Evidence map›Paper›PMID 25100278›Full record

ArticleAmerican journal of physiology. Renal physiology2014

Basolateral P2X₄channels stimulate ENaC activity in Xenopus cortical collecting duct A6 cells.

Tiffany L Thai, Ling Yu, Douglas C Eaton, Billie Jean Duke, Otor Al-Khalili, Ho Yin Colin Lam, Heping Ma, Hui-Fang Bao

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. ATP release into ADPKD cysts via pannexin-1/P2X7 channels decreases ENaC activity.Biochemical and biophysical research communications · 2019
    Article
  5. Review
  6. Article
  7. Review
  8. 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

8 authors at 2 institutions in 2 countries.

Tiffany L ThaiDepartment of Physiology, Emory University, Atlanta, Georgia; and tiffany.thai@emory.edu.
Ling YuCollege of Resources and Environmental Science, Nanjing Agricultural University, Nanjing, China.
Douglas C EatonDepartment of Physiology, Emory University, Atlanta, Georgia; and.
Billie Jean DukeDepartment of Physiology, Emory University, Atlanta, Georgia; and.
Otor Al-KhaliliDepartment of Physiology, Emory University, Atlanta, Georgia; and.
Ho Yin Colin LamDepartment of Physiology, Emory University, Atlanta, Georgia; and.
Heping MaDepartment of Physiology, Emory University, Atlanta, Georgia; and.
Hui-Fang BaoDepartment of Physiology, Emory University, Atlanta, Georgia; and.
Emory University · USNanjing Agricultural University · CN

Funding

Nephrology Institutional Training Grant FLSA SupplementT32DK007656 · NIDDK · EMORY UNIVERSITY · PI SANDS, JEFF M, WALL, SUSAN MARIE · 1990 to 2020
$3.5M
MOLECULAR GENETICS OF INTESTINAL DEVELOPMENTR01DK037960 · NIDDK · WASHINGTON UNIVERSITY · PI GORDON, JEFFREY IVAN · 1987 to 1999
–
NIDDK NIH HHS R37-DK-37960NIDDK NIH HHS T32-DK-07656
6 · The paper itself

Abstract

The polarized nature of epithelial cells allows for different responses to luminal or serosal stimuli. In kidney tubules, ATP is produced luminally in response to changes in luminal flow. Luminal increases in ATP have been previously shown to inhibit the renal epithelial Na⁺ channel (ENaC). On the other hand, ATP is increased basolaterally in renal epithelia in response to aldosterone. We tested the hypothesis that basolateral ATP can stimulate ENaC function through activation of the P2X₄receptor/channel. Using single channel cell-attached patch-clamp techniques, we demonstrated the existence of a basolaterally expressed channel stimulated by the P2X₄agonist 2-methylthio-ATP (meSATP) in Xenopus A6 cells, a renal collecting duct principal cell line. This channel had a similar reversal potential and conductance to that of P2X₄channels. Cell surface biotinylation of the basolateral side of these cells confirmed the basolateral presence of the P2X4 receptor. Basolateral addition of meSATP enhanced the activity of ENaC in single channel patch-clamp experiments, an effect that was absent in cells transfected with a dominant negative P2X₄receptor construct, indicating that activation of P2X₄channels stimulates ENaC activity in these cells. The effect of meSATP on ENaC activity was reduced after chelation of basolateral Ca²⁺ with EGTA or inhibition of phosphatidylinositol 3-kinase with LY-294002. Overall, our results show that ENaC is stimulated by P2X₄receptor activation and that the stimulation is dependent on increases in intracellular Ca²⁺ and phosphatidylinositol 3-kinase activation.

Indexed as

AnimalsCalciumCell LineEpithelial Sodium ChannelsKidney Tubules, CollectingPhosphatidylinositol 3-KinasesReceptors, Purinergic P2X4XenopusCalciumEpithelial Sodium ChannelsPhosphatidylinositol 3-KinasesReceptors, Purinergic P2X4collecting ductintracellular calciumphosphatidylinositol 3-kinaseprincipal cellpurinergic receptor

Identifiers

PMID25100278
PMCPMC4187045
OpenAlexW2316499474

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.