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A New TASK for Dipeptidyl Peptidase-like Protein 6

Dipeptidyl Peptidase-like Protein 6 (DPP6) is widely expressed in the brain where it co-assembles with Kv4 channels and KChIP auxiliary subunits to regulate the amplitude and functional properties of the somatodendritic A-current, I(SA). Here we show that in cerebellar granule (CG) cells DPP6 also r...

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Autores principales: Nadin, Brian M., Pfaffinger, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621905/
https://www.ncbi.nlm.nih.gov/pubmed/23593319
http://dx.doi.org/10.1371/journal.pone.0060831
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author Nadin, Brian M.
Pfaffinger, Paul J.
author_facet Nadin, Brian M.
Pfaffinger, Paul J.
author_sort Nadin, Brian M.
collection PubMed
description Dipeptidyl Peptidase-like Protein 6 (DPP6) is widely expressed in the brain where it co-assembles with Kv4 channels and KChIP auxiliary subunits to regulate the amplitude and functional properties of the somatodendritic A-current, I(SA). Here we show that in cerebellar granule (CG) cells DPP6 also regulates resting membrane potential and input resistance by increasing the amplitude of the I(K(SO)) resting membrane current. Pharmacological analysis shows that DPP6 acts through the control of a channel with properties matching the K(2P) channel TASK-3. Heterologous expression and co-immunoprecipitation shows that DPP6 co-expression with TASK-3 results in the formation of a protein complex that enhances resting membrane potassium conductance. The co-regulation of resting and voltage-gated channels by DPP6 produces coordinate shifts in resting membrane potential and A-current gating that optimize the sensitivity of I(SA) inactivation gating to subthreshold fluctuations in resting membrane potential.
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spelling pubmed-36219052013-04-16 A New TASK for Dipeptidyl Peptidase-like Protein 6 Nadin, Brian M. Pfaffinger, Paul J. PLoS One Research Article Dipeptidyl Peptidase-like Protein 6 (DPP6) is widely expressed in the brain where it co-assembles with Kv4 channels and KChIP auxiliary subunits to regulate the amplitude and functional properties of the somatodendritic A-current, I(SA). Here we show that in cerebellar granule (CG) cells DPP6 also regulates resting membrane potential and input resistance by increasing the amplitude of the I(K(SO)) resting membrane current. Pharmacological analysis shows that DPP6 acts through the control of a channel with properties matching the K(2P) channel TASK-3. Heterologous expression and co-immunoprecipitation shows that DPP6 co-expression with TASK-3 results in the formation of a protein complex that enhances resting membrane potassium conductance. The co-regulation of resting and voltage-gated channels by DPP6 produces coordinate shifts in resting membrane potential and A-current gating that optimize the sensitivity of I(SA) inactivation gating to subthreshold fluctuations in resting membrane potential. Public Library of Science 2013-04-09 /pmc/articles/PMC3621905/ /pubmed/23593319 http://dx.doi.org/10.1371/journal.pone.0060831 Text en © 2013 Nadin, Pfaffinger http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nadin, Brian M.
Pfaffinger, Paul J.
A New TASK for Dipeptidyl Peptidase-like Protein 6
title A New TASK for Dipeptidyl Peptidase-like Protein 6
title_full A New TASK for Dipeptidyl Peptidase-like Protein 6
title_fullStr A New TASK for Dipeptidyl Peptidase-like Protein 6
title_full_unstemmed A New TASK for Dipeptidyl Peptidase-like Protein 6
title_short A New TASK for Dipeptidyl Peptidase-like Protein 6
title_sort new task for dipeptidyl peptidase-like protein 6
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621905/
https://www.ncbi.nlm.nih.gov/pubmed/23593319
http://dx.doi.org/10.1371/journal.pone.0060831
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