Evidence map›Paper›PMID 22227204›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2012

Direct and indirect roles for β-catenin in facultative basal progenitor cell differentiation.

Mary Kathryn Smith, Peter J Koch, Susan D Reynolds

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.9field-weighted citation impact, top 9% 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, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. The role and importance of club cells (Clara cells) in the pathogenesis of some respiratory diseases.Kardiochirurgia i torakochirurgia polska = Polish journal of cardio-thoracic surgery · 2016
    Article
  8. Review
  9. Abnormal epithelial structure and chronic lung inflammation after repair of chlorine-induced airway injury.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  10. Epidermal growth factor receptor activity is necessary for mouse basal cell proliferation.American journal of physiology. Lung cellular and molecular physiology · 2014
    Article
  11. Article
  12. Review
  13. Chemosensory brush cells of the trachea. A stable population in a dynamic epithelium.American journal of respiratory cell and molecular biology · 2013
    Article
  14. Article
  15. β-Catenin and CCNs in lung epithelial repair.American journal of physiology. Lung cellular and molecular physiology · 2013
    Article
  16. Short histological kaleidoscope - recent findings in histology. Part IV.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

3 authors at 2 institutions in 1 country.

Mary Kathryn SmithDepartment of Pediatrics, National Jewish Health, Denver, CO 80206, USA.
Peter J Koch
Susan D Reynolds
University of Colorado Denver · USNational Jewish Health · US

Funding

Wnt Regulation of Tracheobronchial RegenerationR01HL075585 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REYNOLDS, SUSAN D · 2006 to 2010
$1.9M
NHLBI NIH HHS HL075585-S1NHLBI NIH HHS R01 HL075585
6 · The paper itself

Abstract

The conducting airway epithelium is maintained and repaired by endogenous progenitor cells. Dysregulated progenitor cell proliferation and differentiation is thought to contribute to epithelial dysplasia in chronic lung disease. Thus modification of progenitor cell function is an attractive therapeutic goal and one that would be facilitated by knowledge of the molecular pathways that regulate their behavior. We modeled the human tracheobronchial epithelium using primary mouse tracheal epithelial cell cultures that were differentiated by exposure to the air-liquid-interface (ALI). A basal cell subset, termed facultative basal cell progenitors (FBP), initiate these cultures and are the progenitor for tracheal-specific secretory cells, the Clara-like cell, and ciliated cells. To test the hypothesis that β-catenin is necessary for FBP function, ALI cultures were generated from mice homozygous for the Ctnb(flox(E2-6)) allele. In this model, exons 2-6 of the β-catenin gene are flanked by LoxP sites, allowing conditional knockout of β-catenin. The β-catenin locus was modified through transduction with Adenovirus-5-encoding Cre recombinase. This approach generated a mosaic epithelium, comprised of β-catenin wild-type and β-catenin knockout cells. Dual immunostaining and quantitative histomorphometric analyses demonstrated that β-catenin played a direct role in FBP-to-ciliated cell differentiation and that it regulated cell-cell interactions that were necessary for FBP-to-Clara-like cell differentiation. β-catenin was also necessary for FBP proliferation and long-term FBP viability. We conclude that β-catenin is a critical determinant of FBP function and suggest that dysregulation of the β-catenin signaling pathway may contribute to disease pathology.

Indexed as

AllelesAnimalsbeta CateninCell CommunicationCell DifferentiationCell Growth ProcessesCells, CulturedCell SurvivalEpithelial CellsEpitheliumExonsGene ExpressionGene Knockout TechniquesGenetic LociHumansIntegrasesbeta CateninCre recombinaseIntegrases

Identifiers

PMID22227204
PMCPMC3311526
OpenAlexW2082666846

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.