Evidence map›Paper›PMID 20580783›Full record

ArticleNeuroscience2010

The development of peripheral cold neural circuits based on TRPM8 expression.

Y Takashima, L Ma, D D McKemy

Abstract read
In one paragraph

Article in Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. The development of somatosensory neurons: Insights into pain and itch.Current topics in developmental biology · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. The neural circuits of thermal perception.Current opinion in neurobiology · 2018
    Review
  18. TrpM8-mediated somatosensation in mouse neocortex.The Journal of comparative neurology · 2018
    Article
  19. Article
  20. Molecular basis of peripheral innocuous cold sensitivity.Handbook of clinical neurology · 2018
    Review
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

3 authors at 1 institution in 1 country.

Y TakashimaNeuroscience Graduate Program, University of Southern California, Los Angeles, CA 90089, USA.
L Ma
D D McKemy
University of Southern California · US

Funding

Molecular Mechanisms of Axon Branching in Synaptic DevelopmentR01NS062047 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MA, LE · 2009 to 2018
$3.4M
Neurobiological Basis for Cold TransductionR01NS054069 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MCKEMY, DAVID D · 2007 to 2010
$1.5M
NINDS NIH HHS NS054069NINDS NIH HHS R01 NS054069NINDS NIH HHS R01 NS062047
6 · The paper itself

Abstract

Afferent nerve fibers of the somatosensory system are a molecularly diverse cell population that detects a varied range of environmental stimuli, converting these external cues ultimately into a sensory percept. Afferents mediating detection of thermal stimuli express a repertoire of temperature sensitive ion channels of the TRP family which endow these nerves with the ability to respond to the breadth of temperatures in the environment. The cold and menthol receptor TRPM8 is responsible for detection of cold and, unlike other thermosensors, detects both innocuous and noxious temperatures. How this single molecule can perform such diverse functions is currently unknown, but expression analyses in adult tissues shows that TRPM8 neurons are a molecularly diverse population and it is likely that this diversity underlies differential functionality. To determine how this phenotype is established, we examined the developmental time course of TRPM8 expression using a mouse transgenic line in which GFP expression is driven by the TRPM8 transcriptional promoter (Trpm8(GFP)). We find that Trpm8(GFP) expression begins prior to embryonic day 15.5 (E15.5) after which expression reaches levels observed in adult neurons. By E18.5, central axons of Trpm8(GFP) neurons reach the spinal cord dorsal horn, but anatomical localization and in vivo measurements of neural activity suggest that fully functional cold circuits are not established until after the first postnatal week. Additionally, Trpm8(GFP) neurons undergo a transition in neurochemical phenotype, ultimately reaching adult expression of markers such TRPV1, CGRP, peripherin, and NF200 by postnatal day 14. Thus, based on immunochemical, anatomical and functional criteria, active cold neural circuits are fully established by the second week postnatal, thereby suggesting that important extrinsic or intrinsic mechanisms are active prior to this developmental stage.

Indexed as

Cold TemperatureAfferent PathwaysAnimalsAxonsEmbryo, MammalianIn Vitro TechniquesMiceMice, TransgenicPosterior Horn CellsReceptors, Nerve Growth FactorSpinal CordSynapsesTRPM Cation ChannelsReceptors, Nerve Growth FactorTRPM8 protein, mouseTRPM Cation Channels

Identifiers

PMID20580783
PMCPMC2904417
OpenAlexW1980360344

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.