Evidence map›Paper›PMID 22870324›Full record

ArticlePloS one2012

A key role for the endothelium in NOD1 mediated vascular inflammation: comparison to TLR4 responses.

Timothy Gatheral, Daniel M Reed, Laura Moreno, Peter J Gough, Bart J Votta, Clark A Sehon, David J Rickard, John Bertin, Eric Lim, Andrew G Nicholson and 1 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Endothelial cell, myeloid, and adaptive immune responses in SARS-CoV-2 infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Therapeutic targeting of NOD1 receptors.British journal of pharmacology · 2013
    Review
  15. 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

11 authors at 3 institutions in 3 countries.

Timothy GatheralCardiothoracic Pharmacology, National Heart and Lung Institute, Imperial College, London, United Kingdom.
Daniel M Reed
Laura Moreno
Peter J Gough
Bart J Votta
Clark A Sehon
David J Rickard
John Bertin
Eric Lim
Andrew G Nicholson
Jane A Mitchell
GlaxoSmithKline (United States) · USImperial College London · GBUniversidad Complutense de Madrid · ES

Funding

British Heart Foundation FS/09/017/26810Wellcome TrustWellcome Trust 0852551Z108/Z
6 · The paper itself

Abstract

Understanding the mechanisms by which pathogens induce vascular inflammation and dysfunction may reveal novel therapeutic targets in sepsis and related conditions. The intracellular receptor NOD1 recognises peptidoglycan which features in the cell wall of gram negative and some gram positive bacteria. NOD1 engagement generates an inflammatory response via activation of NFκB and MAPK pathways. We have previously shown that stimulation of NOD1 directly activates blood vessels and causes experimental shock in vivo. In this study we have used an ex vivo vessel-organ culture model to characterise the relative contribution of the endothelium in the response of blood vessels to NOD1 agonists. In addition we present the novel finding that NOD1 directly activates human blood vessels. Using human cultured cells we confirm that endothelial cells respond more avidly to NOD1 agonists than vascular smooth muscle cells. Accordingly we have sought to pharmacologically differentiate NOD1 and TLR4 mediated signalling pathways in human endothelial cells, focussing on TAK1, NFκB and p38 MAPK. In addition we profile novel inhibitors of RIP2 and NOD1 itself, which specifically inhibit NOD1 ligand induced inflammatory signalling in the vasculature. This paper is the first to demonstrate activation of whole human artery by NOD1 stimulation and the relative importance of the endothelium in the sensing of NOD1 ligands by vessels. This data supports the potential utility of NOD1 and RIP2 as therapeutic targets in human disease where vascular inflammation is a clinical feature, such as in sepsis and septic shock.

Indexed as

AnimalsCells, CulturedEndothelial CellsEndothelium, VascularGram-Negative BacteriaHumansMaleMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMAP Kinase Signaling SystemMuscle, Smooth, VascularNF-kappa BNod1 Signaling Adaptor Proteinp38 Mitogen-Activated Protein KinasesPeptidoglycanRatsMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesNF-kappa BNOD1 protein, humanNod1 Signaling Adaptor Proteinp38 Mitogen-Activated Protein KinasesPeptidoglycanReceptor-Interacting Protein Serine-Threonine Kinase 2RIPK2 protein, humanTLR4 protein, humanTlr4 protein, ratToll-Like Receptor 4

Identifiers

PMID22870324
PMCPMC3411636
OpenAlexW2059850288

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.