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Therapeutically inhibiting macrophage necroptosis reduces inflammation‐driven atherosclerosis and promotes plaque stability

2017· article· en· W4389022264 on OpenAlexaff
Denuja Karunakaran, Michèle Geoffrion, Richard Lee, Lihui Wei, Wei Gan, Ljubica Perisic, Lars Mäegdefessel, Ulf Hedin, Subash Sad, Liang Guo, Frank D. Kolodgie, Terrence D. Ruddy, Renu Virmani, Katey J. Rayner

Bibliographic record

VenueThe FASEB Journal · 2017
Typearticle
Languageen
FieldImmunology and Microbiology
TopicPhagocytosis and Immune Regulation
Canadian institutionsUniversity of Ottawa
Fundersnot available
KeywordsNecroptosisInflammationProgrammed cell deathApoptosisMacrophageCancer researchCytokineProinflammatory cytokineTumor necrosis factor alphaFoam cellMacrophage polarizationChemistryImmunologyCell biologyBiologyIn vitroBiochemistry

Abstract

fetched live from OpenAlex

Atherosclerosis is a maladaptive disease driven primarily by macrophages. As the atherosclerotic plaque progresses, inflammatory and macrophage cell death pathways drive the formation of complex, unstable and rupture‐prone lesions with large necrotic core(s). Necroptosis is an emerging cell death pathway involving RIP1, RIP3 and MLKL kinases that, in contrast to apoptosis, induces a pro‐inflammatory state. We hypothesize that inhibiting RIP1 and RIP3 reduces macrophage inflammation and necroptosis to reduce atherosclerosis. Oxidized LDL (oxLDL) induces necroptotic cell death in macrophages, which can be blocked by Nec‐1, a RIP1‐RIP3 inhibitor. Additionally, RIP3 −/− macrophages are more resistant to oxLDL‐induced cell death. Treatment with oxLDL increased macrophage expression of necroptotic genes RIP1 , RIP3 and MLKL through ROS‐dependent activation of the promoter region. ApoE −/− mice fed a western diet (WD) and simultaneously injected with 100mg/kg RIP1 anti‐sense oligonucleotides (ASO) for 8 weeks had a marked reduction in aortic lesion area compared to both control ASO‐ and PBS‐treated controls (58.8% reduction, p<0.001). In addition, serum inflammatory cytokine profiling suggested a marked reduction in circulating inflammatory cytokines (e.g. IL‐1α, IL‐3 and IL‐17A etc) in RIP1 ASO treated mice compared to control ASO. These results are consistent in vitro , where peritoneal macrophages treated with RIP1 ASO had a reduction in the gene expression of inflammatory genes (e.g. IL‐1α, TNFα) relative to control ASO. Next, in the same experimental model of established atherosclerosis (i.e. Apoe −/− mice fed a western diet for 6 weeks), therapeutic intervention with Nec‐1 these mice reduced lesion size (p<0.05) and increased markers of plaque instability, including reduced necrotic core formation (62.6% reduction, p<0.01). In addition, we developed a novel 123 I‐Nec‐1 radiotracer that targets this pathway to specifically localize to and tightly correlate with atherosclerotic lesions. Lastly, in humans with unstable carotid atherosclerosis, expression of the necroptotic genes RIP1 , RIP3 and MLKL is elevated and MLKL phosphorylation is detected in advanced atheromas, indicating that the necroptotic pathway is highly activated in vulnerable plaques. In conclusion, our findings offer molecular insight into the inflammatory and cell death mechanisms by which atherogenic ligands drives the formation of the vulnerable plaque and identify innovative therapeutic tools to treat atherosclerosis.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.034
GPT teacher head0.259
Teacher spread0.225 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2017
Admission routes1
Has abstractyes

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