Evidence map›Paper›PMID 32007503›Full record

ArticleOsteoarthritis and cartilage2020

Role of TLR2 and TLR4 in regulation of articular chondrocyte homeostasis.

Y Wang, X Zhao, R Liu-Bryan

Open access · bronzeAbstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-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

26 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Measuring Joint Pain Through Tibiofemoral Flexion: A Novel Approach to Assess Pain Behavior and Analgesic Profiles in Rats.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
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  11. When DNA-damage responses meet innate and adaptive immunity.Cellular and molecular life sciences : CMLS · 2024
    Review
  12. Article
  13. NOS inhibition reverses TLR2-induced chondrocyte dysfunction and attenuates age-related osteoarthritis.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

3 authors at 2 institutions in 1 country.

Y WangVA San Diego Healthcare System, San Diego, CA, United States; Dept. of Medicine, University of California San Diego, La Jolla, CA, United States.
X ZhaoVA San Diego Healthcare System, San Diego, CA, United States.
R Liu-BryanVA San Diego Healthcare System, San Diego, CA, United States; Dept. of Medicine, University of California San Diego, La Jolla, CA, United States. Electronic address: ruliu@ucsd.edu.
University of California San Diego · USVA San Diego Healthcare System · US

Funding

Cartilage Innate Immunity in OsteoarthritisR01AI081881 · NIAID · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI BRYAN, RU · 2009 to 2013
$1.7M
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 BX002234NIAID NIH HHS R01 AI081881
6 · The paper itself

Abstract

objectiveToll-like receptor (TLR)-mediated catabolic responses are implicated to contribute to osteoarthritis (OA). However, deficiency of TLRs has little chondroprotection in mice in vivo. Here, we studied the effect of deficiency of TLR2 and TLR4 in articular chondrocytes on cellular stress responses in vitro.

designChondrocytes isolated from TLR2 and TLR4 double knockout (TLR2/4dKO) and wild type (WT) mice and recombinant HMGB1 (rHMGB1) and LPS were used. Expression of anti-oxidant and DNA repair enzymes including SOD1, SOD2 and OGG1, and phosphorylation of H2AX (a marker for DNA damage) were examined by Western blotting. MitoSOX Red staining was used for assessing mitochondrial superoxide generation. Autophagic activity was monitored by flow cytometry analysis of mean fluorescence intensity (MFI) of GFP and RFP in chondrocytes transfected with a tandem GFP-mRFP-LC3 plasmid, and by Western blot analysis of expression of LC3 and p62, a selective autophagy adaptor.

resultsBasal expression of SOD2 but not SOD1 was largely reduced in TLR2/4dKO compared to WT chondrocytes, correlated with significantly enhanced menadione-induced mitochondrial superoxide generation (2.85-3.92 and 3.39 to 8.97 with mean difference 3.39 and 6.18 for 25 and 50μM menadione, respectively) and phosphorylation of H2AX. LPS and rHMGB1 induced expression of SOD2, OGG1 and p62 in WT but not TLR2/4dKO chondrocytes. Autophagy flux was impaired in TLR2/4dKO chondrocytes after acute nutrient stress and by LPS and rHMGB1.

conclusionsTLR2 and TLR4 deficiency appears to reduce chondrocyte anti-oxidative stress and autophagy flux capacity, which may compromise cartilage homeostasis as a result of chondrocyte dysfunction.

Indexed as

AnimalsAntioxidantsAutophagyBlotting, WesternCartilage, ArticularChondrocytesDNA DamageDNA GlycosylasesHistonesHMGB1 ProteinHomeostasisLipopolysaccharidesMiceMice, KnockoutMicrotubule-Associated ProteinsMitochondriaAntioxidantsDNA Glycosylasesgamma-H2AX protein, mouseHistonesHMGB1 ProteinLipopolysaccharidesMap1lc3b protein, mouseMicrotubule-Associated ProteinsOgg1 protein, mouseSequestosome-1 ProteinSod1 protein, mouseSqstm1 protein, mouseSuperoxide DismutaseSuperoxide Dismutase-1Superoxide Dismutase 2SuperoxidesTlr2 protein, mouseTlr4 protein, mouseToll-Like Receptor 2Toll-Like Receptor 4Autophagy fluxChondrocytesOxidative stressToll-like receptors

Identifiers

PMID32007503
PMCPMC7214200
OpenAlexW3004156101

What OpenQuestion holds

Textmetadata
LicenceTDM
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.