Evidence map›Paper›PMID 29038158›Full record

ArticleMolecular pharmacology2017

Activation of Human Transient Receptor Potential Melastatin-8 (TRPM8) by Calcium-Rich Particulate Materials and Effects on Human Lung Cells.

John G Lamb, Erin G Romero, Zhenyu Lu, Seychelle K Marcus, Hannah C Peterson, John M Veranth, Cassandra E Deering-Rice, Christopher A Reilly

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. TRP Channels as Cellular Targets of Particulate Matter.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Molecular pharmacology · 2019
    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

8 authors at 1 institution in 1 country.

John G LambDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah.
Erin G RomeroDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah.
Zhenyu LuDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah.
Seychelle K MarcusDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah.
Hannah C PetersonDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah.
John M VeranthDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah.
Cassandra E Deering-RiceDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah.
Christopher A ReillyDepartment of Pharmacology and Toxicology, Center for Human Toxicology, University of Utah, Salt Lake City, Utah Chris.Reilly@pharm.utah.edu.
University of Utah · US

Funding

TRP Channels and Air PollutionR01ES017431 · NIEHS · UNIVERSITY OF UTAH · PI REILLY, CHRISTOPHER A · 2009 to 2024
$5.3M
NIEHS NIH HHS R01 ES017431
6 · The paper itself

Abstract

To better understand how adverse health effects are caused by exposure to particulate materials, and to develop preventative measures, it is important to identify the properties of particles and molecular targets that link exposure with specific biologic outcomes. Coal fly ash (CFA) is a by-product of coal combustion that can affect human health. We report that human transient receptor potential melastatin-8 (TRPM8) and an N-terminally truncated TRPM8 variant (TRPM8-Δ801) are activated by CFA and calcium-rich nanoparticles and/or soluble salts within CFA. TRPM8 activation by CFA was potentiated by cold temperature involving the phosphatidylinositol 4,5-bisphosphate binding residue (L1008), but was independent of the icilin and menthol binding site residue Y745 and, essentially, the N-terminal amino acids 1-800. CFA, calcium nanoparticles, and calcium salts also activated transient receptor potential vanilloid-1 (TRPV1) and transient receptor potential ankyrin-1 (TRPA1), but not TRPV4. CFA treatment induced CXCL1 and interleukin-8 mRNA in BEAS-2B and primary human bronchial epithelial cells through activation of both TRPM8 and TRPV1. However, neither mouse nor rat TRPM8 was activated by these materials, and

Indexed as

AnimalsBronchiCalciumCalcium CompoundsCalcium PhosphatesCell LineCoal AshCytokinesHumansInflammationMice, Inbred C57BLMice, KnockoutOxidesParticulate MatterRatsRespiratory MucosaCalciumCalcium Compoundscalcium phosphateCalcium PhosphatesCoal AshCytokineslimeOxidesParticulate MatterTRPM8 protein, humanTRPM8 protein, mouseTrpm8 protein, ratTRPM Cation Channels

Identifiers

PMID29038158
PMCPMC5695664
OpenAlexW2766454174

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.