Evidence map›Paper›PMID 21460221›Full record

ArticleThe Journal of biological chemistry2011

Pattern recognition scavenger receptor CD204 attenuates Toll-like receptor 4-induced NF-kappaB activation by directly inhibiting ubiquitination of tumor necrosis factor (TNF) receptor-associated factor 6.

Xiaofei Yu, Huanfa Yi, Chunqing Guo, Daming Zuo, Yanping Wang, Hyung L Kim, John R Subjeck, Xiang-Yang Wang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

53 citing papers in PubMed, 86 citations in OpenAlex.

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  10. Scavenger receptor A1 participates in uptake ofEmerging microbes & infections · 2021
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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

8 authors at 5 institutions in 3 countries.

Xiaofei YuDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
Huanfa Yi
Chunqing Guo
Daming Zuo
Yanping Wang
Hyung L Kim
John R Subjeck
Xiang-Yang Wang
Institute of Molecular Medicine · INCedars-Sinai Medical Center · USLaboratory of Molecular Genetics · PLRoswell Park Comprehensive Cancer Center · USVirginia Commonwealth University · US

Funding

Large Stress Proteins in Biology and MedicineR01CA154708 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI WANG, XIANG-YANG SHAWN · 2011 to 2015
$1.5M
Scavenger Receptor-A and Immune RegulationR01CA129111 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI WANG, XIANG-YANG SHAWN · 2007 to 2011
$1.2M
NCI NIH HHS CA099362NCI NIH HHS CA129111NCI NIH HHS CA154708NCI NIH HHS R01 CA129111NCI NIH HHS R01 CA154708
6 · The paper itself

Abstract

The collaboration and cross-talk between different classes of innate pattern recognition receptors are crucial for a well coordinated inflammatory response and host defense. Here we report a previously unrecognized role of scavenger receptor A (SRA; also known as CD204) as a signaling regulator in the context of Toll-like receptor 4 (TLR4) activation. We show that SRA/CD204 deficiency leads to greater sensitivity to LPS-induced endotoxic shock. SRA/CD204 down-regulates inflammatory gene expression in dendritic cells by suppressing TLR4-induced activation of the transcription factor NF-κB. For the first time, we demonstrate that SRA/CD204 executes its regulatory functions by directly interacting with the TRAF-C domain of TNF receptor-associated factor 6 (TRAF6), resulting in inhibition of TRAF6 dimerization and ubiquitination. The attenuation of NF-κB activity by SRA/CD204 is independent of its ligand-binding domain, indicating that the signaling-regulatory feature of SRA/CD204 can be uncoupled from its conventional endocytic functions. Collectively, we have identified the molecular linkage between SRA/CD204 and the TLR4 signaling pathways, and our results reveal a novel mechanism by which a non-TLR pattern recognition receptor restricts TLR4 activation and consequent inflammatory response.

Indexed as

AnimalsHEK293 CellsHumansLipopolysaccharidesMiceMice, KnockoutNF-kappa BProtein MultimerizationScavenger Receptors, Class AShock, SepticSignal TransductionTNF Receptor-Associated Factor 6Toll-Like Receptor 4UbiquitinationLipopolysaccharidesMSR1 protein, humanMsr1 protein, mouseNF-kappa BScavenger Receptors, Class ATLR4 protein, humanTlr4 protein, mouseTNF Receptor-Associated Factor 6Toll-Like Receptor 4

Identifiers

PMID21460221
PMCPMC3099696
OpenAlexW2073666490

What OpenQuestion holds

Textmetadata
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.