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Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3

TRPM4 is a Ca(2+)-activated non-selective cationic channel that conducts monovalent cations. TRPM4 has been proposed to contribute to burst firing and sustained activity in several brain regions, however, the cellular and subcellular pattern of TRPM4 expression in medial prefrontal cortex (mPFC) dur...

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Autores principales: Riquelme, Denise, Silva, Ian, Philp, Ashleigh M., Huidobro-Toro, Juan P., Cerda, Oscar, Trimmer, James S., Leiva-Salcedo, Elias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797675/
https://www.ncbi.nlm.nih.gov/pubmed/29440991
http://dx.doi.org/10.3389/fncel.2018.00012
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author Riquelme, Denise
Silva, Ian
Philp, Ashleigh M.
Huidobro-Toro, Juan P.
Cerda, Oscar
Trimmer, James S.
Leiva-Salcedo, Elias
author_facet Riquelme, Denise
Silva, Ian
Philp, Ashleigh M.
Huidobro-Toro, Juan P.
Cerda, Oscar
Trimmer, James S.
Leiva-Salcedo, Elias
author_sort Riquelme, Denise
collection PubMed
description TRPM4 is a Ca(2+)-activated non-selective cationic channel that conducts monovalent cations. TRPM4 has been proposed to contribute to burst firing and sustained activity in several brain regions, however, the cellular and subcellular pattern of TRPM4 expression in medial prefrontal cortex (mPFC) during postnatal development has not been elucidated. Here, we use multiplex immunofluorescence labeling of brain sections to characterize the postnatal developmental expression of TRPM4 in the mouse mPFC. We also performed electrophysiological recordings to correlate the expression of TRPM4 immunoreactivity with the presence of TRPM4-like currents. We found that TRPM4 is expressed from the first postnatal day, with expression increasing up to postnatal day 35. Additionally, in perforated patch clamp experiments, we found that TRPM4-like currents were active at resting membrane potentials at all postnatal ages studied. Moreover, TRPM4 is expressed in both pyramidal neurons and interneurons. TRPM4 expression is localized in the soma and proximal dendrites, but not in the axon initial segment of pyramidal neurons. This subcellular localization is consistent with a reduction in the basal current only when we locally perfused 9-Phenanthrol in the soma, but not upon perfusion in the medial or distal dendrites. Our results show a specific localization of TRPM4 expression in neurons in the mPFC and that a 9-Phenanthrol sensitive current is active at resting membrane potential, suggesting specific functional roles in mPFC neurons during postnatal development and in adulthood.
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spelling pubmed-57976752018-02-13 Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3 Riquelme, Denise Silva, Ian Philp, Ashleigh M. Huidobro-Toro, Juan P. Cerda, Oscar Trimmer, James S. Leiva-Salcedo, Elias Front Cell Neurosci Neuroscience TRPM4 is a Ca(2+)-activated non-selective cationic channel that conducts monovalent cations. TRPM4 has been proposed to contribute to burst firing and sustained activity in several brain regions, however, the cellular and subcellular pattern of TRPM4 expression in medial prefrontal cortex (mPFC) during postnatal development has not been elucidated. Here, we use multiplex immunofluorescence labeling of brain sections to characterize the postnatal developmental expression of TRPM4 in the mouse mPFC. We also performed electrophysiological recordings to correlate the expression of TRPM4 immunoreactivity with the presence of TRPM4-like currents. We found that TRPM4 is expressed from the first postnatal day, with expression increasing up to postnatal day 35. Additionally, in perforated patch clamp experiments, we found that TRPM4-like currents were active at resting membrane potentials at all postnatal ages studied. Moreover, TRPM4 is expressed in both pyramidal neurons and interneurons. TRPM4 expression is localized in the soma and proximal dendrites, but not in the axon initial segment of pyramidal neurons. This subcellular localization is consistent with a reduction in the basal current only when we locally perfused 9-Phenanthrol in the soma, but not upon perfusion in the medial or distal dendrites. Our results show a specific localization of TRPM4 expression in neurons in the mPFC and that a 9-Phenanthrol sensitive current is active at resting membrane potential, suggesting specific functional roles in mPFC neurons during postnatal development and in adulthood. Frontiers Media S.A. 2018-01-30 /pmc/articles/PMC5797675/ /pubmed/29440991 http://dx.doi.org/10.3389/fncel.2018.00012 Text en Copyright © 2018 Riquelme, Silva, Philp, Huidobro-Toro, Cerda, Trimmer and Leiva-Salcedo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Riquelme, Denise
Silva, Ian
Philp, Ashleigh M.
Huidobro-Toro, Juan P.
Cerda, Oscar
Trimmer, James S.
Leiva-Salcedo, Elias
Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3
title Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3
title_full Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3
title_fullStr Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3
title_full_unstemmed Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3
title_short Subcellular Localization and Activity of TRPM4 in Medial Prefrontal Cortex Layer 2/3
title_sort subcellular localization and activity of trpm4 in medial prefrontal cortex layer 2/3
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797675/
https://www.ncbi.nlm.nih.gov/pubmed/29440991
http://dx.doi.org/10.3389/fncel.2018.00012
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