Evidence map›Paper›PMID 22331706›Full record

ArticleStem cells (Dayton, Ohio)2012

NOTCH1 is required for regeneration of Clara cells during repair of airway injury.

Yiming Xing, Aimin Li, Zea Borok, Changgong Li, Parviz Minoo

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

48 citing papers in PubMed, 81 citations in OpenAlex.

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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Yiming XingDepartment of Pediatrics, Division of Neonatology, Will Rogers Institute Pulmonary Research Center, University of Southern California, Keck School of Medicine, Los Angeles, California, USA.
Aimin Li
Zea Borok
Changgong Li
Parviz Minoo
University of Southern California · USRogers (United States) · US

Funding

Molecular programming of AEC differentiation: role of forkhead factorsR37HL062569 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BOROK, ZEA · 2010 to 2014
$2.2M
MECHANISMS OF BPD PATHOGENESISR01HL107307 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MINOO, PARVIZ MINOO · 2012 to 2015
$1.6M
NHLBI NIH HHS R01 HL107307NHLBI NIH HHS R37 HL062569
6 · The paper itself

Abstract

The airways of the mammalian lung are lined with highly specialized epithelial cell types that are the targets of airborne toxicants and injury. Notch signaling plays an important role in the ontogeny of airway epithelial cells, but its contributions to recruitment, expansion or differentiation of resident progenitor/stem cells, and repair and re-establishment of the normal composition of airway epithelium following injury have not been addressed. In this study, the role of a specific Notch receptor, Notch1, was investigated by targeted inactivation in the embryonic lung epithelium using the epithelial-specific Gata5-Cre driver line. Notch1-deficient mice are viable without discernible defects in pulmonary epithelial cell-fate determination and differentiation. However, in an experimental model of airway injury, activity of Notch1 is found to be required for normal repair of the airway epithelium. Absence of Notch1 reduced the ability of a population of cells distinguished by expression of PGP9.5, otherwise a marker of pulmonary neuroendocrine cells, which appears to serve as a reservoir for regeneration of Clara cells. Hairy/enhancer of split-5 (Hes5) and paired-box-containing gene 6 (Pax6) were found to be downstream targets of Notch1. Both Hes5 and Pax6 expressions were significantly increased in association with Clara cell regeneration in wild-type lungs. Ablation of Notch1 reduced Hes5 and Pax6 and inhibited airway epithelial repair. Thus, although dispensable in developmental ontogeny of airway epithelial cells, normal activity of Notch1 is required for repair of the airway epithelium. The signaling pathway by which Notch1 regulates the repair process includes stimulation of Hes5 and Pax6 gene expression.

Indexed as

RegenerationSignal TransductionAnimalsBasic Helix-Loop-Helix ProteinsEye ProteinsGene Expression RegulationHomeodomain ProteinsLung InjuryMiceMice, KnockoutPaired Box Transcription FactorsPAX6 Transcription FactorReceptor, Notch1Repressor ProteinsRespiratory MucosaUbiquitin ThiolesteraseBasic Helix-Loop-Helix ProteinsEye ProteinsHes5 protein, mouseHomeodomain ProteinsNotch1 protein, mousePaired Box Transcription FactorsPax6 protein, mousePAX6 Transcription FactorReceptor, Notch1Repressor ProteinsUbiquitin ThiolesteraseUchl1 protein, mouse

Identifiers

PMID22331706
PMCPMC4005608
OpenAlexW2093119648

What OpenQuestion holds

Textmetadata
LicenceTDM
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.