Evidence map›Paper›PMID 41856078›Full record

ArticleThe journal of physiological sciences : JPS2026

Dynamic regulation of TASK-1 channels under cellular stress.

Yang Yu, John Curry, Sarah Tankersley, Keli Hu

Abstract read
In one paragraph

Article in The journal of physiological sciences : JPS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Yang YuDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.
John CurryDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.
Sarah TankersleyDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.
Keli HuDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA. Electronic address: hu.175@osu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TASK-1 channel is important for regulating membrane potential. However, its response to pathological conditions remains unknown. In this study, we investigated the effects of hypoxia on the recombinant TASK-1 channel localization at the surface of HEK293T cells. The hypoxic condition was induced via sodium cyanide (NaCN) treatment. Exposure to NaCN led to a significant decrease in TASK-1 levels at the cell surface. This reduction was blocked by pre-exposure to a selective protein kinase C (PKC) inhibitor bisindolylmaleimide. Additional experiments demonstrated that blocking dynamin function or depleting cellular cholesterol prevented TASK-1 from the reduction at the cell surface. Fluorescence microscopic analysis further showed a selective reduction in cell surface wild type TASK-1 under hypoxic conditions, while double-leucine mutant TASK-1 remained unchanged. These results reveal a novel mechanism by which TASK-1 channel localization is modulated by chemical hypoxia, highlighting the importance of PKC, dynamin, and cholesterol in regulating TASK-1 trafficking.

Indexed as

Nerve Tissue ProteinsPotassium Channels, Tandem Pore DomainStress, PhysiologicalCell HypoxiaCell MembraneCholesterolDynaminsHEK293 CellsHumansIndolesMaleimidesProtein Kinase CProtein TransportCholesterolDynaminsIndolesMaleimidesNerve Tissue ProteinsPotassium Channels, Tandem Pore Domainpotassium channel subfamily K member 3Protein Kinase CCellular stressDynaminProtein kinase CTASK-1

Identifiers

PMID41856078
PMCPMC13015633

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LicenceCC BY-NC-ND
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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.