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Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions

Identifieur interne : 000168 ( an2020/Analysis ); précédent : 000167; suivant : 000169

Dynamics of Salivary Gland AQP5 under Normal and Pathologic Conditions

Auteurs : Kazuo Hosoi [Japon] ; Chenjuan Yao ; Takahiro Hasegawa ; Hiroshi Yoshimura ; Tetsuya Akamatsu [Japon]

Source :

RBID : PMC:7072788

Abstract

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.


Url:
DOI: 10.3390/ijms21041182
PubMed: 32053992
PubMed Central: 7072788


Affiliations:


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PMC:7072788

Le document en format XML

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<p>Aquaporin 5 (AQP5) plays an important role in the salivary gland function. The
<italic>mRNA</italic>
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
<italic>mRNA</italic>
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.</p>
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<author>
<name sortKey="Antunes, F" uniqKey="Antunes F">F. Antunes</name>
</author>
<author>
<name sortKey="Gasparovic, A C" uniqKey="Gasparovic A">A.C. Gasparovic</name>
</author>
<author>
<name sortKey="Soveral, G" uniqKey="Soveral G">G. Soveral</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Satoh, K" uniqKey="Satoh K">K. Satoh</name>
</author>
<author>
<name sortKey="Narita, T" uniqKey="Narita T">T. Narita</name>
</author>
<author>
<name sortKey="Matsuki Fukushima, M" uniqKey="Matsuki Fukushima M">M. Matsuki-Fukushima</name>
</author>
<author>
<name sortKey="Okabayashi, K" uniqKey="Okabayashi K">K. Okabayashi</name>
</author>
<author>
<name sortKey="Ito, T" uniqKey="Ito T">T. Ito</name>
</author>
<author>
<name sortKey="Senpuku, H" uniqKey="Senpuku H">H. Senpuku</name>
</author>
<author>
<name sortKey="Sugiya, H" uniqKey="Sugiya H">H. Sugiya</name>
</author>
</analytic>
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</div1>
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</TEI>
<affiliations>
<list>
<country>
<li>Japon</li>
</country>
</list>
<tree>
<noCountry>
<name sortKey="Hasegawa, Takahiro" sort="Hasegawa, Takahiro" uniqKey="Hasegawa T" first="Takahiro" last="Hasegawa">Takahiro Hasegawa</name>
<name sortKey="Yao, Chenjuan" sort="Yao, Chenjuan" uniqKey="Yao C" first="Chenjuan" last="Yao">Chenjuan Yao</name>
<name sortKey="Yoshimura, Hiroshi" sort="Yoshimura, Hiroshi" uniqKey="Yoshimura H" first="Hiroshi" last="Yoshimura">Hiroshi Yoshimura</name>
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<name sortKey="Hosoi, Kazuo" sort="Hosoi, Kazuo" uniqKey="Hosoi K" first="Kazuo" last="Hosoi">Kazuo Hosoi</name>
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<name sortKey="Akamatsu, Tetsuya" sort="Akamatsu, Tetsuya" uniqKey="Akamatsu T" first="Tetsuya" last="Akamatsu">Tetsuya Akamatsu</name>
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