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Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia

Pannexins are a family of transmembrane nonselective channel proteins that participate in the release of ATP into extracellular space. Previous studies have suggested that pannexin‐1 (Panx1) may constitute a local autocrine/paracrine system via transmitter ATP in association with the purinergic P2X7...

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Autores principales: Ohbuchi, Toyoaki, Takenaga, Fumiko, Hohchi, Nobusuke, Wakasugi, Tetsuro, Ueta, Yoichi, Suzuki, Hideaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966237/
https://www.ncbi.nlm.nih.gov/pubmed/24744896
http://dx.doi.org/10.1002/phy2.227
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author Ohbuchi, Toyoaki
Takenaga, Fumiko
Hohchi, Nobusuke
Wakasugi, Tetsuro
Ueta, Yoichi
Suzuki, Hideaki
author_facet Ohbuchi, Toyoaki
Takenaga, Fumiko
Hohchi, Nobusuke
Wakasugi, Tetsuro
Ueta, Yoichi
Suzuki, Hideaki
author_sort Ohbuchi, Toyoaki
collection PubMed
description Pannexins are a family of transmembrane nonselective channel proteins that participate in the release of ATP into extracellular space. Previous studies have suggested that pannexin‐1 (Panx1) may constitute a local autocrine/paracrine system via transmitter ATP in association with the purinergic P2X7 receptor. In this study, we investigate the expressions of Panx1 and P2X7 in human nasal mucosa, together with hypotonic stress‐induced ATP release from this tissue. Twenty men and one woman ranging in age from 10 to 82 years with an average age of 44.2 ± 4.4 years participated in the study. Inferior turbinates were collected from patients with chronic hypertrophic rhinitis during endoscopic endonasal surgery. The expressions of Panx1 and P2X7 were examined by fluorescence immunohistochemistry and quantitative reverse transcription‐polymerase chain reaction (qRT‐PCR). We also examined hypotonic stress‐induced ATP release from the turbinate mucosa and the effects of channel blockers in an ex vivo experiment. Substantial expressions of both proteins were observed in human nasal mucosa. The immunoreactivity for Panx1 was stronger than that for P2X7. The presence of the transcripts of Panx1 and P2X7 was also shown by qRT‐PCR. Ten and 100 μmol/L carbenoxolone (a Panx1 channel blocker) significantly inhibited the ATP release from the nasal mucosa, but flufenamic acid (a connexin channel blocker) and gadolinium (a stretch‐activated channel blocker) did not. These results indicate the coexistence of Panx1 and P2X7 in, and Panx1‐dependent ATP release from, the human nasal mucosa, suggesting the possible participation of these molecules in the physiological functions of the upper airway.
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spelling pubmed-39662372014-03-31 Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia Ohbuchi, Toyoaki Takenaga, Fumiko Hohchi, Nobusuke Wakasugi, Tetsuro Ueta, Yoichi Suzuki, Hideaki Physiol Rep Original Research Pannexins are a family of transmembrane nonselective channel proteins that participate in the release of ATP into extracellular space. Previous studies have suggested that pannexin‐1 (Panx1) may constitute a local autocrine/paracrine system via transmitter ATP in association with the purinergic P2X7 receptor. In this study, we investigate the expressions of Panx1 and P2X7 in human nasal mucosa, together with hypotonic stress‐induced ATP release from this tissue. Twenty men and one woman ranging in age from 10 to 82 years with an average age of 44.2 ± 4.4 years participated in the study. Inferior turbinates were collected from patients with chronic hypertrophic rhinitis during endoscopic endonasal surgery. The expressions of Panx1 and P2X7 were examined by fluorescence immunohistochemistry and quantitative reverse transcription‐polymerase chain reaction (qRT‐PCR). We also examined hypotonic stress‐induced ATP release from the turbinate mucosa and the effects of channel blockers in an ex vivo experiment. Substantial expressions of both proteins were observed in human nasal mucosa. The immunoreactivity for Panx1 was stronger than that for P2X7. The presence of the transcripts of Panx1 and P2X7 was also shown by qRT‐PCR. Ten and 100 μmol/L carbenoxolone (a Panx1 channel blocker) significantly inhibited the ATP release from the nasal mucosa, but flufenamic acid (a connexin channel blocker) and gadolinium (a stretch‐activated channel blocker) did not. These results indicate the coexistence of Panx1 and P2X7 in, and Panx1‐dependent ATP release from, the human nasal mucosa, suggesting the possible participation of these molecules in the physiological functions of the upper airway. Wiley Periodicals, Inc. 2014-02-10 /pmc/articles/PMC3966237/ /pubmed/24744896 http://dx.doi.org/10.1002/phy2.227 Text en © 2014 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Ohbuchi, Toyoaki
Takenaga, Fumiko
Hohchi, Nobusuke
Wakasugi, Tetsuro
Ueta, Yoichi
Suzuki, Hideaki
Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia
title Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia
title_full Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia
title_fullStr Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia
title_full_unstemmed Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia
title_short Possible contribution of pannexin‐1 to ATP release in human upper airway epithelia
title_sort possible contribution of pannexin‐1 to atp release in human upper airway epithelia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966237/
https://www.ncbi.nlm.nih.gov/pubmed/24744896
http://dx.doi.org/10.1002/phy2.227
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