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  Role of sodium channel subtype in action potential generation by neocortical pyramidal neurons

Katz, E., Stoler, O., Scheller, A., Khrapunsky, Y., Goebbels, S., Kirchhoff, F., et al. (2018). Role of sodium channel subtype in action potential generation by neocortical pyramidal neurons. Proceedings of the National Academy of Sciences of the United States of America, 115(30), E7184-E7192. doi:10.1073/pnas.1720493115.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0001-AF6F-F Version Permalink: http://hdl.handle.net/21.11116/0000-0003-CF25-B
Genre: Journal Article

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 Creators:
Katz, E., Author
Stoler, O., Author
Scheller, A., Author
Khrapunsky, Y., Author
Goebbels, S., Author
Kirchhoff, F., Author
Gutnick, M. J., Author
Wolf, Fred1, Author              
Fleidervish, I. A., Author
Affiliations:
1Research Group Theoretical Neurophysics, Max Planck Institute for Dynamics and Self-Organization, Max Planck Society, ou_2063289              

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Free keywords: Na+ flux; Nav1.6 channel; action potential; axon initial segment; conditional knockout
 Abstract: Neocortical pyramidal neurons express several distinct subtypes of voltage-gated Na+ channels. In mature cells, Nav1.6 is the dominant channel subtype in the axon initial segment (AIS) as well as in the nodes of Ranvier. Action potentials (APs) are initiated in the AIS, and it has been proposed that the high excitability of this region is related to the unique characteristics of the Nav1.6 channel. Knockout or loss-of-function mutation of the Scn8a gene is generally lethal early in life because of the importance of this subtype in noncortical regions of the nervous system. Using the Cre/loxP system, we selectively deleted Nav1.6 in excitatory neurons of the forebrain and characterized the excitability of Nav1.6-deficient layer 5 pyramidal neurons by patch-clamp and Na+ and Ca2+ imaging recordings. We now report that, in the absence of Nav1.6 expression, the AIS is occupied by Nav1.2 channels. However, APs are generated in the AIS, and differences in AP propagation to soma and dendrites are minimal. Moreover, the channels that are expressed in the AIS still show a clear hyperpolarizing shift in voltage dependence of activation, compared with somatic channels. The only major difference between Nav1.6-null and wild-type neurons was a strong reduction in persistent sodium current. We propose that the molecular environment of the AIS confers properties on whatever Na channel subtype is present and that some other benefit must be conferred by the selective axonal presence of the Nav1.6 channel.

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Language(s): eng - English
 Dates: 2018-07-242018-07-10
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: Peer
 Identifiers: DOI: 10.1073/pnas.1720493115
 Degree: -

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Title: Proceedings of the National Academy of Sciences of the United States of America
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 115 (30) Sequence Number: - Start / End Page: E7184 - E7192 Identifier: -