Evidence map›Paper›PMID 26656285›Full record

ArticleScientific reports2015

A dual role of transient receptor potential melastatin 2 channel in cytotoxicity induced by silica nanoparticles.

Peilin Yu, Jin Li, Jialin Jiang, Zunquan Zhao, Zhaoyuan Hui, Jun Zhang, Yifan Zheng, Daishun Ling, Lie Wang, Lin-Hua Jiang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. TRP Channels as Cellular Targets of Particulate Matter.International journal of molecular sciences · 2021
    Review
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  7. 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

13 authors at 2 institutions in 2 countries.

Peilin YuDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Jin LiDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Jialin JiangDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Zunquan ZhaoDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Zhaoyuan HuiInstitute of Immunology, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, P. R. China.
Jun ZhangDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Yifan ZhengDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Daishun LingCollege of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Lie WangInstitute of Immunology, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, P. R. China.
Lin-Hua JiangSchool of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.
Jianhong LuoDepartment of Neurobiology, Key Laboratory of Medical Neurobiology of the Ministry of Health of China, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, P. R. China.
Xinqiang ZhuDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang 310058, P. R. China.
Wei YangDepartment of Neurobiology, Key Laboratory of Medical Neurobiology of the Ministry of Health of China, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, P. R. China.
Zhejiang University · CNUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Silica nanoparticles (NPs) have remarkable applications. However, accumulating evidence suggests NPs can cause cellular toxicity by inducing ROS production and increasing intracellular Ca(2+) ([Ca(2+)]i), but the underlying molecular mechanism is largely unknown. Transient receptor potential melastatin 2 (TRPM2) channel is known to be a cellular redox potential sensor that provides an important pathway for increasing the [Ca(2+)]i under oxidative stress. In this study, we examined the role of TRPM2 channel in silica NPs-induced oxidative stress and cell death. By quantitation of cell viability, ROS production, [Ca(2+)]i, and protein identification, we showed that TRPM2 channel is required for ROS production and Ca(2+) increase induced by silica NPs through regulating NADPH oxidase activity in HEK293 cells. Strikingly, HEK293 cells expressing low levels of TRPM2 were more susceptible to silica NPs than those expressing high levels of TRPM2. Macrophages from young mice showed significantly lower TRPM2 expression than those from senescent mice and had significantly lower viability after silica NPs exposure than those from senescent ones. Taken together, these findings demonstrate for the first time that TRPM2 channel acts as an oxidative stress sensor that plays a dual role in silica NPs-induced cytotoxicity by differentially regulating the NADPH oxidase activity and ROS generation.

Indexed as

Age FactorsAnimalsCalciumCells, CulturedCell SurvivalHEK293 CellsHumansIntracellular SpaceIon Channel GatingMacrophagesMaleMembrane PotentialsMice, Inbred C57BLMicroscopy, Electron, TransmissionNADPH OxidasesNanoparticlesCalciumNADPH OxidasesReactive Oxygen SpeciesSilicon DioxideTRPM2 protein, humanTRPM Cation Channels

Identifiers

PMID26656285
PMCPMC4676061
OpenAlexW2419292143

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.