摘要：SummaryThe axon initial segment (AIS) cytoskeleton undergoes rapid and irreversible disruption prior to cell death after injury, and loss of AIS integrity can produce profound neurological effects on the nervous system. Here we described a previously unrecognized mechanism for ischemia-induced alterations in AIS integrity. We show that in hippocampal CA1 pyramidal neurons Nav1.6 mostly preserves at the AIS after disruption of the cytoskeleton in a mouse model of middle cerebral artery occlusion. Genetic removal of neurofascin-186 leads to rapid disruption of Nav1.6 following injury, indicating that neurofascin is required for Nav1.6 maintenance at the AIS after cytoskeleton collapse. Importantly, calcineurin inhibition with FK506 fully protects AIS integrity and sufficiently prevents impairments of spatial learning and memory from injury. This study provides evidence that calcineurin activation is primarily involved in initiating disassembly of the AIS cytoskeleton and that maintaining AIS integrity is crucial for therapeutic strategies to facilitate recovery from injury.Graphical AbstractDisplay OmittedHighlights•Ion channels are mostly retained at the AIS after ischemic injury•Neurofascin is required for clustering ion channels at the AIS after ischemia•Calcineurin inhibition protects AIS structural integrity and function from ischemia•Calcineurin inhibition protects cognitive function against impairment by ischemiaNeuroscience; Molecular Neuroscience; Cellular Neuroscience
