Evidence map›Paper›PMID 22138972›Full record

ArticlePflugers Archiv : European journal of physiology2012

NHE1 activity contributes to migration and is necessary for proliferation of human gastric myofibroblasts.

Mátyás Czepán, Zoltán Rakonczay, Andrea Varró, Islay Steele, Rod Dimaline, Nantaporn Lertkowit, János Lonovics, Andrea Schnúr, György Biczó, Andrea Geisz and 5 more

Abstract read
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In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. (Patho-)Physiology of NaFrontiers in physiology · 2019
    Review
  7. Article
  8. Pathophysiology of Intestinal NaCellular and molecular gastroenterology and hepatology · 2017
    Article
  9. Article
  10. Distinct miRNA profiles in normal and gastric cancer myofibroblasts and significance in Wnt signaling.American journal of physiology. Gastrointestinal and liver physiology · 2016
    Article
  11. Article
  12. 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

15 authors at 2 institutions in 2 countries.

Mátyás CzepánFirst Department of Medicine, University of Szeged, 6720, Korányi fasor 8-10, Szeged, Hungary.
Zoltán Rakonczay
Andrea Varró
Islay Steele
Rod Dimaline
Nantaporn Lertkowit
János Lonovics
Andrea Schnúr
György Biczó
Andrea Geisz
György Lázár
Zsolt Simonka
Viktória Venglovecz
Tibor Wittmann
Péter Hegyi
University of Szeged · HUUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myofibroblasts play central roles in wound healing, deposition of the extracellular matrix and epithelial function. Their functions depend on migration and proliferation within the subepithelial matrix, which results in accelerated cellular metabolism. Upregulated metabolic pathways generate protons which need to be excreted to maintain intracellular pH (pH(i)). We isolated human gastric myofibroblasts (HGMs) from surgical specimens of five patients. Then we characterized, for the first time, the expression and functional activities of the Na(+)/H(+) exchanger (NHE) isoforms 1, 2 and 3, and the functional activities of the Na(+)/HCO(3)(-) cotransporter (NBC) and the anion exchanger (AE) in cultured HGMs using microfluorimetry, immunocytochemistry, reverse transcription polymerase chain reaction and immunoblot analysis. We showed that NHE1-3, NBC and AE activities are present in HGMs and that NHE1 is the most active of the NHEs. In scratch wound assays we also demonstrated (using the selective NHE inhibitor HOE-642) that carbachol and insulin like growth factor II (IGF-II) partly stimulate migration of HGMs in a NHE1-dependent manner. EdU incorporation assays revealed that IGF-II induces proliferation of HGMs which is inhibited by HOE-642. The results indicate that NHE1 is necessary for IGF-II-induced proliferation response of HGMs. Overall, we have characterized the pH(i) regulatory mechanisms of HGMs. In addition, we demonstrated that NHE1 activity contributes to both IGF-II- and carbachol-stimulated migration and that it is obligatory for IGF-II-induced proliferation of HGMs.

Indexed as

AdultAgedAntiportersCarbacholCation Transport ProteinsCell MovementCell ProliferationFemaleGuanidinesHumansHydrogen-Ion ConcentrationInsulin-Like Growth Factor IIMaleMyofibroblastsSodium-Bicarbonate SymportersSodium-Hydrogen Exchanger 1AntiportersCarbacholcariporideCation Transport ProteinsGuanidinesInsulin-Like Growth Factor IISLC9A1 protein, humanSLC9A2 protein, humanSodium-Bicarbonate SymportersSodium-Hydrogen Exchanger 1Sodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersSulfones

Identifiers

PMID22138972
OpenAlexW2078820501

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.