Evidence map›Paper›PMID 31820013›Full record

ArticleThe Journal of membrane biology2020

Transient Receptor Potential Ankyrin 1 Contributes to Lysophosphatidylcholine-Induced Intracellular Calcium Regulation and THP-1-Derived Macrophage Activation.

Chao Tian, Rongqi Huang, Feng Tang, Zuoxian Lin, Na Cheng, Xiaobo Han, Shuai Li, Peng Zhou, Sihao Deng, Hualin Huang and 3 more

Abstract read
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In one paragraph

Article in The Journal of membrane biology, 2020. 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
1.5field-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, 27 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. Article
  9. TRPA1 Expression and Pathophysiology in Immune Cells.International journal of molecular sciences · 2021
    Review
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  11. Review
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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 4 institutions in 1 country.

Chao TianSchool of Life Sciences, University of Science and Technology of China, Hefei, Anhui, China.
Rongqi HuangKey Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, #190 Kai-Yuan Road, Guangzhou Science Park, Guangzhou, 510530, China.
Feng TangKey Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, #190 Kai-Yuan Road, Guangzhou Science Park, Guangzhou, 510530, China.
Zuoxian LinKey Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, #190 Kai-Yuan Road, Guangzhou Science Park, Guangzhou, 510530, China.
Na ChengKey Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, #190 Kai-Yuan Road, Guangzhou Science Park, Guangzhou, 510530, China.
Xiaobo HanKey Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, #190 Kai-Yuan Road, Guangzhou Science Park, Guangzhou, 510530, China.
Shuai LiKey Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, #190 Kai-Yuan Road, Guangzhou Science Park, Guangzhou, 510530, China.
Peng ZhouDepartment of Anatomy and Neurobiology, School of Basic Medical Sciences, Central South University, Changsha, Hunan, China.
Sihao DengDepartment of Anatomy and Neurobiology, School of Basic Medical Sciences, Central South University, Changsha, Hunan, China.
Hualin HuangKey Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, #190 Kai-Yuan Road, Guangzhou Science Park, Guangzhou, 510530, China.
Huifang ZhaoSchool of Life Sciences, University of Science and Technology of China, Hefei, Anhui, China.
Junjie XuGuangzhou JYK Biotechnology Company Limited, Guangzhou, Guangdong, China.
Zhiyuan LiSchool of Life Sciences, University of Science and Technology of China, Hefei, Anhui, China. li_zhiyuan@gibh.ac.cn.
Guangzhou Regenerative Medicine and Health Guangdong Laboratory · CNGuangzhou Institutes of Biomedicine and Health · CNCentral South University · CNUniversity of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lysophosphatidylcholine (LPC) is a major atherogenic lipid that stimulates an increase in mitochondrial reactive oxygen species (mtROS) and the release of cytokines under inflammasome activation. However, the potential receptors of LPC in macrophages are poorly understood. Members of the transient receptor potential (TRP) channel superfamily, which is crucially involved in transducing environmental irritant stimuli into nociceptor activity, are potential receptors of LPC. In this study, we investigated whether LPC can induce the activation of transient receptor potential ankyrin 1 (TRPA1), a member of the TRP superfamily. The functional expression of TRPA1 was first detected by quantitative real-time polymerase chain reaction (qRT-PCR), western blotting and calcium imaging in human acute monocytic leukemia cell line (THP-1)-derived macrophages. The mechanism by which LPC induces the activation of macrophages through TRPA1 was verified by cytoplasmic and mitochondrial calcium imaging, mtROS detection, a JC-1 assay, enzyme-linked immunosorbent assay, the CCK-8 assay and the lactate dehydrogenase (LDH) cytotoxic assay. LPC induced the activation of THP-1-derived macrophages via calcium influx, and this activation was suppressed by potent and selective inhibitors of TRPA1. These results indicated that TRPA1 can mediate mtROS generation, mitochondrial membrane depolarization, the secretion of IL-1β and cytotoxicity through cellular and mitochondrial Ca

Indexed as

BiomarkersCalciumCell LineCells, CulturedHumansIntracellular SpaceLysophosphatidylcholinesMacrophage ActivationMacrophagesMembrane Potential, MitochondrialMitochondriaMolecular ImagingReactive Oxygen SpeciesTRPA1 Cation ChannelBiomarkersCalciumLysophosphatidylcholinesReactive Oxygen SpeciesTRPA1 Cation ChannelCalciumLPCMacrophageMitochondriaReactive oxygen speciesTRPA1

Identifiers

PMID31820013
OpenAlexW2992436556

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.