Evidence map›Paper›PMID 30774009›Full record

ArticleInnate immunity2019

The hepatic innate immune response is lobe-specific in a murine model endotoxemia.

Leanna Nguyen, Jeryl Sandoval, Robyn De Dios, Elesa Yihdego, Miguel Zarate, Odalis Castro, Sarah McKenna, Clyde J Wright

Open access · goldAbstract read
In one paragraph

Article in Innate immunity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Harmonizing mouse anatomy terminology: a common language?Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Review
  2. Article
  3. GSK3β/NF-κB -dependent transcriptional regulation of homeostatic hepatocyteAmerican journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  4. Article
  5. Article
  6. 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

8 authors at 1 institution in 1 country.

Leanna NguyenSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.
Jeryl SandovalSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.
Robyn De DiosSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.
Elesa YihdegoSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.
Miguel ZarateSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.
Odalis CastroSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.
Sarah McKennaSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.
Clyde J WrightSection of Neonatology, Department of Pediatrics, University of Colorado School of Medicine, USA.ORCID 0000-0002-8449-5631
University of Colorado Denver · US

Funding

Role of hepatic IkBb-mediated sustained NFkB activation in neonatal lung injury and abnormal developmentR01HL132941 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI WRIGHT, CLYDE JASON · 2017 to 2021
$2.3M
NHLBI NIH HHS R01 HL132941
6 · The paper itself

Abstract

The liver plays a central role in the innate immune response to endotoxemia. While previous studies have demonstrated lobe-specific transcriptional responses to various insults, whether this is true in response to endotoxemia is unknown. We sought to assess whether there were significant intra- and inter-lobe differences in the murine hepatic innate immune transcriptional response to endotoxemia. Adult male ICR mice were exposed to i.p. LPS (5 mg/kg, 30 min, 60 min, 5 h) and primary ( Tnf, Cxcl1, Nfkbia, Tnfiap3) and secondary ( Il6, Nos2) innate immune response gene expression was assessed in the left medial, right medial, left lateral, and right lateral lobes, and the papillary and caudate processes. The expression of all innate immune response genes increased following i.p. LPS challenge. When tested at the early time points (30 and 60 min), the left medial lobe and caudate process consistently demonstrated the highest induction of gene expression. Most inter-lobe differences were attenuated at later time points (5 h). To improve reproducibility of the study of endotoxemia induced by i.p. LPS challenge, inclusion of appropriate methodological details regarding collection of hepatic tissue should be included when reporting scientific results in published manuscripts.

Indexed as

AnimalsChemokine CXCL1Disease Models, AnimalEndotoxemiaHumansImmunity, InnateInterleukin-6LipopolysaccharidesLiverMaleMiceMice, Inbred ICRNF-kappa BNitric Oxide Synthase Type IITranscriptomeTumor Necrosis Factor-alphaChemokine CXCL1Cxcl1 protein, mouseInterleukin-6LipopolysaccharidesNF-kappa BNitric Oxide Synthase Type IINos2 protein, mouseTumor Necrosis Factor-alphaEndotoxemiainnate immune responseliverprimary response genessecondary response genes

Identifiers

PMID30774009
PMCPMC6784545
OpenAlexW2914325542

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.