Evidence map›Paper›PMID 30156429›Full record

ArticleAmerican journal of respiratory cell and molecular biology2019

Endothelial YAP1 in Regenerative Lung Growth through the Angiopoietin-Tie2 Pathway.

Tadanori Mammoto, Megan Muyleart, Akiko Mammoto

Abstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

31 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Angiogenesis in Lung Regeneration and Aging.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  3. Article
  4. Article
  5. Hippo to the rescue? Advancing technologies in ex vivo lung perfusion.American journal of respiratory cell and molecular biology · 2026
    Article
  6. Article
  7. Blood flow-induced angiocrine signals promote organ growth and regeneration.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  8. Article
  9. Endothelial HRedox biology · 2024
    Article
  10. Review
  11. Article
  12. Inhibition of angiogenesis and regenerative lung growth inFrontiers in cardiovascular medicine · 2024
    Article
  13. Article
  14. Review
  15. Vascular Contribution to Lung Repair and Fibrosis.American journal of respiratory cell and molecular biology · 2023
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  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

3 authors at 2 institutions in 1 country.

Tadanori Mammoto1 Department of Radiology and.
Megan Muyleart1 Department of Radiology and.
Akiko Mammoto2 Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.
Medical College of Wisconsin · USPediatrics and Genetics · US

Funding

LRP5 in age-related changes in lung vascular and epithelial morphogenesisR21AG054830 · NIA · MEDICAL COLLEGE OF WISCONSIN · PI MAMMOTO, AKIKO, MAMMOTO, TADANORI · 2017 to 2018
$418k
NIA NIH HHS R21 AG054830
6 · The paper itself

Abstract

Angiogenesis, the formation of new blood capillaries, plays a key role in organ development and regeneration. Inhibition of lung angiogenesis through the blockade of angiogenic signaling pathways impairs compensatory and regenerative lung growth after unilateral pneumonectomy (PNX). The Hippo signaling transducer, Yes-associated protein (YAP) 1 binds to TEA domain transcription factor (TEAD) and controls organ size and regeneration. However, the role of endothelial YAP1 in lung vascular and alveolar morphogenesis remains unclear. In this report, we demonstrate that knockdown of YAP1 in endothelial cells (ECs) decreases angiogenic factor receptor Tie2 expression, and inhibits EC sprouting and epithelial cell budding in vitro and vascular and alveolar morphogenesis in the gel implanted on the mouse lung. The expression levels of YAP1, TEAD1, and Tie2 increase in ECs isolated from the remaining mouse lungs after unilateral PNX and vascular formation is stimulated in the post-PNX mouse lungs. Knockdown of endothelial YAP1 inhibits compensatory lung growth and vascular and alveolar morphogenesis after unilateral PNX. These findings suggest that endothelial YAP1 is required for lung vascular and alveolar regeneration and modulation of YAP1 in ECs may be novel interventions for the improvement of lung regeneration.

Indexed as

OrganogenesisRegenerationAdaptor Proteins, Signal TransducingAngiopoietinsAnimalsCell Cycle ProteinsCell ProliferationHumansLungMiceMice, KnockoutNeovascularization, PhysiologicPhosphoproteinsPneumonectomyReceptor, TIE-2Signal TransductionAdaptor Proteins, Signal TransducingAngiopoietinsCell Cycle ProteinsPhosphoproteinsReceptor, TIE-2Transcription FactorsYAP1 protein, humanYap1 protein, mouseYAP-Signaling Proteinsangiogenesislung regenerationTEAD1Tie2YAP1

Identifiers

PMID30156429
PMCPMC6348720
OpenAlexW2888943055

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.