Evidence map›Paper›PMID 25736794›Full record

ArticleInvestigative ophthalmology & visual science2015

TRP Channels Localize to Subdomains of the Apical Plasma Membrane in Human Fetal Retinal Pigment Epithelium.

Peter Y Zhao, Geliang Gan, Shaomin Peng, Shao-Bin Wang, Bo Chen, Ron A Adelman, Lawrence J Rizzolo

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. The odyssey of the TR(i)P journey to the cellular membrane.Frontiers in cell and developmental biology · 2024
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Mutation of the TRPM3 cation channel underlies progressive cataract development and lens calcification associated with pro-fibrotic and immune cell responses.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  11. Review
  12. Review
  13. Review
  14. The Impact of miRNAs in Health and Disease of Retinal Pigment Epithelium.Frontiers in cell and developmental biology · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Cerebrospinal Fluid-Contacting Neurons Sense pH Changes and Motion in the Hypothalamus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    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

7 authors at 1 institution in 2 countries.

Peter Y ZhaoDepartment of Surgery, Yale University, New Haven, Connecticut, United States.
Geliang GanDepartment of Surgery, Yale University, New Haven, Connecticut, United States.
Shaomin PengDepartment of Surgery, Yale University, New Haven, Connecticut, United States.
Shao-Bin WangDepartment of Surgery, Yale University, New Haven, Connecticut, United States Department of Ophthalmology & Visual Science, Yale University, New Haven, Connecticut, United States.
Bo ChenDepartment of Ophthalmology & Visual Science, Yale University, New Haven, Connecticut, United States.
Ron A AdelmanDepartment of Ophthalmology & Visual Science, Yale University, New Haven, Connecticut, United States.
Lawrence J RizzoloDepartment of Surgery, Yale University, New Haven, Connecticut, United States Department of Ophthalmology & Visual Science, Yale University, New Haven, Connecticut, United States.
Yale University · US

Funding

Yale University Clinical and Translational Science Award ProgramUL1TR000142 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$31.8M
HDAC4-mediated Photoreceptor Protection in Retinal DegenerationR01EY021502 · NEI · YALE UNIVERSITY · PI CHEN, BO · 2012 to 2016
$2.0M
Regeneration of rod photoreceptors from Muller glial cells in adult mouse retinaR01EY024986 · NEI · YALE UNIVERSITY · PI CHEN, BO · 2016 to 2019
$1.6M
Yale University Clinical and Translational Science Award ProgramTL1TR000141 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$720k
NCATS NIH HHS CTSA-TL1 TR000141NCATS NIH HHS TL1 TR000141NCATS NIH HHS UL1 TR000142NEI NIH HHS R01 EY021502NEI NIH HHS R01 EY024986
6 · The paper itself

Abstract

purposeCalcium regulates many functions of the RPE. Its concentration in the subretinal space and RPE cytoplasm is closely regulated. Transient receptor potential (TRP) channels are a superfamily of ion channels that are moderately calcium-selective. This study investigates the subcellular localization and potential functions of TRP channels in a first-passage culture model of human fetal RPE (hfRPE).

methodsThe RPE isolated from 15- to 16-week gestation fetuses were maintained in serum-free media. Cultures were treated with barium chloride (BaCl2) in the absence and presence of TRP channel inhibitors and monitored by the transepithelial electrical resistance (TER). The expression of TRP channels was determined using quantitative RT-PCR, immunoblotting, and immunofluorescence confocal microscopy.

resultsBarium chloride substantially decreased TER and disrupted cell-cell contacts when added to the apical surface of RPE, but not when added to the basolateral surface. The effect could be partially blocked by the general TRP inhibitor, lanthanum chloride (LaCl3, ~75%), or an inhibitor of calpain (~25%). Family member-specific inhibitors, ML204 (TRPC4) and HC-067047 (TRPV4), had no effect on basal channel activity. Expression of TRPC4, TRPM1, TRPM3, TRPM7, and TRPV4 was detected by RT-PCR and immunoblotting. The TRPM3 localized to the base of the primary cilium, and TRPC4 and TRPM3 localized to apical tight junctions. The TRPV4 localized to apical microvilli in a small subset of cells.

conclusionsThe TRP channels localized to subdomains of the apical membrane, and BaCl2 was only able to dissociate tight junctions when presented to the apical membrane. The data suggest a potential role for TRP channels as sensors of [Ca(2+)] in the subretinal space.

Indexed as

Gene Expression RegulationBiological TransportCell MembraneCells, CulturedFetusHumansImmunoblottingImmunohistochemistryMembrane PotentialsMicroscopy, ConfocalReal-Time Polymerase Chain ReactionRetinal Pigment EpitheliumRNATight JunctionsTransient Receptor Potential ChannelsRNATransient Receptor Potential Channelsretinal pigment epitheliumsubretinal spacetight junctionTRP channels

Identifiers

PMID25736794
PMCPMC4364639
OpenAlexW2016889583

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.