Evidence map›Paper›PMID 35438721›Full record

ReviewThe Journal of experimental medicine2022

CD36, a signaling receptor and fatty acid transporter that regulates immune cell metabolism and fate.

Yiliang Chen, Jue Zhang, Weiguo Cui, Roy L Silverstein

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 281 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
281citing papers in PubMed, 2 pooled it
33.5field-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

281 citing papers in PubMed, 2 syntheses or guidelines pooled it, 402 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. NADPharmaceutical science advances · 2026
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  17. Macrophage PIM1 Drives Atherosclerosis by Enhancing Foam Cell Formation Via CD36.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Article
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221 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Yiliang ChenDepartment of Medicine, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0001-9786-8305
Jue ZhangVersiti, Blood Research Institute, Milwaukee, WI.ORCID 0000-0001-8331-2496
Weiguo CuiVersiti, Blood Research Institute, Milwaukee, WI.ORCID 0000-0003-1562-9218
Roy L SilversteinDepartment of Medicine, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0001-7859-9154
Medical College of Wisconsin · USVersiti Blood Center of Wisconsin · US

Funding

ERK5 and CD36 link oxidative stress to platelet dysfunction and ischemic injuryR01HL142152 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI MORRELL, CRAIG N, SILVERSTEIN, ROY L · 2019 to 2022
$2.5M
NKA/CD36 signaling in adipocytes promotes oxidative stress and drives chronic inflammation in atherosclerosisR01HL164460 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Yiliang Chen, Roy L Silverstein · 2023 to 2026
$2.1M
Pim1 kinase coordinates PPAR gamma pathway and mitochondrial function to mediate pro-atherogenic responses in macrophagesR01HL153397 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI CUI, WEIGUO, SILVERSTEIN, ROY L · 2021 to 2024
$1.7M
American Heart Association 17SDG33661117American Heart Association-American Stroke Association 17SDG33661117NHLBI NIH HHS R01 HL142152NHLBI NIH HHS R01 HL153397NHLBI NIH HHS R01 HL164460
6 · The paper itself

Abstract

CD36 is a type 2 cell surface scavenger receptor widely expressed in many immune and non-immune cells. It functions as both a signaling receptor responding to DAMPs and PAMPs, as well as a long chain free fatty acid transporter. Recent studies have indicated that CD36 can integrate cell signaling and metabolic pathways through its dual functions and thereby influence immune cell differentiation and activation, and ultimately help determine cell fate. Its expression along with its dual functions in both innate and adaptive immune cells contribute to pathogenesis of common diseases, including atherosclerosis and tumor progression, which makes CD36 and its downstream effectors potential therapeutic targets. This review comprehensively examines the dual functions of CD36 in a variety of immune cells, especially macrophages and T cells. We also briefly discuss CD36 function in non-immune cells, such as adipocytes and platelets, which impact the immune system via intercellular communication. Finally, outstanding questions in this field are provided for potential directions of future studies.

Indexed as

AtherosclerosisFatty AcidsCD36 AntigensHumansMacrophagesMembrane Transport ProteinsSignal TransductionCD36 AntigensCD36 protein, humanFatty AcidsMembrane Transport Proteins

Identifiers

PMID35438721
PMCPMC9022290
OpenAlexW4224226256

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.