Literature DB >> 30784979

Subcellular control of membrane excitability in the axon.

Scott A Alpizar1, In Ha Cho1, Michael B Hoppa2.   

Abstract

Ion channels are microscopic pore proteins in the membrane that open and close in response to chemical and electrical stimuli. This simple concept underlies rapid electrical signaling in the brain as well as several important aspects of neural plasticity. Although the soma accounts for less than 1% of many neurons by membrane area, it has been the major site of measuring ion channel function. However, the axon is one of the longest processes found in cellular biology and hosts a multitude of critical signaling functions in the brain. Not only does the axon initiate and rapidly propagate action potentials (APs) across the brain but it also forms the presynaptic terminals that convert these electrical inputs into chemical outputs. Here, we review recent advances in the physiological role of ion channels within the diverse landscape of the axon and presynaptic terminals.
Copyright © 2019 Elsevier Ltd. All rights reserved.

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Year:  2019        PMID: 30784979      PMCID: PMC6919308          DOI: 10.1016/j.conb.2019.01.020

Source DB:  PubMed          Journal:  Curr Opin Neurobiol        ISSN: 0959-4388            Impact factor:   6.627


  81 in total

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2.  Action potentials and frequency-dependent secretion in the mouse neurohypophysis.

Authors:  H Gainer; S A Wolfe; A L Obaid; B M Salzberg
Journal:  Neuroendocrinology       Date:  1986       Impact factor: 4.914

3.  Differential Control of Axonal and Somatic Resting Potential by Voltage-Dependent Conductances in Cortical Layer 5 Pyramidal Neurons.

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Journal:  Neuron       Date:  2018-03-08       Impact factor: 17.173

4.  Subcellular Imaging of Voltage and Calcium Signals Reveals Neural Processing In Vivo.

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Review 5.  Mechanisms of sodium channel clustering and its influence on axonal impulse conduction.

Authors:  Sean A Freeman; Anne Desmazières; Desdemona Fricker; Catherine Lubetzki; Nathalie Sol-Foulon
Journal:  Cell Mol Life Sci       Date:  2015-10-29       Impact factor: 9.261

6.  Presynaptic hyperpolarization induces a fast analogue modulation of spike-evoked transmission mediated by axonal sodium channels.

Authors:  Sylvain Rama; Mickaël Zbili; Andrzej Bialowas; Laure Fronzaroli-Molinieres; Norbert Ankri; Edmond Carlier; Vincenzo Marra; Dominique Debanne
Journal:  Nat Commun       Date:  2015-12-10       Impact factor: 14.919

7.  Ankyrin G Membrane Partners Drive the Establishment and Maintenance of the Axon Initial Segment.

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Journal:  Front Cell Neurosci       Date:  2017-01-26       Impact factor: 5.505

8.  Kv1.1 channelopathy abolishes presynaptic spike width modulation by subthreshold somatic depolarization.

Authors:  Umesh Vivekananda; Pavel Novak; Oscar D Bello; Yuri E Korchev; Shyam S Krishnakumar; Kirill E Volynski; Dimitri M Kullmann
Journal:  Proc Natl Acad Sci U S A       Date:  2017-02-13       Impact factor: 11.205

9.  Neuron Morphology Influences Axon Initial Segment Plasticity.

Authors:  Allan T Gulledge; Jaime J Bravo
Journal:  eNeuro       Date:  2016-02-13

10.  Loss of Saltation and Presynaptic Action Potential Failure in Demyelinated Axons.

Authors:  Mustafa S Hamada; Marko A Popovic; Maarten H P Kole
Journal:  Front Cell Neurosci       Date:  2017-02-27       Impact factor: 5.505

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  4 in total

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2.  Editorial overview: Molecular neuroscience.

Authors:  Timothy A Ryan; Yishi Jin
Journal:  Curr Opin Neurobiol       Date:  2019-06-30       Impact factor: 6.627

3.  Selective axonal transport through branch junctions is directed by growth cone signaling and mediated by KIF1/kinesin-3 motors.

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4.  Kv1.1 channels mediate network excitability and feed-forward inhibition in local amygdala circuits.

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  4 in total

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