Evidence map›Paper›PMID 20966396›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2011

Toll-like receptor 9 signaling is critical for early experimental deep vein thrombosis resolution.

Peter K Henke, Mayo Mitsuya, Catherine E Luke, Megan A Elfline, Joseph F Baldwin, K Barry Deatrick, Jose A Diaz, Vikram Sood, Gilbert R Upchurch, Thomas W Wakefield and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.7field-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

43 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Immune cell-mediated venous thrombus resolution.Research and practice in thrombosis and haemostasis · 2023
    Review
  5. Review
  6. Article
  7. Inflammation in Cerebral Venous Thrombosis.Frontiers in immunology · 2022
    Review
  8. Review
  9. Insights from experimental post-thrombotic syndrome and potential for novel therapies.Translational research : the journal of laboratory and clinical medicine · 2020
    Review
  10. The effect of anesthetics on toll like receptor 9.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  11. Article
  12. Review
  13. Resolution of Deep Venous Thrombosis: Proposed Immune Paradigms.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Serpins in Venous Thrombosis and Venous Thrombus Resolution.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
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

12 authors at 1 institution in 1 country.

Peter K HenkeCVC-5463, Ann Arbor, MI 48109, USA. henke@umich.edu
Mayo Mitsuya
Catherine E Luke
Megan A Elfline
Joseph F Baldwin
K Barry Deatrick
Jose A Diaz
Vikram Sood
Gilbert R Upchurch
Thomas W Wakefield
Cory Hogaboam
Steven L Kunkel
University of Michigan · US

Funding

Vein Wall Fibrotic Injury After DVT is SLC-CCR7 DependentR01HL092129 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HENKE, PETER K · 2009 to 2012
$1.5M
Vein wall remodeling after DVT is matrix metalloproteinase dependentR01HL083918 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HENKE, PETER K · 2006 to 2009
$1.4M
NHLBI NIH HHS HL083918NHLBI NIH HHS HL092129NHLBI NIH HHS R01 HL083918NHLBI NIH HHS R01 HL092129
6 · The paper itself

Abstract

objectiveToll-like receptors (TLR) bridge innate immunity and host responses, including inflammation. Sterile inflammation such as a venous thrombus (Vt) may involve TLR signaling, including TLR9. METHODS AND

resultsTLR9 signaling on thrombus resolution was investigated using a mouse model of stasis Vt. Vt were significantly larger in TLR9-/- mice compared with wild-type (WT) at 2 and 8 days, despite a 2-fold increase in thrombus polymorphonucleic neutrophils at 2 days and monocytes at 8 days, whereas thrombus collagen and neovascularization was 55% and 37% less, respectively, at 8 days. Coincidently, decreased fibrinogen and increased thrombin-antithrombin complex were observed in TLR9-/- mouse thrombi. Vein wall interferon-α, interleukin-1α, and interleukin-2 were significantly reduced in TLR9-/- mice compared with WT. Thrombus cell death pathway markers were not significantly altered at 2 days, but caspase-1 was reduced in TLR9-/- thrombi at 8 days. MyD88 confers TLR9 intracellular signaling, but MyD88-/- mice had Vt resolution similar to that of WT. However, inhibition of the NOTCH ligand δ-like 4 was associated with larger Vt. Finally, stimulation with a TLR9 agonist was associated with smaller Vt.

conclusionsTLR9 signaling is integral for early and mid-Vt resolution through modulation of sterile inflammation, maintaining a TH1 milieu, and effects on the thrombosis pathway.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAnimalsAntithrombin IIIBlood CoagulationCalcium-Binding ProteinsCollagenCytokinesDisease Models, AnimalFibrinogenInflammationIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsMiceMice, Inbred BALB CAdaptor Proteins, Signal TransducingAntithrombin IIIantithrombin III-protease complexCalcium-Binding ProteinsCollagenCytokinesDLL4 protein, mouseFibrinogenIntracellular Signaling Peptides and ProteinsMembrane ProteinsMyd88 protein, mouseMyeloid Differentiation Factor 88OligodeoxyribonucleotidesPeptide HydrolasesTlr9 protein, mouseToll-Like Receptor 9

Identifiers

PMID20966396
PMCPMC3005132
OpenAlexW2169347963

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.