Evidence map›Paper›PMID 25589752›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Agonist-dependent modulation of cell surface expression of the cold receptor TRPM8.

Carlos A Toro, Stephanie Eger, Luis Veliz, Pamela Sotelo-Hitschfeld, Deny Cabezas, Maite A Castro, Katharina Zimmermann, Sebastian Brauchi

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
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  5. Constitutive Phosphorylation as a Key Regulator of TRPM8 Channel Function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  6. Article
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  9. The Immunosuppressant Macrolide Tacrolimus Activates Cold-Sensing TRPM8 Channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  10. Article
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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.

Carlos A ToroInstituto de Fisiología, Facultad de Medicina, Escuela de Graduados, Facultad de Ciencias, Universidad Austral de Chile, Valdivia, Chile.
Stephanie EgerKlinik für Anästhesiologie, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany, and Institut für Physiologie und Pathophysiologie, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.
Luis VelizInstituto de Fisiología, Facultad de Medicina.
Pamela Sotelo-HitschfeldInstituto de Fisiología, Facultad de Medicina, Escuela de Graduados, Facultad de Ciencias, Universidad Austral de Chile, Valdivia, Chile.
Deny CabezasInstituto de Fisiología, Facultad de Medicina.
Maite A CastroInstituto de Bioquimica y Microbiologia, and.
Katharina ZimmermannKlinik für Anästhesiologie, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany, and Institut für Physiologie und Pathophysiologie, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany sbrauchi@uach.cl katharina.zimmermann@fau.de.
Sebastian BrauchiInstituto de Fisiología, Facultad de Medicina, sbrauchi@uach.cl katharina.zimmermann@fau.de.ORCID http://orcid.org/0000-0002-8494-9912

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spatial and temporal distribution of receptors constitutes an important mechanism for controlling the magnitude of cellular responses. Several members of the transient receptor potential (TRP) ion channel family can regulate their function by modulating their expression at the plasma membrane (PM) through rapid vesicular translocation and fusion. The mechanisms underlying this regulation are not completely understood, and the contribution of vesicular trafficking to physiological function is unknown. TRPM8 receptors are expressed in mammalian peripheral sensory neurons and are essential for the detection of cold temperatures. Previously, we showed that TRPM8-containing vesicles are segregated into three main pools, immobile at the PM, simple diffusive and corralled-hopping. Here, we show that channel expression at the PM is modulated by TRPM8 agonists in F11 and HEK293T cells. Our results support a model in which the activation of TRPM8 channels, located at the PM, induces a short-lived recruitment of a TRPM8-containing vesicular pool to the cell surface causing a transitory increase in the number of functional channels, affecting intrinsic properties of cold receptor responses. We further demonstrate the requirement of intact vesicular trafficking to support sustained cold responses in the skin of mice.

Indexed as

AnimalsBotulinum Toxins, Type ACell Line, TumorCell MembraneHEK293 CellsHumansMiceMice, Inbred C57BLNeurotoxinsProtein TransportRatsSensory Receptor CellsTRPM Cation ChannelsBotulinum Toxins, Type ANeurotoxinsTrpm8 protein, ratTRPM Cation ChannelsBotulinum neurotoxin Type A (BoNTA)colddiffusionperipheral sensory neuronsskin nerve preparationvesicle

Identifiers

PMID25589752
PMCPMC6605369

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.