Evidence map›Paper›PMID 30359200›Full record

ArticleCirculation research2018

Transcriptome Analysis Reveals Nonfoamy Rather Than Foamy Plaque Macrophages Are Proinflammatory in Atherosclerotic Murine Models.

Kyeongdae Kim, Dahee Shim, Jun Seong Lee, Konstantin Zaitsev, Jesse W Williams, Ki-Wook Kim, Man-Young Jang, Hyung Seok Jang, Tae Jin Yun, Seung Hyun Lee and 13 more

Open access · greenAbstract read
In one paragraph

Article in Circulation research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 293 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
293citing papers in PubMed, 1 pooled it
13.8field-weighted citation impact, top 1% 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

293 citing papers in PubMed, 1 synthesis or guideline pooled it, 427 citations in OpenAlex.

  1. Pooled it
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  20. Research progress on macrophage regulation of atherosclerosis.Frontiers in cardiovascular medicine · 2026
    Review

233 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 3 countries.

Kyeongdae KimFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Dahee ShimFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Jun Seong LeeLaboratory of Cellular Physiology and Immunology (J.S.L., T.J.Y., C.C.), Institut de Recherches Cliniques de Montréal, Canada.
Konstantin ZaitsevDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO (K.Z., J.W.W., K.-W.K., G.J.R., M.N.A.).
Jesse W WilliamsDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO (K.Z., J.W.W., K.-W.K., G.J.R., M.N.A.).
Ki-Wook KimDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO (K.Z., J.W.W., K.-W.K., G.J.R., M.N.A.).
Man-Young JangFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Hyung Seok JangFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Tae Jin YunLaboratory of Cellular Physiology and Immunology (J.S.L., T.J.Y., C.C.), Institut de Recherches Cliniques de Montréal, Canada.
Seung Hyun LeeFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Won Kee YoonBiomedical Mouse Resource Center, Korean Research Institute of Bioscience and Biotechnology (KRIBB), Chungbuk, Republic of Korea (W.K.Y.).
Annik PratLaboratory of Biochemical Neuroendocrinology (A.P., N.G.S.), Institut de Recherches Cliniques de Montréal, Canada.
Nabil G SeidahLaboratory of Biochemical Neuroendocrinology (A.P., N.G.S.), Institut de Recherches Cliniques de Montréal, Canada.
Jungsoon ChoiDepartment of Mathematics (J.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Seung-Pyo LeeCardiovascular Center and Department of Internal Medicine, Seoul National University Hospital, Republic of Korea (S.-P.L.).
Sang-Ho YoonFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Jin Wu NamFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Je Kyung SeongLaboratory of Developmental Biology and Genomics, Research Institute for Veterinary Science, College of Veterinary Medicine, Korea Mouse Phenotyping Center, Seoul National University, Republic of Korea (J.K.S.).
Goo Taeg OhDepartment of Life Sciences, Immune and Vascular Cell Network Research Center, National Creative Initiatives, Ewha Womans University, Seoul, Republic of Korea (G.T.O.).
Gwendalyn J RandolphDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO (K.Z., J.W.W., K.-W.K., G.J.R., M.N.A.).
Maxim N ArtyomovDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO (K.Z., J.W.W., K.-W.K., G.J.R., M.N.A.).
Cheolho CheongLaboratory of Cellular Physiology and Immunology (J.S.L., T.J.Y., C.C.), Institut de Recherches Cliniques de Montréal, Canada.
Jae-Hoon ChoiFrom the Department of Life Sciences (K.K., D.S., M.-Y.J., H.S.J., S.H.L., S.-H.Y., J.W.N., J.-H.C.), College of Natural Sciences, Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Hanyang University · KRMontreal Clinical Research Institute · CAWashington University in St. Louis · USEwha Womans University · KRKorea Research Institute of Bioscience and Biotechnology · KRSeoul National University · KR

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
WOMEN'S HEALTH AGENDAU01AI025903 · NIAID · WASHINGTON UNIVERSITY · PI CLIFFORD, DAVID B · 1987 to 2006
$12.5M
DIFFERENTIATION AND FUNCTION OF MONOCYTES AND MACROPHAGESR37AI049653 · NIAID · WASHINGTON UNIVERSITY · PI RANDOLPH, GWENDALYN J · 2016 to 2025
$4.3M
INTEGRATING CELL & LIPOPROTEIN TRAFFICKING WITH VASCULAR BIOLOGY IN HUMAN IBDDP1DK109668 · NIDDK · WASHINGTON UNIVERSITY · PI RANDOLPH, GWENDALYN J · 2015 to 2019
$3.8M
ATHEROSCLEROTIC LESION INITIATION BY RESIDENT AORTIC MACROPHAGE PROLIFERATION AND LIPID UPTAKEK99HL138163 · NHLBI · WASHINGTON UNIVERSITY · PI WILLIAMS, JESSE WARREN · 2018 to 2018
$125k
CIHR 148363CIHR FRN 125933NCATS NIH HHS UL1 TR002345NCI NIH HHS P30 CA091842NHLBI NIH HHS K99 HL138163NIAID NIH HHS R37 AI049653NIAID NIH HHS U01 AI025903NIDDK NIH HHS DP1 DK109668
6 · The paper itself

Abstract

rationaleMonocyte infiltration into the subintimal space and its intracellular lipid accumulation are the most prominent features of atherosclerosis. To understand the pathophysiology of atherosclerotic disease, we need to understand the characteristics of lipid-laden foamy macrophages in the subintimal space during atherosclerosis.

objectiveWe sought to examine the transcriptomic profiles of foamy and nonfoamy macrophages isolated from atherosclerotic intima. METHODS AND

resultsSingle-cell RNA sequencing analysis of CD45

conclusionsRNA sequencing analysis of intimal macrophages from atherosclerotic aorta revealed that lipid-loaded plaque macrophages are not likely the plaque macrophages that drive lesional inflammation.

Indexed as

TranscriptomeAnimalsAortaCells, CulturedHumansMacrophagesMaleMiceMice, Inbred C57BLPlaque, Atheroscleroticatherosclerosisflow cytometryfoam cellsmacrophagesmiceRNA-seq

Identifiers

PMID30359200
PMCPMC6945121
OpenAlexW2891644675

What OpenQuestion holds

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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.