Evidence map›Paper›PMID 35263587›Full record

ArticleCell reports2022

Monosodium urate crystals regulate a unique JNK-dependent macrophage metabolic and inflammatory response.

Isidoro Cobo, Anyan Cheng, Jessica Murillo-Saich, Roxana Coras, Alyssa Torres, Yohei Abe, Addison J Lana, Johannes Schlachetzki, Ru Liu-Bryan, Robert Terkeltaub and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

41 citing papers in PubMed, 64 citations in OpenAlex.

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  3. Lactate acts as a metabolic brake on inflammation by repressing NLRP3 transcription via NF-κB inhibition.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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

13 authors at 2 institutions in 2 countries.

Isidoro CoboDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, San Diego, CA 92093, USA.
Anyan ChengDivision of Rheumatology, Allergy and Immunology. UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Jessica Murillo-SaichDivision of Rheumatology, Allergy and Immunology. UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Roxana CorasDivision of Rheumatology, Allergy and Immunology. UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA; Department of Medicine, Autonomous University of Barcelona, Plaça Cívica, 08193 Bellaterra, Barcelona, Spain.
Alyssa TorresDivision of Rheumatology, Allergy and Immunology. UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Yohei AbeDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, San Diego, CA 92093, USA.
Addison J LanaDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, San Diego, CA 92093, USA.
Johannes SchlachetzkiDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, San Diego, CA 92093, USA.
Ru Liu-BryanDivision of Rheumatology, Allergy and Immunology. UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA; VA San Diego Healthcare System, 3350 La Jolla Village Drive, San Diego, CA 92161, USA.
Robert TerkeltaubDivision of Rheumatology, Allergy and Immunology. UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA; VA San Diego Healthcare System, 3350 La Jolla Village Drive, San Diego, CA 92161, USA.
Elsa Sanchez-LopezDepartment of Orthopedic Surgery, University of California San Diego, La Jolla, San Diego, CA 92093, USA.
Christopher K GlassDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, San Diego, CA 92093, USA. Electronic address: cglass@heatlh.ucsd.edu.
Monica GumaDivision of Rheumatology, Allergy and Immunology. UCSD School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA; Department of Medicine, Autonomous University of Barcelona, Plaça Cívica, 08193 Bellaterra, Barcelona, Spain; VA San Diego Healthcare System, 3350 La Jolla Village Drive, San Diego, CA 92161, USA. Electronic address: mguma@health.ucsd.edu.
University of California San Diego · USUniversitat Autònoma de Barcelona · ES

Funding

Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrea L Hevener · 2003 to 2026
$40.4M
The Effects of Urate Lowering Therapy on Inflammation, Endothelial function, andP50AR060772 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SINGH, JASVINDER A · 2012 to 2021
$12.8M
Tissue-specific roles of FXR in CVD and NASHP01HL147835 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LOOMBA, ROHIT · 2020 to 2024
$12.2M
Transcriptional co-regulators and macrophage gene expressionR01DK091183 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLASS, CHRISTOPHER K · 2011 to 2025
$9.9M
Rheumatic Diseases Research Training GrantT32AR064194 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GARY S FIRESTEIN, Monica Guma · 2013 to 2026
$3.8M
Targeting hexokinase-2 in rheumatoid arthritisR01AR073324 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUMA, MONICA · 2018 to 2022
$2.4M
Novel Synovial Role in Pathogenesis of GoutR21AR075990 · NIAMS · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI TERKELTAUB, ROBERT A. · 2019 to 2020
$333k
ATP-Citrate Lyase As A Novel Metabolic Target for OsteoarthritisI01BX002234 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI BRYAN, RU · 2015 to 2022
–
BLRD VA I01 BX002234NHLBI NIH HHS P01 HL147835NIAMS NIH HHS P50 AR060772NIAMS NIH HHS R01 AR073324NIAMS NIH HHS R21 AR075990NIAMS NIH HHS T32 AR064194NIDDK NIH HHS P30 DK063491NIDDK NIH HHS R01 DK091183
6 · The paper itself

Abstract

Monosodium urate crystals (MSUc) induce inflammation in vivo without prior priming, raising the possibility of an initial cell-autonomous phase. Here, using genome-wide transcriptomic analysis and biochemical assays, we demonstrate that MSUc alone induce a metabolic-inflammatory transcriptional program in non-primed human and murine macrophages that is markedly distinct to that induced by LPS. Genes uniquely upregulated in response to MSUc belong to lipid and amino acid metabolism, glycolysis, and SLC transporters. This upregulation leads to a metabolic rewiring in sera from individuals and mice with acute gouty arthritis. Mechanistically, the initiating inflammatory-metabolic changes in acute gout flares are regulated through a persistent expression and increased binding of JUN to the promoter of target genes through JNK signaling-but not P38-in a process that is different than after LPS stimulation and independent of inflammasome activation. Finally, pharmacological JNK inhibition limits MSUc-induced inflammation in animal models of acute gouty inflammation.

Indexed as

Arthritis, GoutyUric AcidAnimalsInflammationLipopolysaccharidesMacrophagesMiceLipopolysaccharidesUric AcidAP-1 activationglycolysisgoutJNKmacrophageMSU crystalsSLC2A1transcriptional regulation

Identifiers

PMID35263587
PMCPMC8989403
OpenAlexW4220792903

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.