Evidence map›Paper›PMID 21724861›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2011

Lipopolysaccharide-induced injury is more pronounced in fetal transgenic ErbB4-deleted lungs.

Andreas Schmiedl, Jan Behrens, Katja Zscheppang, Erkhembulgan Purevdorj, Dietlinde von Mayersbach, Andrea Liese, Christiane E L Dammann

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  5. Review
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  7. Review
  8. Review
  9. Loss of lung WWOX expression causes neutrophilic inflammation.American journal of physiology. Lung cellular and molecular physiology · 2017
    Article
  10. Article
  11. Intra-amniotic LPS and antenatal betamethasone: inflammation and maturation in preterm lamb lungs.American journal of physiology. Lung cellular and molecular physiology · 2012
    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

7 authors at 1 institution in 2 countries.

Andreas SchmiedlInstitute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
Jan Behrens
Katja Zscheppang
Erkhembulgan Purevdorj
Dietlinde von Mayersbach
Andrea Liese
Christiane E L Dammann
Medizinische Hochschule Hannover · DE

Funding

How Dose Androgen Inhibit Fetal MaturationR01HL037930 · NHLBI · TUFTS MEDICAL CENTER · PI NIELSEN, HEBER C. · 1986 to 2010
$3.0M
NEUREGULINS AND THEIR RECEPTORS IN LUNG DEVELOPMENTK08HL004436 · NHLBI · TUFTS MEDICAL CENTER · PI DAMMANN, CHRISTIANE E · 2001 to 2005
$649k
NHLBI NIH HHS HL-037930NHLBI NIH HHS HL-04436
6 · The paper itself

Abstract

Pulmonary ErbB4 deletion leads to a delay in fetal lung development, alveolar simplification, and lung function disturbances in adult mice. We generated a model of intrauterine infection in ErbB4 transgenic mice to study the additive effects of antenatal LPS administration and ErbB4 deletion during fetal lung development. Pregnant mice were treated intra-amniotically with an LPS dose of 4 μg at E17 of gestation. Lungs were analyzed 24 h later. A significant influx of inflammatory cells was seen in all LPS-treated lungs. In heterozygote control lungs, LPS treatment resulted in a delay of lung morphogenesis characterized by a significant increase in the fraction of mesenchyme, a decrease in gas exchange area, and disorganization of elastic fibers. Surfactant protein (Sftp)b and Sftpc were upregulated, but mRNA of Sftpb and Sftpc was downregulated compared with non-LPS-treated controls. The mRNA of Sftpa1 and Sftpd was upregulated. In ErbB4-deleted lungs, the LPS effects were more pronounced, resulting in a further delay in morphological development, a more pronounced inflammation in the parenchyma, and a significant higher increase in all Sftp. The effect on Sftpb and Sftpc mRNA was somewhat different, resulting in a significant increase. These results imply a major role of ErbB4 in LPS-induced signaling in structural and functional lung development.

Indexed as

Alveolar Epithelial CellsAnimalsCell MovementElastic TissueErbB ReceptorsFemaleFetusGene Expression Regulation, DevelopmentalInflammationIntercellular Signaling Peptides and ProteinsLipopolysaccharidesLungMiceMice, KnockoutPeptidesPregnancyErbb4 protein, mouseErbB ReceptorsIntercellular Signaling Peptides and ProteinsLipopolysaccharidesPeptidesProtein IsoformsPulmonary Surfactant-Associated Protein CReceptor, ErbB-4RNA, MessengerSftpc protein, mouse

Identifiers

PMID21724861
PMCPMC3191748
OpenAlexW2047316934

What OpenQuestion holds

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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.