Evidence map›Paper›PMID 15014914›Full record

ArticleThe Journal of membrane biology2004

Functional characterization of Na(+)/H(+) exchangers in primary cultures of prairie dog gallbladder.

S C Narins, E H Park, R Ramakrishnan, F U Garcia, J N Diven, B J Balin, C J Hammond, B R Sodam, P R Smith, M Z Abedin

Abstract read
PubMed Publisher
In one paragraph

Article in The Journal of membrane biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Pathophysiology of hepatic NaExperimental and therapeutic medicine · 2020
    Review
  3. Review
  4. Phosphorylation and subcellular localization of NaJournal of physiology and biochemistry · 2017
    Article
  5. Cholesterol gallstone disease: focusing on the role of gallbladder.Laboratory investigation; a journal of technical methods and pathology · 2015
    Review
  6. Expression and subcellular localization of NHE₃ in the human gallbladder epithelium.International journal of clinical and experimental pathology · 2014
    Article
  7. Article
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

10 authors at 3 institutions in 1 country.

S C NarinsDepartment of Surgery, Drexel University College of Medicine, Philadelphia, PA, USA.
E H Park
R Ramakrishnan
F U Garcia
J N Diven
B J Balin
C J Hammond
B R Sodam
P R Smith
M Z Abedin
Drexel University · USPhiladelphia College of Osteopathic Medicine · USUniversity of Alabama at Birmingham · US

Funding

SODIUM CHANNEL APICAL PROTEIN XENOPUS (APX) INTERACTIONSR01DK056596 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SMITH, PETER R. · 1999 to 2002
$568k
SECOND MESSENGERS, GALLBLADDER ABSORPTION AND GALLSTONESR01DK051585 · NIDDK · MCP HAHNEMANN UNIVERSITY · PI ABEDIN, MOHAMMAD Z · 1997 to 2001
$478k
NIDDK NIH HHS DK 51585NIDDK NIH HHS DK56596
6 · The paper itself

Abstract

Gallbladder Na(+) absorption is linked to gallstone formation in prairie dogs. We previously reported Na(+)/H(+) exchanger (NHE1-3) expression in native gallbladder tissues. Here we report the functional characterization of NHE1, NHE2 and NHE3 in primary cultures of prairie dog gallbladder epithelial cells (GBECs). Immunohistochemical studies showed that GBECs grown to confluency are homogeneous epithelial cells of gastrointestinal origin. Electron microscopic analysis of GBECs demonstrated that the cells form polarized monolayers characterized by tight junctions and apical microvilli. GBECs grown on Snapwells exhibited polarity and developed transepithelial short-circuit current, I(sc), (11.6 +/- 0.5 microA. cm(-2)), potential differences, V(t) (2.1 +/- 0.2 mV), and resistance, R(t) (169 +/- 12 omega. cm(2)). NHE activity in GBECs assessed by measuring dimethylamiloride-inhibitable (22)Na(+) uptake under a H(+) gradient was the same whether grown on permeable Snapwells or plastic wells. The basal rate of (22)Na(+) uptake was 21.4 +/- 1.3 nmol x mg prot(-1) x min(-1), of which 9.5 +/- 0.7 (approximately 45%) was mediated through apically-restricted NHE. Selective inhibition with HOE-694 revealed that NHE1, NHE2 and NHE3 accounted for approximately 6%, approximately 66% and approximately 28% of GBECs' total NHE activity, respectively. GBECs exhibited saturable NHE kinetics ( V(max) 9.2 +/- 0.3 nmol x mg prot(-1) x min(-1); K(m) 11.4 +/- 1.4 m M Na(+)). Expression of NHE1, NHE2 and NHE3 mRNAs was confirmed by RT-PCR analysis. These results demonstrate that the primary cultures of GBECs exhibit Na(+) transport characteristics similar to native gallbladder tissues, suggesting that these cells can be used as a tool for studying the mechanisms of gallbladder ion transport both under physiologic conditions and during gallstone formation.

Indexed as

AnimalsBiological Transport, ActiveCells, CulturedElectrophysiologyEpithelial CellsGallbladderGallstonesGene ExpressionHydrogenHydrogen-Ion ConcentrationProtein IsoformsReverse Transcriptase Polymerase Chain ReactionRNA, MessengerSciuridaeSodiumSodium-Hydrogen ExchangersHydrogenProtein IsoformsRNA, MessengerSodiumSodium-Hydrogen Exchangers

Identifiers

PMID15014914
OpenAlexW2090321877

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.