Evidence map›Paper›PMID 34685598›Full record

ArticleCells2021

Bile Acids Activate NLRP3 Inflammasome, Promoting Murine Liver Inflammation or Fibrosis in a Cell Type-Specific Manner.

Theresa Maria Holtmann, Maria Eugenia Inzaugarat, Jana Knorr, Lukas Geisler, Marten Schulz, Veerle Bieghs, Mick Frissen, Ariel E Feldstein, Frank Tacke, Christian Trautwein and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Theresa Maria HoltmannDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
Maria Eugenia InzaugaratDepartment of Internal Medicine III, RWTH University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.
Jana KnorrDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
Lukas GeislerDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
Marten SchulzDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.ORCID 0000-0003-0298-0156
Veerle BieghsDepartment of Internal Medicine III, RWTH University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.
Mick FrissenDepartment of Internal Medicine III, RWTH University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.
Ariel E FeldsteinDepartment of Pediatrics, University of California, San Diego, CA 92093, USA.
Frank TackeDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.ORCID 0000-0001-6206-0226
Christian TrautweinDepartment of Internal Medicine III, RWTH University Hospital Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.
Alexander WreeDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.ORCID 0000-0002-2968-1335
Charité - Universitätsmedizin Berlin · DEUniversitätsklinikum Aachen · DEUniversity of California San Diego · US

Funding

Gain of function mutations in inflammasome related genes in human and experimental alcoholic liver diseaseR01AA024206 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FELDSTEIN, ARIEL · 2019 to 2021
$988k
Deutsche Forschungsgemeinschaft WR173/2-1German Research Foundation SFB/TRR 57NIAAA NIH HHS R01 AA024206
6 · The paper itself

Abstract

Bile acids (BA) as important signaling molecules are considered crucial in development of cholestatic liver injury, but there is limited understanding on the involved cell types and signaling pathways. The aim of this study was to evaluate the inflammatory and fibrotic potential of key BA and the role of distinct liver cell subsets focusing on the NLRP3 inflammasome. C57BL/6 wild-type (WT) and

Indexed as

AnimalsBile Acids and SaltsCells, CulturedHepatic Stellate CellsHepatocytesInflammasomesInflammationKupffer CellsLiver DiseasesMiceMice, Inbred C57BLMice, KnockoutNLR Family, Pyrin Domain-Containing 3 ProteinPrimary Cell CultureBile Acids and SaltsInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousecholestasischolic aciddeoxycholic acidhepatic stellate cellsinflammagensKupffer cellslithocholic acidsterile inflammation

Identifiers

PMID34685598
PMCPMC8534222
OpenAlexW3204507277

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.