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Pannexin 2 protein expression is not restricted to the CNS

Pannexins (Panx) are proteins homologous to the invertebrate gap junction proteins called innexins (Inx) and are traditionally described as transmembrane channels connecting the intracellular and extracellular compartments. Three distinct Panx paralogs (Panx1, Panx2 and Panx3) have been identified i...

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Autores principales: Le Vasseur, Maxence, Lelowski, Jonathan, Bechberger, John F., Sin, Wun-Chey, Naus, Christian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243559/
https://www.ncbi.nlm.nih.gov/pubmed/25505382
http://dx.doi.org/10.3389/fncel.2014.00392
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author Le Vasseur, Maxence
Lelowski, Jonathan
Bechberger, John F.
Sin, Wun-Chey
Naus, Christian C.
author_facet Le Vasseur, Maxence
Lelowski, Jonathan
Bechberger, John F.
Sin, Wun-Chey
Naus, Christian C.
author_sort Le Vasseur, Maxence
collection PubMed
description Pannexins (Panx) are proteins homologous to the invertebrate gap junction proteins called innexins (Inx) and are traditionally described as transmembrane channels connecting the intracellular and extracellular compartments. Three distinct Panx paralogs (Panx1, Panx2 and Panx3) have been identified in vertebrates but previous reports on Panx expression and functionality focused primarily on Panx1 and Panx3 proteins. Several gene expression studies reported that Panx2 transcript is largely restricted to the central nervous system (CNS) hence suggesting that Panx2 might serve an important role in the CNS. However, the lack of suitable antibodies prevented the creation of a comprehensive map of Panx2 protein expression and Panx2 protein localization profile is currently mostly inferred from the distribution of its transcript. In this study, we characterized novel commercial monoclonal antibodies and surveyed Panx2 expression and distribution at the mRNA and protein level by real-time qPCR, Western blotting and immunofluorescence. Panx2 protein levels were readily detected in every tissue examined, even when transcriptional analysis predicted very low Panx2 protein expression. Furthermore, our results indicate that Panx2 transcriptional activity is a poor predictor of Panx2 protein abundance and does not correlate with Panx2 protein levels. Despite showing disproportionately high transcript levels, the CNS expressed less Panx2 protein than any other tissues analyzed. Additionally, we showed that Panx2 protein does not localize at the plasma membrane like other gap junction proteins but remains confined within cytoplasmic compartments. Overall, our results demonstrate that the endogenous expression of Panx2 protein is not restricted to the CNS and is more ubiquitous than initially predicted.
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spelling pubmed-42435592014-12-10 Pannexin 2 protein expression is not restricted to the CNS Le Vasseur, Maxence Lelowski, Jonathan Bechberger, John F. Sin, Wun-Chey Naus, Christian C. Front Cell Neurosci Neuroscience Pannexins (Panx) are proteins homologous to the invertebrate gap junction proteins called innexins (Inx) and are traditionally described as transmembrane channels connecting the intracellular and extracellular compartments. Three distinct Panx paralogs (Panx1, Panx2 and Panx3) have been identified in vertebrates but previous reports on Panx expression and functionality focused primarily on Panx1 and Panx3 proteins. Several gene expression studies reported that Panx2 transcript is largely restricted to the central nervous system (CNS) hence suggesting that Panx2 might serve an important role in the CNS. However, the lack of suitable antibodies prevented the creation of a comprehensive map of Panx2 protein expression and Panx2 protein localization profile is currently mostly inferred from the distribution of its transcript. In this study, we characterized novel commercial monoclonal antibodies and surveyed Panx2 expression and distribution at the mRNA and protein level by real-time qPCR, Western blotting and immunofluorescence. Panx2 protein levels were readily detected in every tissue examined, even when transcriptional analysis predicted very low Panx2 protein expression. Furthermore, our results indicate that Panx2 transcriptional activity is a poor predictor of Panx2 protein abundance and does not correlate with Panx2 protein levels. Despite showing disproportionately high transcript levels, the CNS expressed less Panx2 protein than any other tissues analyzed. Additionally, we showed that Panx2 protein does not localize at the plasma membrane like other gap junction proteins but remains confined within cytoplasmic compartments. Overall, our results demonstrate that the endogenous expression of Panx2 protein is not restricted to the CNS and is more ubiquitous than initially predicted. Frontiers Media S.A. 2014-11-25 /pmc/articles/PMC4243559/ /pubmed/25505382 http://dx.doi.org/10.3389/fncel.2014.00392 Text en Copyright © 2014 Le Vasseur, Lelowski, Bechberger, Sin and Naus. 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 and reproduction in other forums is permitted, provided the original author(s) or licensor 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
Le Vasseur, Maxence
Lelowski, Jonathan
Bechberger, John F.
Sin, Wun-Chey
Naus, Christian C.
Pannexin 2 protein expression is not restricted to the CNS
title Pannexin 2 protein expression is not restricted to the CNS
title_full Pannexin 2 protein expression is not restricted to the CNS
title_fullStr Pannexin 2 protein expression is not restricted to the CNS
title_full_unstemmed Pannexin 2 protein expression is not restricted to the CNS
title_short Pannexin 2 protein expression is not restricted to the CNS
title_sort pannexin 2 protein expression is not restricted to the cns
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243559/
https://www.ncbi.nlm.nih.gov/pubmed/25505382
http://dx.doi.org/10.3389/fncel.2014.00392
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