Evidence map›Paper›PMID 22204737›Full record

ArticleCell calcium2012

Hypotonicity-induced TRPV4 function in renal collecting duct cells: modulation by progressive cross-talk with Ca2+-activated K+ channels.

Min Jin, Jonathan Berrout, Ling Chen, Roger G O'Neil

Open access · greenAbstract read
In one paragraph

Article in Cell calcium, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Ablation of Endothelial TRPV4 Channels Alters the Dynamic CaInternational journal of molecular sciences · 2020
    Article
  3. Article
  4. Article
  5. Caveolae facilitate TRPV4-mediated CaAmerican journal of physiology. Renal physiology · 2018
    Article
  6. TRPV4 channels contribute to renal myogenic autoregulation in neonatal pigs.American journal of physiology. Renal physiology · 2017
    Article
  7. Dynamic coupling between TRPV4 and CaAmerican journal of physiology. Renal physiology · 2017
    Article
  8. Article
  9. Calcium-permeable ion channels in the kidney.American journal of physiology. Renal physiology · 2016
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. TRPV4 activation in mouse submandibular gland modulates Ca2+ influx and salivation.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Article
  19. 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

4 authors at 1 institution in 1 country.

Min JinDept. of Integrative Biology and Pharmacology, The University of Texas Health Science Center, Houston, TX 77030, USA.
Jonathan Berrout
Ling Chen
Roger G O'Neil
The University of Texas Health Science Center at Houston · US

Funding

Role of TRP Channels on Collecting Duct Calcium DynamicsR01DK070950 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI O'NEIL, ROGER GORDON · 2005 to 2009
$1.4M
RNA Aptamers Selective for TPRV ChannelsR21DE018522 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI O'NEIL, ROGER GORDON · 2008 to 2009
$412k
NIDCR NIH HHS R21 DE018522NIDDK NIH HHS R01 DK070950
6 · The paper itself

Abstract

The mouse cortical collecting duct (CCD) M-1 cells were grown to confluency on coverslips to assess the interaction between TRPV4 and Ca(2+)-activated K(+) channels. Immunocytochemistry demonstrated strong expression of TRPV4, along with the CCD marker, aquaporin-2, and the Ca(2+)-activated K(+) channels, the small conductance SK3 (K(Ca)2.3) channel and large conductance BKα channel (K(Ca)1.1). TRPV4 overexpression studies demonstrated little physical dependency of the K(+) channels on TRPV4. However, activation of TRPV4 by hypotonic swelling (or GSK1016790A, a selective agonist) or inhibition by the selective antagonist, HC-067047, demonstrated a strong dependency of SK3 and BK-α activation on TRPV4-mediated Ca(2+) influx. Selective inhibition of BK-α channel (Iberiotoxin) or SK3 channel (apamin), thereby depolarizing the cells, further revealed a significant dependency of TRPV4-mediated Ca(2+) influx on activation of both K(+) channels. It is concluded that a synergistic cross-talk exists between the TRPV4 channel and SK3 and BK-α channels to provide a tight functional regulation between the channel groups. This cross-talk may be progressive in nature where the initial TRPV4-mediated Ca(2+) influx would first activate the highly Ca(2+)-sensitive SK3 channel which, in turn, would lead to enhanced Ca(2+) influx and activation of the less Ca(2+)-sensitive BK channel.

Indexed as

AnimalsApaminAquaporin 2CalciumCell LineGene Expression RegulationKidney Tubules, CollectingLarge-Conductance Calcium-Activated Potassium ChannelsLeucineMicePeptidesSmall-Conductance Calcium-Activated Potassium ChannelsSulfonamidesTRPV Cation ChannelsApaminAqp2 protein, mouseAquaporin 2CalciumiberiotoxinKcnn3 protein, mouseLarge-Conductance Calcium-Activated Potassium ChannelsLeucineN-(1-((4-(2-(((2,4-dichlorophenyl)sulfonyl)amino)-3-hydroxypropanoyl)-1-piperazinyl)carbonyl)-3-methylbutyl)-1-benzothiophene-2-carboxamidePeptidesSmall-Conductance Calcium-Activated Potassium ChannelsSulfonamidesTrpv4 protein, mouseTRPV Cation Channels

Identifiers

PMID22204737
PMCPMC3279617
OpenAlexW2028654985

What OpenQuestion holds

Textmetadata
LicenceTDM
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.