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Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways

Neuronal growth factors regulate the expression of voltage-activated sodium current in differentiating sympathetic neurons and PC12 cells. We show that, in PC12 cells, the NGF- and FGF-induced sodium current results from increased expression of two distinct sodium channel types. Sodium current resul...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119579/
https://www.ncbi.nlm.nih.gov/pubmed/8394370
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collection PubMed
description Neuronal growth factors regulate the expression of voltage-activated sodium current in differentiating sympathetic neurons and PC12 cells. We show that, in PC12 cells, the NGF- and FGF-induced sodium current results from increased expression of two distinct sodium channel types. Sodium current results from the rapid induction of a novel sodium channel transcript, also found in peripheral neurons, and from the long term induction of brain type II/IIA mRNA. Expression of the type II/IIA sodium channel requires activation of the cyclic AMP-dependent protein kinase (A-kinase), whereas induction of the peripheral neuron type sodium channel occurs through an A-kinase-independent signal transduction pathway. These findings suggest that the two sodium channel types act in concert to ensure the generation of action potentials during neuronal differentiation.
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spelling pubmed-21195792008-05-01 Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways J Cell Biol Articles Neuronal growth factors regulate the expression of voltage-activated sodium current in differentiating sympathetic neurons and PC12 cells. We show that, in PC12 cells, the NGF- and FGF-induced sodium current results from increased expression of two distinct sodium channel types. Sodium current results from the rapid induction of a novel sodium channel transcript, also found in peripheral neurons, and from the long term induction of brain type II/IIA mRNA. Expression of the type II/IIA sodium channel requires activation of the cyclic AMP-dependent protein kinase (A-kinase), whereas induction of the peripheral neuron type sodium channel occurs through an A-kinase-independent signal transduction pathway. These findings suggest that the two sodium channel types act in concert to ensure the generation of action potentials during neuronal differentiation. The Rockefeller University Press 1993-08-02 /pmc/articles/PMC2119579/ /pubmed/8394370 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways
title Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways
title_full Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways
title_fullStr Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways
title_full_unstemmed Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways
title_short Neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways
title_sort neuronal growth factor regulation of two different sodium channel types through distinct signal transduction pathways
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119579/
https://www.ncbi.nlm.nih.gov/pubmed/8394370