). Although the healthy AIS was not surrounded by microglia, tight microglial adhesions with thick processes adhering to the AIS were observed after injury. FIB/SEM simultaneously allowed the observation of mitochondrial localization in the AIS. In the AIS of non‐injured neurons, few mitochondria were observed, whereas mitochondria were abundantly localized in the cell body, axon hillock, and axon. Intriguingly, in the injured AIS, numerous mitochondria were observed throughout the AIS. Taken together, axonal injury changes the extracellular glial environment surrounding the AIS and intracellular mitochondrial localization in the AIS. These changes would be crucial responses, perhaps for injured neurons to regenerate after axonal injury.
Male, Activating Transcription Factor 3, Nerve Crush, Mice, Transgenic, Immunohistochemistry, Axons, Mitochondria, Mice, Inbred C57BL, Mice, Imaging, Three-Dimensional, Cell Adhesion, Animals, Humans, Female, Extracellular Space, Neuroglia, Axon Initial Segment
Male, Activating Transcription Factor 3, Nerve Crush, Mice, Transgenic, Immunohistochemistry, Axons, Mitochondria, Mice, Inbred C57BL, Mice, Imaging, Three-Dimensional, Cell Adhesion, Animals, Humans, Female, Extracellular Space, Neuroglia, Axon Initial Segment
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