Pannexin 2 protein expression is not restricted to the CNS

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

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Main Authors: Maxence eLe Vasseur, Jonathan eLelowski, John eBechberger, Wun-Chey eSin, Christian eNaus
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-11-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00392/full
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spelling doaj-3a48c0f9d5764a76a1e623d668b2c22a2020-11-25T01:27:50ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022014-11-01810.3389/fncel.2014.00392113420Pannexin 2 protein expression is not restricted to the CNSMaxence eLe Vasseur0Jonathan eLelowski1John eBechberger2Wun-Chey eSin3Christian eNaus4University of British ColumbiaUniversity of British ColumbiaUniversity of British ColumbiaUniversity of British ColumbiaUniversity of British ColumbiaPannexins are proteins homologous to the invertebrate gap junction proteins called innexins and are traditionally described as transmembrane channels connecting the intracellular and extracellular compartments. Three distinct pannexin paralogs (Panx1, Panx2 and Panx3) have been identified in vertebrates but previous reports on pannexin 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.http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00392/fullMousemRNAprotein expressiongap junctiongene transcriptionProtein distribution
collection DOAJ
language English
format Article
sources DOAJ
author Maxence eLe Vasseur
Jonathan eLelowski
John eBechberger
Wun-Chey eSin
Christian eNaus
spellingShingle Maxence eLe Vasseur
Jonathan eLelowski
John eBechberger
Wun-Chey eSin
Christian eNaus
Pannexin 2 protein expression is not restricted to the CNS
Frontiers in Cellular Neuroscience
Mouse
mRNA
protein expression
gap junction
gene transcription
Protein distribution
author_facet Maxence eLe Vasseur
Jonathan eLelowski
John eBechberger
Wun-Chey eSin
Christian eNaus
author_sort Maxence eLe Vasseur
title Pannexin 2 protein expression is not restricted to the CNS
title_short 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_sort pannexin 2 protein expression is not restricted to the cns
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2014-11-01
description Pannexins are proteins homologous to the invertebrate gap junction proteins called innexins and are traditionally described as transmembrane channels connecting the intracellular and extracellular compartments. Three distinct pannexin paralogs (Panx1, Panx2 and Panx3) have been identified in vertebrates but previous reports on pannexin 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.
topic Mouse
mRNA
protein expression
gap junction
gene transcription
Protein distribution
url http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00392/full
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