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Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions
Aquaporin 5 (AQP5) plays an important role in the salivary gland function. The mRNA and protein for AQP5 are expressed in the acini from embryonic days E13-16 and E17-18, respectively and for entire postnatal days. Ligation-reopening of main excretory duct induces changes in the AQP5 level which wou...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072788/ https://www.ncbi.nlm.nih.gov/pubmed/32053992 http://dx.doi.org/10.3390/ijms21041182 |
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author | Hosoi, Kazuo Yao, Chenjuan Hasegawa, Takahiro Yoshimura, Hiroshi Akamatsu, Tetsuya |
author_facet | Hosoi, Kazuo Yao, Chenjuan Hasegawa, Takahiro Yoshimura, Hiroshi Akamatsu, Tetsuya |
author_sort | Hosoi, Kazuo |
collection | PubMed |
description | Aquaporin 5 (AQP5) plays an important role in the salivary gland function. The mRNA and protein for AQP5 are expressed in the acini from embryonic days E13-16 and E17-18, respectively and for entire postnatal days. Ligation-reopening of main excretory duct induces changes in the AQP5 level which would give an insight for mechanism of regeneration/self-duplication of acinar cells. The AQP5 level in the submandibular gland (SMG) decreases by chorda tympani denervation (CTD) via activation autophagosome, suggesting that its level in the SMG under normal condition is maintained by parasympathetic nerve. Isoproterenol (IPR), a β-adrenergic agonist, raised the levels of membrane AQP5 protein and its mRNA in the parotid gland (PG), suggesting coupling of the AQP5 dynamic and amylase secretion-restoration cycle. In the PG, lipopolysaccharide (LPS) is shown to activate mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-κB) signalings and potentially downregulate AQP5 expression via cross coupling of activator protein-1 (AP-1) and NF-κB. In most species, Ser-156 and Thr-259 of AQP5 are experimentally phosphorylated, which is enhanced by cAMP analogues and forskolin. cAMP-dependent phosphorylation of AQP5 does not seem to be markedly involved in regulation of its intracellular trafficking but seems to play a role in its constitutive expression and lateral diffusion in the cell membrane. Additionally, Ser-156 phosphorylation may be important for cancer development. |
format | Online Article Text |
id | pubmed-7072788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70727882020-03-19 Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions Hosoi, Kazuo Yao, Chenjuan Hasegawa, Takahiro Yoshimura, Hiroshi Akamatsu, Tetsuya Int J Mol Sci Review Aquaporin 5 (AQP5) plays an important role in the salivary gland function. The mRNA and protein for AQP5 are expressed in the acini from embryonic days E13-16 and E17-18, respectively and for entire postnatal days. Ligation-reopening of main excretory duct induces changes in the AQP5 level which would give an insight for mechanism of regeneration/self-duplication of acinar cells. The AQP5 level in the submandibular gland (SMG) decreases by chorda tympani denervation (CTD) via activation autophagosome, suggesting that its level in the SMG under normal condition is maintained by parasympathetic nerve. Isoproterenol (IPR), a β-adrenergic agonist, raised the levels of membrane AQP5 protein and its mRNA in the parotid gland (PG), suggesting coupling of the AQP5 dynamic and amylase secretion-restoration cycle. In the PG, lipopolysaccharide (LPS) is shown to activate mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-κB) signalings and potentially downregulate AQP5 expression via cross coupling of activator protein-1 (AP-1) and NF-κB. In most species, Ser-156 and Thr-259 of AQP5 are experimentally phosphorylated, which is enhanced by cAMP analogues and forskolin. cAMP-dependent phosphorylation of AQP5 does not seem to be markedly involved in regulation of its intracellular trafficking but seems to play a role in its constitutive expression and lateral diffusion in the cell membrane. Additionally, Ser-156 phosphorylation may be important for cancer development. MDPI 2020-02-11 /pmc/articles/PMC7072788/ /pubmed/32053992 http://dx.doi.org/10.3390/ijms21041182 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hosoi, Kazuo Yao, Chenjuan Hasegawa, Takahiro Yoshimura, Hiroshi Akamatsu, Tetsuya Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions |
title | Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions |
title_full | Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions |
title_fullStr | Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions |
title_full_unstemmed | Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions |
title_short | Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions |
title_sort | dynamics of salivary gland aqp5 under normal and pathologic conditions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072788/ https://www.ncbi.nlm.nih.gov/pubmed/32053992 http://dx.doi.org/10.3390/ijms21041182 |
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