Evidence map›Paper›PMID 30074209›Full record

ArticleCurrent medical science2018

Identification and Function of Acid-sensing Ion Channels in RAW 264.7 Macrophage Cells.

Lan Ni, Peng Fang, Zhuang-Li Hu, Hai-Yun Zhou, Jian-Guo Chen, Fang Wang, You Jin

Abstract read
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In one paragraph

Article in Current medical science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 32% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Macrophages sense and follow physiologically relevant KCell communication and signaling : CCS · 2026
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  8. Review
  9. Epithelial sodium channels in macrophage migration and polarization: role of proinflammatory cytokines TNFα and IFNγ.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  10. Review
  11. Evidence for role of acid-sensing ion channel 1a in chronic rhinosinusitis with nasal polyps.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2021
    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

7 authors at 2 institutions in 1 country.

Lan NiDepartment of Pharmacology, Huazhong University of Science and Technology, Wuhan, 430030, China.
Peng FangDepartment of Pharmacology, Huazhong University of Science and Technology, Wuhan, 430030, China.
Zhuang-Li HuDepartment of Pharmacology, Huazhong University of Science and Technology, Wuhan, 430030, China.
Hai-Yun ZhouDepartment of Pharmacology, Huazhong University of Science and Technology, Wuhan, 430030, China.
Jian-Guo ChenDepartment of Pharmacology, Huazhong University of Science and Technology, Wuhan, 430030, China.
Fang WangDepartment of Pharmacology, Huazhong University of Science and Technology, Wuhan, 430030, China.
You JinDepartment of Pharmacology, Huazhong University of Science and Technology, Wuhan, 430030, China. 158735589@qq.com.
Huazhong University of Science and Technology · CNHuazhong Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of acid-sensing ion channels (ASICs) plays an important role in neuroinflammation. Macrophage recruitment to the sites of inflammation is an essential step in host defense. ASIC1 and ASIC3 have been reported to mediate the endocytosis and maturation of bone marrow derived macrophages. However, the expression and inflammation-related functions of ASICs in RAW 264.7 cells, another common macrophage, are still elusive. In the present study, we first demonstrated the presence of ASIC1, ASIC2a and ASIC3 in RAW 264.7 macrophage cell line by using reverse transcriptase polymerase chain reaction (RT-PCR), Western blotting and immunofluorescence experiments. The non-specific ASICs inhibitor amiloride and specific homomeric ASICla blocker PcTxl reduced the production of iNOS and COX-2 by LPS-induced activating RAW 264.7 cells. Furthermore, not only amiloride but also PcTxl inhibited the migration and LPS-induced apoptosis of RAW 264.7 cells. Taken together, our findings suggest that ASICs promote the inflammatory response and apoptosis of RAW 264.7 cells, and ASICs may serve as a potential novel target for immunological disease therapy.

Indexed as

Acid Sensing Ion ChannelsAnimalsApoptosisCell MovementInflammationLipopolysaccharidesMacrophagesMiceRAW 264.7 CellsAcid Sensing Ion ChannelsLipopolysaccharidesacid-sensing ion channels (ASICs)apoptosisinflammationmigrationRAW 264.7 cells

Identifiers

PMID30074209
OpenAlexW2809357685

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.