Evidence map›Paper›PMID 17553674›Full record

ArticleBiochimica et biophysica acta2007

The ErbB4 receptor in fetal rat lung fibroblasts and epithelial type II cells.

Washa Liu, Katja Zscheppang, Sandy Murray, Heber C Nielsen, Christiane E L Dammann

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Neuregulin-ErbB4 signaling in the developing lung alveolus: a brief review.Journal of cell communication and signaling · 2014
    Article
  6. Article
  7. Article
  8. Lipopolysaccharide-induced injury is more pronounced in fetal transgenic ErbB4-deleted lungs.American journal of physiology. Lung cellular and molecular physiology · 2011
    Article
  9. Article
  10. Article
  11. Article
  12. 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 2 countries.

Washa LiuNewborn Medicine, Department of Pediatrics, Floating Hospital for Children, Tufts-New England Medical Center, Boston, MA 02111, USA. wliu2@tufts-nemc.org
Katja Zscheppang
Sandy Murray
Heber C Nielsen
Christiane E L Dammann
Tufts Medical Center · US

Funding

TUSM/T-NEMC CENTER FOR NEUROSCIENCE RESEARCH - Imaging CoreP30NS047243 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2003 to 2017
$10.0M
PILOT AND FEASIBILITY STUDIESP30DK034928 · NIDDK · TUFTS MEDICAL CENTER · PI PLAUT, ANDREW GEORGE · 1986 to 2007
$8.5M
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 HL04436NHLBI NIH HHS HL37930NHLBI NIH HHS K08 HL004436NHLBI NIH HHS R01 HL037930NIDDK NIH HHS P30 DK034928NIDDK NIH HHS P30 DK34928NINDS NIH HHS P30 NS047243
6 · The paper itself

Abstract

ErbB receptors are important regulators of fetal organ development, including the fetal lung. They exhibit diversity in signaling potential, acting through homo- and heterodimers to cause different biological responses. We hypothesized that ErbB receptors show cell-specific and stimuli-specific activation, heterodimerization, and cellular localization patterns in fetal lung. We investigated this using immunoblotting, co-immunoprecipitation, and confocal microscopy in primary isolated E19 fetal rat lung fibroblasts and epithelial type II cells, stimulated with epidermal growth factor, transforming growth factor alpha, neuregulin 1beta, or treated with conditioned medium (CM) from the respective other cell type. Fetal type II cells expressed significantly more ErbB1, ErbB2, and ErbB3 protein than fibroblasts. ErbB4 was consistently identified by co-immunoprecipitation of all other ErbB receptors in both cell types independent of the treatments. Downregulation of ErbB4 in fibroblasts initiated cell-cell communication that stimulated surfactant phospholipid synthesis in type II cells. Confocal microscopy in type II cells revealed nuclear localization of all receptors, most prominently for ErbB4. Neuregulin treatment resulted in relocation to the extra-nuclear cytoplasmic region, which was distinct from fibroblast CM treatment which led to nuclear localization of ErbB4 and ErbB2, inducing co-localization of both receptors. We speculate that ErbB4 plays a prominent role in fetal lung mesenchyme-epithelial communication.

Indexed as

AnimalsCell CommunicationCulture Media, ConditionedDimerizationDown-RegulationEpithelial CellsErbB ReceptorsFemaleFibroblastsLungMicroscopy, ConfocalPregnancyRatsRats, Sprague-DawleyReceptor, ErbB-4Culture Media, ConditionedErbb4 protein, ratErbB ReceptorsReceptor, ErbB-4

Identifiers

PMID17553674
PMCPMC2144912
OpenAlexW2126665801

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.