Evidence map›Paper›PMID 36130017›Full record

ArticleScience translational medicine2022

Receptor-independent fluid-phase macropinocytosis promotes arterial foam cell formation and atherosclerosis.

Hui-Ping Lin, Bhupesh Singla, WonMo Ahn, Pushpankur Ghoshal, Maria Blahove, Mary Cherian-Shaw, Alex Chen, April Haller, David Y Hui, Kunzhe Dong and 9 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Myeloid Cell-Specific Deletion of LGR4 Suppresses Atherosclerotic Lesion Formation.Arteriosclerosis, thrombosis, and vascular biology · 2026
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  19. Regulatory roles of PIWI-interacting RNAs in cardiovascular disease.American journal of physiology. Heart and circulatory physiology · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 2 countries.

Hui-Ping LinVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-3136-9543
Bhupesh SinglaVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0003-2752-6849
WonMo AhnVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0001-9735-8022
Pushpankur GhoshalVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0003-0233-4701
Maria BlahoveVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-9022-7801
Mary Cherian-ShawVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-8079-6453
Alex ChenVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0001-5662-8188
April HallerCenter for Lipid and Arteriosclerosis Science, Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.ORCID 0000-0002-0560-3033
David Y HuiCenter for Lipid and Arteriosclerosis Science, Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.ORCID 0000-0001-7333-2151
Kunzhe DongDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0003-0039-9835
Jiliang ZhouDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-2375-4636
Joseph WhiteDepartment of Pathology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0003-0289-686X
Alexis M StranahanDepartment of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0003-0612-2837
Agnieszka JasztalJagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University, Bobrzynskiego 14, 30-348 Krakow, Poland.ORCID 0000-0002-5790-1059
Rudolf LucasVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0003-3805-8868
Brian K StansfieldVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-1105-8895
David FultonVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-1528-1517
Stefan ChlopickiJagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University, Bobrzynskiego 14, 30-348 Krakow, Poland.ORCID 0000-0002-2878-3858
Gábor CsányiVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-4429-3031
Augusta University · USJagiellonian University · PLUniversity of Cincinnati · US

Funding

Inflammation and retinopathy of prematurityR01EY029318 · NEI · AUGUSTA UNIVERSITY · PI STANSFIELD, BRIAN KEVIN · 2019 to 2023
$2.2M
ENaC-α mediates lung fluid clearance and capillary barrier function in pneumoniaR01HL138410 · NHLBI · AUGUSTA UNIVERSITY · PI LUCAS, RUDOLF · 2018 to 2021
$2.0M
Lipid macropinocytosis: a novel target in atherosclerotic cardiovascular diseaseR01HL139562 · NHLBI · AUGUSTA UNIVERSITY · PI CSANYI, GABOR · 2018 to 2022
$1.9M
A Novel Role of Macrophage TSP1-CD47 Signaling in AtherosclerosisR00HL114648 · NHLBI · AUGUSTA UNIVERSITY · PI CSANYI, GABOR · 2015 to 2017
$747k
Regulation of Lymphangiogenesis by Thrombospondin 1R00HL146954 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SINGLA, BHUPESH · 2022 to 2024
$739k
Regulation of Lymphangiogenesis by Thrombospondin 1K99HL146954 · NHLBI · AUGUSTA UNIVERSITY · PI SINGLA, BHUPESH · 2020 to 2021
$232k
Mechanisms of foamy monocyte formation in atherosclerosisF31HL162498 · NHLBI · AUGUSTA UNIVERSITY · PI AHN, WONMO · 2022 to 2024
$105k
NEI NIH HHS R01 EY029318NHLBI NIH HHS F31 HL162498NHLBI NIH HHS K99 HL146954NHLBI NIH HHS R00 HL114648NHLBI NIH HHS R00 HL146954NHLBI NIH HHS R01 HL138410NHLBI NIH HHS R01 HL139562
6 · The paper itself

Abstract

Accumulation of lipid-laden foam cells in the arterial wall plays a central role in atherosclerotic lesion development, plaque progression, and late-stage complications of atherosclerosis. However, there are still fundamental gaps in our knowledge of the underlying mechanisms leading to foam cell formation in atherosclerotic arteries. Here, we investigated the role of receptor-independent macropinocytosis in arterial lipid accumulation and pathogenesis of atherosclerosis. Genetic inhibition of fluid-phase macropinocytosis in myeloid cells (

Indexed as

AtherosclerosisFoam CellsAnimalsApolipoproteins EArteriesCD36 AntigensHumansLipoproteins, LDLMiceMice, KnockoutApolipoproteins ECD36 AntigensLipoproteins, LDL

Identifiers

PMID36130017
PMCPMC9645012
OpenAlexW4296564605

What OpenQuestion holds

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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.