Evidence map›Paper›PMID 21719736›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2011

Acid secretion-associated translocation of KCNJ15 in gastric parietal cells.

Wenjun He, Wensheng Liu, Catherine S Chew, Susan S Baker, Robert D Baker, John G Forte, Lixin Zhu

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  5. NaFrontiers in physiology · 2023
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  8. Loss ofCancer management and research · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Wenjun HeDigestive Diseases and Nutrition Center, Dept. of Pediatrics, State Univ. of New York at Buffalo, USA.
Wensheng Liu
Catherine S Chew
Susan S Baker
Robert D Baker
John G Forte
Lixin Zhu
University at Buffalo, State University of New York · USAugusta University · USUniversity of California, Berkeley · US

Funding

MECHANISMS OF HCL TRANSPORT BY GASTRIC MUCOSAR01DK010141 · NIDDK · UNIVERSITY OF CALIFORNIA BERKELEY · PI MACHEN, TERRY E · 1986 to 2013
$2.9M
GASTRIC H+ ION TRANSPORT-CELLULAR CONTROL MECHANSIMSR01DK031900 · NIDDK · MOREHOUSE SCHOOL OF MEDICINE · PI CHEW, CATHERINE S · 1986 to 2008
$2.3M
MECHANISMS OF HCL TRANSPORT BY GASTRIC MUCOSAR37DK010141 · NIDDK · UNIVERSITY OF CALIFORNIA BERKELEY · PI FORTE, JOHN G · 1996 to 2003
$1.1M
GASTRIC HYDROGEN TRANSPORT--CELLULAR CONTROL MECHANISMSR37DK031900 · NIDDK · MOREHOUSE SCHOOL OF MEDICINE · PI CHEW, CATHERINE S · 1992 to 1999
–
NIDDK NIH HHS DK010141-42NIDDK NIH HHS DK31900NIDDK NIH HHS R01 DK031900NIDDK NIH HHS R37 DK031900
6 · The paper itself

Abstract

Potassium ions are required for gastric acid secretion. Several potassium channels have been implicated in providing K(+) at the apical membrane of parietal cells. In examining the mRNA expression levels between gastric mucosa and liver tissue, KCNJ15 stood out as the most highly specific K(+) channel in the gastric mucosa. Western blot analysis confirmed that KCNJ15 is abundant in the stomach. Immunofluorescence staining of isolated gastric glands indicated that KCNJ15 was expressed in parietal cells and chief cells, but not in mucous neck cells. In resting parietal cells, KCNJ15 was mainly found in puncta throughout the cytoplasm but was distinct from H(+)-K(+)-ATPase. Upon stimulation, KCNJ15 and H(+)-K(+)-ATPase become colocalized on the apical membranes, as suggested by immunofluorescence staining. Western blot analysis of the resting and the stimulated membrane fractions confirmed this observation. From nonsecreting preparations, KCNJ15-containing vesicles sedimented after a 4-h centrifugation at 100,000 g, but not after a 30-min spin, which did sediment most of the H(+)-K(+)-ATPase-containing tubulovesicles. Most of the KCNJ15 containing small vesicle population was depleted upon stimulation of parietal cells, as indicated by the fact that the KCNJ15 signal was shifted to a large membrane fraction that sedimented at 4,000 g. Our results demonstrate that, in nonsecreting parietal cells, KCNJ15 is stored in vesicles distinct from the H(+)-K(+)-ATPase-enriched tubulovesicles. Furthermore, upon stimulation, KCNJ15 and H(+)-K(+)-ATPase both translocate to the apical membrane for active acid secretion. Thus KCNJ15 can be added to the family of apical K(+) channels in gastric parietal cells.

Indexed as

AminopyrineAnimalsHEK293 CellsH(+)-K(+)-Exchanging ATPaseHumansMiceParietal Cells, GastricPotassium Channels, Inwardly RectifyingRabbitsRNA, MessengerAminopyrineH(+)-K(+)-Exchanging ATPaseKir4.2 channelPotassium Channels, Inwardly RectifyingRNA, Messenger

Identifiers

PMID21719736
PMCPMC3191558
OpenAlexW1975637590

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.