Evidence map›Paper›PMID 7753811›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

Bombesin and [Leu8]phyllolitorin promote fetal mouse lung branching morphogenesis via a receptor-mediated mechanism.

K A King, J S Torday, M E Sunday

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

15 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
  2. Review
  3. Observational
  4. [Clinical features of neuroendocrine cell hyperplasia of infancy].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2020
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Defective pulmonary innervation and autonomic imbalance in congenital diaphragmatic hernia.American journal of physiology. Lung cellular and molecular physiology · 2012
    Article
  10. Gastrin-releasing peptide blockade as a broad-spectrum anti-inflammatory therapy for asthma.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  11. Bombesin-like peptides modulate alveolarization and angiogenesis in bronchopulmonary dysplasia.American journal of respiratory and critical care medicine · 2007
    Article
  12. Bombesin inhibits alveolarization and promotes pulmonary fibrosis in newborn mice.American journal of respiratory and critical care medicine · 2006
    Article
  13. Review
  14. Article
  15. 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

3 authors at 1 institution in 1 country.

K A KingDepartment of Pediatrics, Children's Hospital, Boston, MA, USA.
J S Torday
M E Sunday
Boston Children's Hospital · US

Funding

Molecular Mechanisms of Lung EmbryogenesisR01HL044984 · NHLBI · DUKE UNIVERSITY · PI SUNDAY, MARY ELIZABETH · 1990 to 2005
$2.7M
NHLBI NIH HHS R01-HL44984
6 · The paper itself

Abstract

Pulmonary neuroendocrine cells are localized predominantly at airway branchpoints. Previous work showed that gastrin-releasing peptide (GRP), a major pulmonary bombesin-like peptide, occurred in neuroendocrine cells exclusively in branching human fetal airways. We now demonstrate that GRP and GRP receptor genes are expressed in fetal mouse lung as early as embryonic day 12 (E12), when lung buds are beginning to branch. By in situ hybridization, GRP receptor transcripts were at highest levels in mesenchymal cells at cleft regions of branching airways and blood vessels. To explore the possibility that bombesin-like peptides might play a role in branching morphogenesis, E12 lung buds were cultured for 48 hr in serum-free medium. In the presence of 0.10-10 microM bombesin, branching was significantly augmented as compared with control cultures, with a peak of 94% above control values at 1 microM (P < 0.005). The bombesin receptor antagonist [Leu13- psi(CH2NH)Leu14]bombesin alone (100 nM) had no effect on baseline branching but completely abolished bombesin-induced branching. A bombesin-related peptide, [Leu8]phyllolitorin also increased branching (65% above control values at 10 nM, P < 0.005). [Leu8]Phyllolitorin also significantly augmented thymidine incorporation in cultured lung buds. Fibronectin, which is abundant at branchpoints, induces GRP gene expression in undifferentiated cell lines. These observations suggest that BLPs secreted by pulmonary neuroendocrine cells may contribute to lung branching morphogenesis. Furthermore, components of branchpoints may induce pulmonary neuroendocrine cell differentiation as part of a positive feedback loop, which could account in part for the high prevalence of these cells at branchpoints.

Indexed as

AnimalsBase SequenceBombesinDNA PrimersFemaleGene ExpressionGestational AgeIn Situ HybridizationLungMiceMice, Inbred StrainsMolecular Sequence DataMorphogenesisOligopeptidesPolymerase Chain ReactionPregnancyBombesinDNA PrimersOligopeptidesphyllolitorinphyllolitorin, Leu-8-Pyrrolidonecarboxylic AcidReceptors, Bombesin

Identifiers

PMID7753811
PMCPMC41943
OpenAlexW2013363497

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.