Evidence map›Paper›PMID 31604030›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2019

Cell-specific regulatory effects of CXCR2 on cholestatic liver injury.

Takanori Konishi, Rebecca M Schuster, Holly S Goetzman, Charles C Caldwell, Alex B Lentsch

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. A Review of CXCL1 in Cardiac Fibrosis.Frontiers in cardiovascular medicine · 2021
    Pooled it
  2. COX2Physiological reports · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  13. The Role of Inflammation in Cholestatic Liver Injury.Journal of inflammation research · 2023
    Review
  14. The immunological function of CXCR2 in the liver during sepsis.Journal of inflammation (London, England) · 2022
    Review
  15. Article
  16. Review
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

5 authors at 1 institution in 1 country.

Takanori KonishiDepartment of Surgery, University of Cincinnati, College of Medicine, Cincinnati, Ohio.ORCID 0000-0002-4403-8313
Rebecca M SchusterDepartment of Surgery, University of Cincinnati, College of Medicine, Cincinnati, Ohio.
Holly S GoetzmanDepartment of Surgery, University of Cincinnati, College of Medicine, Cincinnati, Ohio.
Charles C CaldwellDepartment of Surgery, University of Cincinnati, College of Medicine, Cincinnati, Ohio.
Alex B LentschDepartment of Surgery, University of Cincinnati, College of Medicine, Cincinnati, Ohio.
University of Cincinnati Medical Center · US

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
REGULATION OF HEPATIC ISCHEMIA/REPERFUSION INJURYR01DK056029 · NIDDK · UNIVERSITY OF LOUISVILLE · PI LENTSCH, ALEX B. · 2000 to 2018
$6.0M
NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R01 DK056029
6 · The paper itself

Abstract

The CXC chemokine receptor 2 (CXCR2) is critical for neutrophil recruitment and hepatocellular viability but has not been studied in the context of cholestatic liver injury following bile duct ligation (BDL). The present study sought to elucidate the cell-specific roles of CXCR2 on acute liver injury after BDL. Wild-type and CXCR2-/- mice were subjected BDL. CXCR2 chimeric mice were created to assess the cell-specific role of CXCR2 on liver injury after BDL. SB225002, a selective CXCR2 antagonist, was administrated intraperitoneally after BDL to investigate the potential of pharmacological inhibition. CXCR2-/- mice had significantly less liver injury than wild-type mice at 3 and 14 days after BDL. There was no difference in biliary fibrosis among groups. The chemokines CXCL1 and CXCL2 were induced around areas of necrosis and biliary structures, respectively, both areas where neutrophils accumulated after BDL. CXCR2-/- mice showed significantly less neutrophil accumulation in those injured areas. CXCR2

Indexed as

LiverReceptors, Interleukin-8BAnimalsCell Migration InhibitionCell MovementChemokine CXCL1Chemokine CXCL2CholestasisDisease Models, AnimalHepatic InfarctionMiceNecrosisNeutrophilsPhenylurea CompoundsProtective AgentsChemokine CXCL1Chemokine CXCL2Cxcl1 protein, mouseCxcl2 protein, mousePhenylurea CompoundsProtective AgentsReceptors, Interleukin-8BSB 225002bile duct ligationchemokinescholestasisneutrophils

Identifiers

PMID31604030
PMCPMC6962495
OpenAlexW2980211740

What OpenQuestion holds

Textmetadata
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.