Evidence map›Paper›PMID 40643822›Full record

ArticleTissue engineering and regenerative medicine2025

SIRT4 Regulated by a Mechanosensor, PIEZO1 Shows a Protective Function to Suppress Ox-LDL Uptake in Endothelial Cells.

Vadym Kopych, Avelino Dos Santos Da Costa, Kwideok Park

Abstract read
In one paragraph

Article in Tissue engineering and regenerative medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

3 authors.

Vadym KopychCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.ORCID http://orcid.org/0009-0002-3021-2955
Avelino Dos Santos Da CostaCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.ORCID http://orcid.org/0000-0002-1787-9029
Kwideok ParkCenter for Biomaterials, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea. kpark@kist.re.kr.ORCID http://orcid.org/0000-0001-8519-8316

Funding

Ministry of Science and ICT, South Korea RS-2025-00516184
6 · The paper itself

Abstract

backgroundEndothelial cells (ECs) are key regulators of vascular function, adapting to mechanical forces, such as shear stress to maintain vascular homeostasis. Disruption of this adaptation, particularly in the regions of disturbed flow, contributes to endothelial dysfunction and the development of atherosclerosis later on.

methodsWe prepared a custom-designed PDMS-based flow chamber to apply controlled shear stress (2 or 7 dynes/cm

resultsWe demonstrated that the mechanosensitive ion channel PIEZO1, regulates SIRT4 expression in response to shear stress. Under atheroprotective shear stress (7 dyne/cm

conclusionCurrent findings suggest that the PIEZO1-SIRT4 axis may modulate endothelial responses to shear stress, offering a protective mechanism against Ox-LDL-induced dysfunction and pathology. Our study underscores the potential of SIRT4 as a therapeutic target to mitigate vascular disorders associated with oxidative stress and disturbed blood flow.

Indexed as

Human Umbilical Vein Endothelial CellsIon ChannelsLipoproteins, LDLMitochondrial ProteinsSirtuinsAtherosclerosisBlood CirculationCell LineGene Knockdown TechniquesHumansOxidation-ReductionOxidative StressStress, MechanicalIon ChannelsLipoproteins, LDLMitochondrial Proteinsoxidized low density lipoproteinPIEZO1 protein, humanSIRT4 protein, humanSirtuinsEndothelial cellsPIEZO1Shear stressSIRT4

Identifiers

PMID40643822
PMCPMC12476331

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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.