Evidence map›Paper›PMID 33472399›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2021

Resolvin D1 Enhances Necroptotic Cell Clearance Through Promoting Macrophage Fatty Acid Oxidation and Oxidative Phosphorylation.

Zeinab Hosseini, Michael Marinello, Christa Decker, Brian E Sansbury, Sudeshna Sadhu, Brennan D Gerlach, Ramon Bossardi Ramos, Alejandro P Adam, Matthew Spite, Gabrielle Fredman

Open access · hybridAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

51 citing papers in PubMed, 68 citations in OpenAlex.

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  13. Anti-Atherogenic Mechanisms and Therapies.Current atherosclerosis reports · 2025
    Review
  14. Resolvin D1-mediated cellular crosstalk protects against MASH.JHEP reports : innovation in hepatology · 2025
    Article
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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

10 authors at 5 institutions in 2 countries.

Zeinab Hosseini *The Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Michael Marinello *The Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Christa DeckerThe Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Brian E SansburyCenter for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (B.E.S., M.S.).
Sudeshna SadhuThe Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Brennan D GerlachThe Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Ramon Bossardi RamosThe Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Alejandro P AdamThe Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Matthew SpiteCenter for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (B.E.S., M.S.).
Gabrielle FredmanThe Department of Molecular and Cellular Physiology, Albany Medical College, NY (Z.H., M.M., C.D., S.S., B.D.G., R.B.R., A.P.A., G.F.).
Albany Medical Center Hospital · USBrigham and Women's Hospital · USAlbany Molecular Research (United States) · USInstitut de Biologie Moléculaire et Cellulaire · FRTwitter (United States) · US

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI PETASIS, NICOS A · 2011 to 2020
$14.8M
POSTDOCTORAL TRAINING IN ARTERIOSCLEROSIS RESEARCHT32HL007343 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HENRY N GINSBERG, Muredach P Reilly · 1985 to 2026
$12.7M
NRSA Training CoreTL1TR001875 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SPANN, MARISA N, TAYLOR, JACQUELYN Y · 2016 to 2025
$8.9M
Role of Inflammation-Resolving Lipid Mediators In Ischemic RevascularizationR01HL106173 · NHLBI · UNIVERSITY OF LOUISVILLE · PI SPITE, MATTHEW R · 2011 to 2023
$5.7M
Senescence dysregulates of inflammation-resolution programs in atherosclerosisR01HL153019 · NHLBI · ALBANY MEDICAL COLLEGE · PI FREDMAN, GABRIELLE · 2020 to 2023
$2.6M
Necroptosis Impairs Inflammation-Resolution Programs in AtherosclerosisR01HL141127 · NHLBI · ALBANY MEDICAL COLLEGE · PI FREDMAN, GABRIELLE · 2018 to 2022
$2.2M
Role of endothelial JAK/STAT signaling in the regulation of vascular leakageR01GM124133 · NIGMS · ALBANY MEDICAL COLLEGE · PI ADAM, ALEJANDRO PABLO · 2018 to 2022
$2.2M
NCATS NIH HHS TL1 TR001875NCATS NIH HHS UL1 TR001873NHLBI NIH HHS R01 HL106173NHLBI NIH HHS R01 HL141127NHLBI NIH HHS R01 HL153019NHLBI NIH HHS T32 HL007343NIGMS NIH HHS P01 GM095467NIGMS NIH HHS R01 GM124133
6 · The paper itself

Abstract

objectivePlaque necrosis is a key feature of defective resolution in atherosclerosis. Recent evidence suggests that necroptosis promotes plaque necrosis; therefore, we sought to determine how necroptotic cells (NCs) impact resolution programs in plaques. Approach and Results: To investigate the role(s) of necroptosis in advanced atherosclerosis, we used mice deficient of

conclusionsThese results suggest that NCs derange resolution by limiting key SPMs and impairing the efferocytic repertoire of macrophages. Moreover, these findings provide a molecular mechanism for RvD1 in directing proresolving metabolic programs in macrophages and further suggests RvD1 as a potential therapeutic strategy to limit NCs in tissues. Graphic Abstract: A graphic abstract is available for this article.

Indexed as

15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAMP-Activated Protein KinasesAnimalsApoptosisDocosahexaenoic AcidsFatty AcidsFemaleMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutNecroptosisNecrosisOxidative PhosphorylationPhagocytosis15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAMP-Activated Protein KinasesDocosahexaenoic AcidsFatty AcidsMLKL protein, mouseProstaglandinsProtein Kinasesresolvin D1atherosclerosismacrophagenecroptosisresolvinthromboxane

Identifiers

PMID33472399
PMCPMC8174560
OpenAlexW3125899274

What OpenQuestion holds

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Read underepoch 390

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.