Evidence map›Paper›PMID 22906770›Full record

ArticleToxicology2012

Lipopolysaccharide potentiates polychlorinated biphenyl-induced disruption of the blood-brain barrier via TLR4/IRF-3 signaling.

Jeong June Choi, Yean Jung Choi, Lei Chen, Bei Zhang, Sung Yong Eum, Maria T Abreu, Michal Toborek

Abstract read
In one paragraph

Article in Toxicology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  16. Contributions of nonhematopoietic cells and mediators to immune responses: implications for immunotoxicology.Toxicological sciences : an official journal of the Society of Toxicology · 2015
    Review
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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

7 authors at 3 institutions in 1 country.

Jeong June ChoiDepartment of Biochemistry and Molecular Biology, University of Miami School of Medicine, Miami, FL 33136, USA.
Yean Jung Choi
Lei Chen
Bei Zhang
Sung Yong Eum
Maria T Abreu
Michal Toborek
University of Miami · USIcahn School of Medicine at Mount Sinai · USUniversity of Kentucky · US

Funding

Vascular Mechanisms of PCB-Induced Brain MetastasesP42ES007380 · NIEHS · UNIVERSITY OF KENTUCKY · PI PEARSON, KEVIN JOSEPH · 1997 to 2024
$47.8M
Tat, amyloid beta and brain endothelial barrier functionR01MH072567 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Michal Toborek · 2005 to 2026
$7.6M
Implications of caveolae in Tat signaling and integrity of brain endotheliumR01MH063022 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PARK, MIN SEON · 2001 to 2012
$3.1M
Interplay between cArt, HIV, and amyloid at the blood-brain barrier.R01MH098891 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TOBOREK, MICHAL · 2012 to 2016
$1.9M
Exercise as a novel strategy to target methamphetamine-induced cerebrovascular toR01DA027569 · NIDA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TOBOREK, MICHAL · 2009 to 2013
$1.8M
Role of TLR4 in colitis-associated neoplasiaR01CA137869 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ABREU, MARIA TERESA · 2009 to 2013
$1.5M
Exercise-mediated protection against brain metastasesR01CA133257 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TOBOREK, MICHAL · 2010 to 2014
$1.2M
NCI NIH HHS CA133257NCI NIH HHS R01 CA133257NCI NIH HHS R01 CA137869NIDA NIH HHS DA027569NIDA NIH HHS R01 DA027569NIEHS NIH HHS P42 ES007380NIEHS NIH HHS P42 ES 07380NIMH NIH HHS MH072567NIMH NIH HHS MH63022NIMH NIH HHS R01 MH063022NIMH NIH HHS R01 MH072567NIMH NIH HHS R01 MH098891
6 · The paper itself

Abstract

Exposure to polychlorinated biphenyls (PCBs) is associated with numerous adverse health effects. Although the main route of exposure to PCBs is through the gastrointestinal tract, little is known about the contribution of the gut to the health effects of PCBs. We hypothesize that PCBs can disrupt intestinal integrity, causing lipopolysaccharide (LPS) translocation into the bloodstream and potentiation of the systemic toxicity of PCBs. C57BL/6 mice were exposed to individual PCB congeners by oral gavage, followed by the assessment of small intestine morphology and plasma levels of proinflammatory mediators. In addition, mice and human brain endothelial cells were exposed to PCB118 in the presence or absence of LPS to evaluate the contribution of LPS to PCB-induced toxicity at the blood-brain barrier (BBB) level. Oral administration of PCB153, PCB118, or PCB126 disrupted intestinal morphology and increased plasma levels of LPS and proinflammatory cytokines. Direct injection of LPS and PCB118 into the cerebral microvasculature resulted in synergistic disruption of BBB integrity and decreased expression of tight junction proteins in brain microvessels. In vitro experiments confirmed these effects and indicated that stimulation of the toll-like receptor 4 (TLR4) pathway can be responsible for these effects via activation of interferon regulatory factor-3 (IRF-3). These results indicate that LPS may be a contributing factor in PCB-induced dysfunction of the brain endothelium via stimulation of the TLR4/IRF-3 pathway.

Indexed as

Signal TransductionAdministration, OralAnimalsBlood-Brain BarrierCell LineCell MovementCytokinesEndothelial CellsGene SilencingHumansInterferon Regulatory Factor-3LipopolysaccharidesMaleMiceMice, Inbred C57BLPolychlorinated BiphenylsCytokinesInterferon Regulatory Factor-3IRF3 protein, humanLipopolysaccharidesPolychlorinated BiphenylsTLR4 protein, humanToll-Like Receptor 4

Identifiers

PMID22906770
PMCPMC3511608
OpenAlexW2019592184

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.