Evidence map›Paper›PMID 37166104›Full record

ArticleeLife2023

Hippo signaling impairs alveolar epithelial regeneration in pulmonary fibrosis.

Rachel Warren, Handeng Lyu, Kylie Klinkhammer, Stijn P De Langhe

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

44 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Piezo1 mediates electrotaxis of alveolar epithelial cells via calcium-dependent PI3K/Akt signaling.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. IPF AT2 cells are stuck in transition and biophysically dysfunctional.bioRxiv : the preprint server for biology · 2026
    Article
  12. Article
  13. Mechanobiology and Resolution of Lung Fibrosis.Annual review of physiology · 2026
    Review
  14. Review
  15. Review
  16. Targeting the epithelium in pulmonary fibrosis.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  17. Review
  18. Review
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Rachel Warren *Department of Medicine, Division of Pulmonary and Critical Medicine, Mayo Clinic, Rochester, United States.ORCID 0000-0001-9438-2975
Handeng Lyu *Department of Medicine, Division of Pulmonary and Critical Medicine, Mayo Clinic, Rochester, United States.
Kylie KlinkhammerDepartment of Medicine, Division of Pulmonary and Critical Medicine, Mayo Clinic, Rochester, United States.
Stijn P De LangheDepartment of Medicine, Division of Pulmonary and Critical Medicine, Mayo Clinic, Rochester, United States.ORCID 0000-0003-3867-4572
Mayo Clinic in Arizona · US

Funding

Cell competition in pulmonary fibrosis and ARDSR35HL161169 · NHLBI · MAYO CLINIC ROCHESTER · PI Stijn Piet Johan De Langhe · 2022 to 2026
$4.7M
Interdisciplinary Training in Lung Physiology and Biomedical EngineeringT32HL105355 · NHLBI · MAYO CLINIC ROCHESTER · PI PRAKASH, Y. S., SIECK, GARY C. · 2012 to 2021
$3.9M
HL-Lung stem cells and their niches.R01HL132156 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DE LANGHE, STIJN PIET JOHAN · 2016 to 2019
$2.0M
Epithelial stem cell hippo signaling in pulmonary fibrosisR01HL146461 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DE LANGHE, STIJN PIET JOHAN · 2019 to 2021
$1.6M
NHLBI NIH HHS R01 HL132156NHLBI NIH HHS R01 HL146461NHLBI NIH HHS R35 HL161169NHLBI NIH HHS T32 HL105355
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) consists of fibrotic alveolar remodeling and progressive loss of pulmonary function. Genetic and experimental evidence indicates that chronic alveolar injury and failure to properly repair the respiratory epithelium are intrinsic to IPF pathogenesis. Loss of alveolar type 2 (AT2) stem cells or mutations that either impair their self-renewal and/or impair their differentiation into AT1 cells can serve as a trigger of pulmonary fibrosis. Recent reports indicate increased YAP activity in respiratory epithelial cells in IPF lungs. Individual IPF epithelial cells with aberrant YAP activation in bronchiolized regions frequently co-express AT1, AT2, conducting airway selective markers and even mesenchymal or EMT markers, demonstrating 'indeterminate' states of differentiation and suggesting that aberrant YAP signaling might promote pulmonary fibrosis. Yet, Yap and Taz have recently also been shown to be important for AT1 cell maintenance and alveolar epithelial regeneration after

Indexed as

Hippo Signaling PathwayIdiopathic Pulmonary FibrosisAdaptor Proteins, Signal TransducingBleomycinHumansIntracellular Signaling Peptides and ProteinsLungTranscription FactorsAdaptor Proteins, Signal TransducingBleomycinIntracellular Signaling Peptides and ProteinsTranscription Factorsfibrosishippolungmouseregenerative medicinestem cellstem cellsTazYap

Identifiers

PMID37166104
PMCPMC10208641
OpenAlexW4376133418

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.