Evidence map›Paper›PMID 25503733›Full record

ReviewAmerican journal of physiology. Renal physiology2015

Deciphering physiological role of the mechanosensitive TRPV4 channel in the distal nephron.

M Mamenko, O Zaika, N Boukelmoune, R G O'Neil, O Pochynyuk

Abstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. TRPV4 expression in the renal tubule is necessary for maintaining whole body KAmerican journal of physiology. Renal physiology · 2023
    Article
  5. Following Ussing's legacy: from amphibian models to mammalian kidney and brain.American journal of physiology. Cell physiology · 2022
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Roles of TRPV4 and piezo channels in stretch-evoked CaExperimental biology and medicine (Maywood, N.J.) · 2020
    Article
  15. TRPV4 deletion protects against hypokalemia during systemic KAmerican journal of physiology. Renal physiology · 2019
    Article
  16. TRP Channels as Drug Targets to Relieve Itch.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
  17. Deficient transient receptor potential vanilloid type 4 function contributes to compromised [CaFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

M MamenkoDepartment of Integrative Biology and Pharmacology, University of Texas Health Science Center, Houston, Texas.
O ZaikaDepartment of Integrative Biology and Pharmacology, University of Texas Health Science Center, Houston, Texas.
N BoukelmouneDepartment of Integrative Biology and Pharmacology, University of Texas Health Science Center, Houston, Texas.
R G O'NeilDepartment of Integrative Biology and Pharmacology, University of Texas Health Science Center, Houston, Texas.
O PochynyukDepartment of Integrative Biology and Pharmacology, University of Texas Health Science Center, Houston, Texas Oleh.M.Pochynyuk@uth.tmc.edu.
The University of Texas Health Science Center at Houston · US

Funding

Aldosterone-independent regulation of ENaC by systemic saltR01DK095029 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI POCHYNYUK, OLEH · 2012 to 2016
$1.6M
NIDDK NIH HHS DK095029NIDDK NIH HHS R01 DK095029
6 · The paper itself

Abstract

Long-standing experimental evidence suggests that epithelial cells in the renal tubule are able to sense osmotic and pressure gradients caused by alterations in ultrafiltrate flow by elevating intracellular Ca(2+) concentration. These responses are viewed as critical regulators of a variety of processes ranging from transport of water and solutes to cellular growth and differentiation. A loss in the ability to sense mechanical stimuli has been implicated in numerous pathologies associated with systemic imbalance of electrolytes and to the development of polycystic kidney disease. The molecular mechanisms conferring mechanosensitive properties to epithelial tubular cells involve activation of transient receptor potential (TRP) channels, such as TRPV4, allowing direct Ca(2+) influx to increase intracellular Ca(2+) concentration. In this review, we critically analyze the current evidence about signaling determinants of TRPV4 activation by luminal flow in the distal nephron and discuss how dysfunction of this mechanism contributes to the progression of polycystic kidney disease. We also review the physiological relevance of TRPV4-based mechanosensitivity in controlling flow-dependent K(+) secretion in the distal renal tubule.

Indexed as

Mechanotransduction, CellularAnimalsCalciumEpithelial CellsHomeostasisHumansHyperkalemiaNephronsOsmotic PressurePolycystic Kidney DiseasesPotassiumPressureTRPV Cation ChannelsCalciumPotassiumTRPV4 protein, humanTRPV Cation Channelsflow sensitivitymechanosensitive intracellular Ca2+ concentration signalingpolycystic kidney diseaserenal potassium excretiontransient receptor potential cation channel subfamily V member 4

Identifiers

PMID25503733
PMCPMC4329491
OpenAlexW2093045380

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.