Evidence map›Paper›PMID 30778349›Full record

ReviewFrontiers in immunology2019

Cell Type-Specific Roles of NF-κB Linking Inflammation and Thrombosis.

Marion Mussbacher, Manuel Salzmann, Christine Brostjan, Bastian Hoesel, Christian Schoergenhofer, Hannes Datler, Philipp Hohensinner, José Basílio, Peter Petzelbauer, Alice Assinger and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 377 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
377citing papers in PubMed, 2 pooled it
23.1field-weighted citation impact, top 1% 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

377 citing papers in PubMed, 2 syntheses or guidelines pooled it, 576 citations in OpenAlex.

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317 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Marion MussbacherInstitute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Vienna, Austria.
Manuel SalzmannInstitute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Vienna, Austria.
Christine BrostjanDepartment of Surgery, General Hospital, Medical University of Vienna, Vienna, Austria.
Bastian HoeselInstitute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Vienna, Austria.
Christian SchoergenhoferDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Hannes DatlerInstitute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Vienna, Austria.
Philipp HohensinnerDivision of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
José BasílioInstitute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Vienna, Austria.
Peter PetzelbauerSkin and Endothelial Research Division, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Alice AssingerInstitute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Vienna, Austria.
Johannes A SchmidInstitute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATVienna General Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor NF-κB is a central mediator of inflammation with multiple links to thrombotic processes. In this review, we focus on the role of NF-κB signaling in cell types within the vasculature and the circulation that are involved in thrombo-inflammatory processes. All these cells express NF-κB, which mediates important functions in cellular interactions, cell survival and differentiation, as well as expression of cytokines, chemokines, and coagulation factors. Even platelets, as anucleated cells, contain NF-κB family members and their corresponding signaling molecules, which are involved in platelet activation, as well as secondary feedback circuits. The response of endothelial cells to inflammation and NF-κB activation is characterized by the induction of adhesion molecules promoting binding and transmigration of leukocytes, while simultaneously increasing their thrombogenic potential. Paracrine signaling from endothelial cells activates NF-κB in vascular smooth muscle cells and causes a phenotypic switch to a "synthetic" state associated with a decrease in contractile proteins. Monocytes react to inflammatory situations with enforced expression of tissue factor and after differentiation to macrophages with altered polarization. Neutrophils respond with an extension of their life span-and upon full activation they can expel their DNA thereby forming so-called neutrophil extracellular traps (NETs), which exert antibacterial functions, but also induce a strong coagulatory response. This may cause formation of microthrombi that are important for the immobilization of pathogens, a process designated as immunothrombosis. However, deregulation of the complex cellular links between inflammation and thrombosis by unrestrained NET formation or the loss of the endothelial layer due to mechanical rupture or erosion can result in rapid activation and aggregation of platelets and the manifestation of thrombo-inflammatory diseases. Sepsis is an important example of such a disorder caused by a dysregulated host response to infection finally leading to severe coagulopathies. NF-κB is critically involved in these pathophysiological processes as it induces both inflammatory and thrombotic responses.

Indexed as

Blood PlateletsCytokinesEndothelial CellsHumansI-kappa B ProteinsInflammationMegakaryocytesMonocytesMuscle, Smooth, VascularNeutrophilsNF-kappa BParacrine CommunicationPlatelet ActivationSepsisSignal TransductionThrombosisCytokinesI-kappa B ProteinsNF-kappa BRELA protein, humanTranscription Factor RelAblood cellscoagulationinflammationNF-kappa B signalingsepsisthrombosisvasculature

Identifiers

PMID30778349
PMCPMC6369217
OpenAlexW2912663500

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.