Evidence map›Paper›PMID 29447005›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2018

Human ASIC1a mediates stronger acid-induced responses as compared with mouse ASIC1a.

Yuanyuan Xu, Yu-Qing Jiang, Ce Li, Mindi He, W George Rusyniak, Naga Annamdevula, Juan Ochoa, Silas J Leavesley, Jiangping Xu, Thomas C Rich and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Inhibition of ASIC1a reduces ferroptosis in rheumatoid arthritis articular chondrocytes via the p53/NRF2/SLC7A11 pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. RNA-Seq analysis of knocking out the neuroprotective proton-sensitive GPR68 on basal and acute ischemia-induced transcriptome changes and signaling in mouse brain.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  12. Article
  13. Signaling Pathways in Proton and Non-proton ASIC1a Activation.Frontiers in cellular neuroscience · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

12 authors at 4 institutions in 2 countries.

Yuanyuan XuDepartment of Physiology and Cell Biology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Yu-Qing JiangDepartment of Physiology and Cell Biology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Ce LiDepartment of Physiology and Cell Biology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Mindi HeDepartment of Physiology and Cell Biology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
W George RusyniakDepartment of Neurosurgery, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Naga AnnamdevulaDepartment of Pharmacology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Juan OchoaDepartment of Neurology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Silas J LeavesleyChemical and Biomolecular Engineering, College of Engineering, University of South Alabama, Mobile, Alabama, USA.
Jiangping XuDepartment of Neuropharmacology and Drug Discovery, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Thomas C RichDepartment of Pharmacology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Mike T LinDepartment of Physiology and Cell Biology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
Xiang-Ming ZhaDepartment of Physiology and Cell Biology, College of Medicine, University of South Alabama, Mobile, Alabama, USA.
University of South Alabama · USHuashan Hospital · CNSouthern Medical University · CNThird Hospital of Hebei Medical University · CN

Funding

T-type Calcium Channels and von Willebrand Factor ReleaseP01HL066299 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI ALVAREZ, DIEGO F. · 2001 to 2022
$34.6M
Neuroprotective role of OGR1 in brain ischemiaR01NS102495 · NINDS · UNIVERSITY OF SOUTH ALABAMA · PI ZHA, XIANGMING · 2017 to 2022
$1.8M
OGR1 as a novel mediator of acid signaling in the brainR21NS093522 · NINDS · UNIVERSITY OF SOUTH ALABAMA · PI ZHA, XIANGMING · 2015 to 2016
$406k
Request for a Spectral Confocal MicroscopeS10RR027535 · NCRR · UNIVERSITY OF SOUTH ALABAMA · PI RICH, THOMAS C · 2010 to 2010
$397k
Andor Revolution WD Confocal Imaging SystemS10OD020149 · OD · UNIVERSITY OF SOUTH ALABAMA · PI TAYLOR, MARK STEPHEN · 2015 to 2015
$395k
NCRR NIH HHS S10 RR027535NHLBI NIH HHS P01 HL066299NIH HHS S10 OD020149NINDS NIH HHS R01 NS102495NINDS NIH HHS R21 NS093522
6 · The paper itself

Abstract

Acid-sensing ion channels (ASICs) are the major proton receptor in the brain and a key mediator of acidosis-induced neuronal injuries in disease. Most of published data on ASIC function came from studies performed in mice, and relatively little is known about potential differences between human and mouse ASICs (hASIC and mASIC, respectively). This information is critical for us to better interpret the functional importance of ASICs in human disease. Here, we examined the expression of ASICs in acutely resected human cortical tissue. Compared with mouse cortex, human cortical tissue showed a similar ratio of ASIC1a:ASIC2a expression, had reduced ASIC2b level, and exhibited a higher membrane:total ratio of ASIC1a. We further investigated the mechanism for higher surface trafficking of hASIC1a in heterologous cells. A single amino acid at position 285 was critical for increased N-glycosylation and surface expression of hASIC1a. Consistent with the changes in trafficking and current, cells expressing hASIC1a or mASIC1a S285P mutant had a higher acid-activated calcium increase and exhibited worsened acidotoxicity. These data suggest that ASICs are likely to have a larger impact on acidosis-induced neuronal injuries in humans than mice, and this effect is, at least in part, a result of more efficient trafficking of hASIC1a.-Xu, Y., Jiang, Y.-Q., Li, C., He, M., Rusyniak, W. G., Annamdevula, N., Ochoa, J., Leavesley, S. J., Xu, J., Rich, T. C., Lin, M. T., Zha, X.-M. Human ASIC1a mediates stronger acid-induced responses as compared with mouse ASIC1a.

Indexed as

ProtonsAcid Sensing Ion ChannelsAction PotentialsAdolescentAdultAnimalsCalciumCerebral CortexCHO CellsCricetinaeCricetulusFemaleHumansIon Channel GatingMaleMiceAcid Sensing Ion ChannelsCalciumProtonsacidosiscalciumneuronal injurytrafficking

Identifiers

PMID29447005
PMCPMC5998965
OpenAlexW2792047193

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.