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Open AccessJournal ArticleDOI

Histamine treatment induces rearrangements of orthogonal arrays of particles (OAPs) in human AQP4-expressing gastric cells

TLDR
Cell surface biotinylation experiments confirmed that AQP4 is internalized after 20 min of histamine exposure, which may account for the downregulation of water transport, the first evidence for short term rearrangement of OAPs in an established AQP 4-expressing cell line.
Abstract
To test the involvement of the water channel aquaporin (AQP)-4 in gastric acid physiology, the human gastric cell line (HGT)-1 was stably transfected with rat AQP4. AQP4 was immunolocalized to the basolateral membrane of transfected HGT-1 cells, like in native parietal cells. Expression of AQP4 in transfected cells increased the osmotic water permeability coefficient (Pf) from 2.02 +/- 0.3 x 10-4 to 16.37 +/- 0.5 x 10-4 cm/s at 20 degrees C. Freeze-fracture EM showed distinct orthogonal arrays of particles (OAPs), the morphological signature of AQP4, on the plasma membrane of AQP4-expressing cells. Quantitative morphometry showed that the density of OAPs was 2.5 +/- 0.3% under basal condition and decreased by 50% to 1.2 +/- 0.3% after 20 min of histamine stimulation, mainly due to a significant decrease of the OAPs number. Concomitantly, Pf decreased by approximately 35% in 20-min histamine-stimulated cells. Both Pf and OAPs density were not modified after 10 min of histamine exposure, time at which the maximal hormonal response is observed. Cell surface biotinylation experiments confirmed that AQP4 is internalized after 20 min of histamine exposure, which may account for the downregulation of water transport. This is the first evidence for short term rearrangement of OAPs in an established AQP4-expressing cell line.

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Altered expression of aquaporin 4 and H+/K+-ATPase in the stomachs of peptide YY (PYY) transgenic mice

TL;DR: This study investigated the expression of AQP4 (aquaporin 4) water channel and H+/K+‐ATPase in stomachs from both control and transgenic mice to investigate the inhibitory effects of these molecules on gastrointestinal and pancreatic fluid secretion.
Journal ArticleDOI

Internalization of aquaporin-4 after collagenase-induced intracerebral hemorrhage.

TL;DR: AQP4 is internalized and the lysosome is involved in degrading the internalized AQP4 post‐ICH, which may provide biophysical insights regarding the potential of new treatments for brain edema.
Journal ArticleDOI

microRNA‐320a prevent Müller cells from hypoxia injury by targeting aquaporin‐4

TL;DR: It is indicated that miR‐320a may be a potential modulator which can mediate AQP4 expression and attenuate the hypoxia damage of Müller cells.
Journal ArticleDOI

Lysosomal degradation of retinal glial AQP4 following its internalization induced by acute ocular hypertension

TL;DR: The combined findings suggest that AQP4 is internalized in the ischemic-reperfused retina, and the lysosome is involved in degrading the internalized aquaporin-4 during the reperfusion phase.
References
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Journal ArticleDOI

Localization of MIWC and GLIP water channel homologs in neuromuscular, epithelial and glandular tissues

TL;DR: The tissue-specific expression of MIWC suggests a role in fluid transport and/or cell volume regulation in stomach and glandular epithelia, and orthogonal arrays of particles have been visualized by freeze-fracture electron microscopy, suggesting that MIWC may be the OAP protein.
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Aquaporin water channels in gastrointestinal physiology

TL;DR: Evidence that aquaporin‐type water channels are involved in GI fluid transport is evaluated and preliminary evaluation of GI function suggests a role for AQP1 in dietary fat processing and AQP4 in colonic fluid absorption.
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The Mercurial Insensitive Water Channel (AQP-4) Forms Orthogonal Arrays in Stably Transfected Chinese Hamster Ovary Cells

TL;DR: Results provide direct evidence that a molecular water channel can spontaneously assemble in regular arrays.
Journal ArticleDOI

The structural organization and protein composition of lens fiber junctions.

TL;DR: It is suggested MIP may behave as an intercellular adhesion protein which can also act as a volume-regulating channel to collapse the lens extracellular space and, in these junctions, MIP is unlikely to form gap junction-like channels.
Journal ArticleDOI

Dynamics of epithelial cells in the corpus of the mouse stomach. IV. Bidirectional migration of parietal cells ending in their gradual degeneration and loss.

TL;DR: The life story of parietal cells has been investigated in the corpus of the mouse stomach using electron microscopy and 3H‐thymidine radioautography, which indicates that the transformation of granule‐free cells into pre‐parietal cells takes at least one day.
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