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      A HIERARCHY OF ANKYRIN/SPECTRIN COMPLEXES CLUSTERS SODIUM CHANNELS AT NODES OF RANVIER

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          SUMMARY

          The scaffolding protein ankyrinG is required for Na+ channel clustering at axon initial segments. It is also considered essential for Na+ channel clustering at nodes of Ranvier to facilitate fast and efficient action potential propagation. However, in contrast to these widely accepted roles, we show here that ankyrinG is dispensable for nodal Na+ channel clustering in vivo. Surprisingly, without ankyrinG, erythrocyte ankyrin (ankyrinR) and its binding partner βI spectrin substitute and rescue nodal Na+ channel clustering. In addition, channel clustering is also rescued after loss of nodal βIV spectrin by βI spectrin and ankyrinR. In mice lacking both ankyrinG and ankyrinR, Na+ channels fail to cluster at nodes. Thus, ankyrinR/βI spectrin protein complexes function as secondary reserve Na+ channel clustering machinery, and two independent ankyrin/spectrin protein complexes exist in myelinated axons to cluster Na+ channels at nodes of Ranvier.

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          Most cited references44

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          AnkyrinG Is Required for Clustering of Voltage-gated Na Channels at Axon Initial Segments and for Normal Action Potential Firing

          Voltage-gated sodium channels (NaCh) are colocalized with isoforms of the membrane-skeletal protein ankyrinG at axon initial segments, nodes of Ranvier, and postsynaptic folds of the mammalian neuromuscular junction. The role of ankyrinG in directing NaCh localization to axon initial segments was evaluated by region-specific knockout of ankyrinG in the mouse cerebellum. Mutant mice exhibited a progressive ataxia beginning around postnatal day P16 and subsequent loss of Purkinje neurons. In mutant mouse cerebella, NaCh were absent from axon initial segments of granule cell neurons, and Purkinje cells showed deficiencies in their ability to initiate action potentials and support rapid, repetitive firing. Neurofascin, a member of the L1CAM family of ankyrin-binding cell adhesion molecules, also exhibited impaired localization to initial segments of Purkinje cell neurons. These results demonstrate that ankyrinG is essential for clustering NaCh and neurofascin at axon initial segments and is required for physiological levels of sodium channel activity.
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            A distal axonal cytoskeleton forms an intra-axonal boundary that controls axon initial segment assembly.

            AnkyrinG (ankG) is highly enriched in neurons at axon initial segments (AISs) where it clusters Na(+) and K(+) channels and maintains neuronal polarity. How ankG becomes concentrated at the AIS is unknown. Here, we show that as neurons break symmetry, they assemble a distal axonal submembranous cytoskeleton, comprised of ankyrinB (ankB), αII-spectrin, and βII-spectrin, that defines a boundary limiting ankG to the proximal axon. Experimentally moving this boundary altered the length of ankG staining in the proximal axon, whereas disruption of the boundary through silencing of ankB, αII-spectrin, or βII-spectrin expression blocked AIS assembly and permitted ankG to redistribute throughout the distal axon. In support of an essential role for the distal cytoskeleton in ankG clustering, we also found that αII and βII-spectrin-deficient mice had disrupted AIS. Thus, the distal axonal cytoskeleton functions as an intra-axonal boundary restricting ankG to the AIS. Copyright © 2012 Elsevier Inc. All rights reserved.
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              Neurofascins are required to establish axonal domains for saltatory conduction.

              Voltage-gated sodium channels are concentrated in myelinated nerves at the nodes of Ranvier flanked by paranodal axoglial junctions. Establishment of these essential nodal and paranodal domains is determined by myelin-forming glia, but the mechanisms are not clear. Here, we show that two isoforms of Neurofascin, Nfasc155 in glia and Nfasc186 in neurons, are required for the assembly of these specialized domains. In Neurofascin-null mice, neither paranodal adhesion junctions nor nodal complexes are formed. Transgenic expression of Nfasc155 in the myelinating glia of Nfasc-/- nerves rescues the axoglial adhesion complex by recruiting the axonal proteins Caspr and Contactin to the paranodes. However, in the absence of Nfasc186, sodium channels remain diffusely distributed along the axon. Our study shows that the two major Neurofascins play essential roles in assembling the nodal and paranodal domains of myelinated axons; therefore, they are essential for the transition to saltatory conduction in developing vertebrate nerves.
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                Author and article information

                Journal
                9809671
                21092
                Nat Neurosci
                Nat. Neurosci.
                Nature neuroscience
                1097-6256
                1546-1726
                10 October 2014
                02 November 2014
                December 2014
                01 June 2015
                : 17
                : 12
                : 1664-1672
                Affiliations
                [1 ]Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030
                [2 ]Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030
                [3 ]Department of Neurology, Baylor College of Medicine, Houston, TX 77030
                [4 ]Department of Pathology, Yale University, New Haven, CT 06520
                [5 ]Department of Cell Biology, Duke University, Durham, NC 27710
                Author notes
                [* ]Correspondence should be addressed to: Dr. Matthew N. Rasband, Department of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, Tel: 713-798-4494, Fax: 713-798-3946, rasband@ 123456bcm.edu
                Article
                NIHMS634421
                10.1038/nn.3859
                4271271
                25362473
                d338eeb8-3809-4b40-bf80-87a78493ba16
                History
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                Neurosciences
                Neurosciences

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