Evidence map›Paper›PMID 39450718›Full record

ArticleJournal of the American Heart Association2024

Piezo1-Mediated Mechanotransduction Contributes to Disturbed Flow-Induced Atherosclerotic Endothelial Inflammation.

Yining Lan, Jing Lu, Shaohan Zhang, Chunxiao Jie, Chunyong Chen, Chao Xiao, Chao Qin, Daobin Cheng

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
–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

55 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  5. Article
  6. Review
  7. Nanomaterials-Based Immunotherapy for Atherosclerosis.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Review
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  9. Article
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  11. Article
  12. Article
  13. Article
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  15. Article
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  19. Mechanobiology of the Hippo-YAP Signaling Network.Cold Spring Harbor perspectives in biology · 2026
    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

8 authors.

Yining LanDepartment of Neurology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID 0009-0003-4340-956X
Jing LuDepartment of Neurology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID 0009-0007-2414-493X
Shaohan ZhangThe Second Affiliated Hospital of Qiqihar Medical College Qiqihar Heilongjiang China.ORCID 0009-0008-2059-587X
Chunxiao JieDepartment of Neurology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID 0009-0009-7442-5670
Chunyong ChenDepartment of Neurology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID 0000-0003-2157-3871
Chao XiaoDepartment of Neurology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID 0000-0003-1781-9680
Chao QinDepartment of Neurology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID 0000-0002-9965-2142
Daobin ChengDepartment of Neurology The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China.ORCID 0000-0003-0678-9543

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDisturbed flow generates oscillatory shear stress (OSS), which in turn leads to endothelial inflammation and atherosclerosis. Piezo1, a biomechanical force sensor, plays a crucial role in the cardiovascular system. However, the specific role of Piezo1 in atherosclerosis remains to be fully elucidated. METHODS AND

resultsWe detected the expression of Piezo1 in atherosclerotic mice and endothelial cells from regions with disturbed blood flow. The pharmacological inhibitor Piezo1 inhibitor (GsMTx4) was used to evaluate the impact of Piezo1 on plaque progression and endothelial inflammation. We examined Piezo1's direct response to OSS in vitro and its effects on endothelial inflammation. Furthermore, mechanistic studies were conducted to explore the potential molecular cascade through which Piezo1 mediates endothelial inflammation in response to OSS. Our findings revealed the upregulation of Piezo1 in apoE-/- (apolipoprotein E) atherosclerotic mice, which is associated with disturbed flow. Treatment with GsMTx4 not only delayed plaque progression but also mitigated endothelial inflammation in both chronic and disturbed flow-induced atherosclerosis. Piezo1 was shown to facilitate calcium ions (Ca

conclusionsOur study highlights the key role of Piezo1 in atherosclerotic endothelial inflammation, proposing the Piezo1-Ca

Indexed as

AtherosclerosisIon ChannelsMechanotransduction, CellularAnimalsCalcium SignalingCells, CulturedDisease Models, AnimalEndothelial CellsFocal Adhesion Kinase 1HumansInflammationIntercellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMice, Knockout, ApoEFocal Adhesion Kinase 1Intercellular Signaling Peptides and ProteinsIon ChannelsMTx4 protein, Grammostola spatulataPIEZO1 protein, humanPiezo1 protein, mousePtk2 protein, mouseSpider VenomsYap1 protein, mouseYAP-Signaling Proteinsatherosclerosisendothelial cellsinflammationPiezo1shear stress

Identifiers

PMID39450718
PMCPMC11935715

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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.