Evidence map›Paper›PMID 32142630›Full record

ArticleDevelopmental cell2020

Smooth Muscle Differentiation Is Essential for Airway Size, Tracheal Cartilage Segmentation, but Dispensable for Epithelial Branching.

Randee E Young, Mary-Kayt Jones, Elizabeth A Hines, Rongbo Li, Yongfeng Luo, Wei Shi, Jamie M Verheyden, Xin Sun

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
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  12. Review
  13. The lung mesenchyme in development, regeneration, and fibrosis.The Journal of clinical investigation · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Anti-asthmatic miR-224-5p inhibits the FHL1/MAPK pathway to repress airway smooth muscle cell proliferation in a murine model of asthma-like airway inflammation.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2022
    Article
  18. Article
  19. BMP4 and Wnt signaling interact to promote mouse tracheal mesenchyme morphogenesis.American journal of physiology. Lung cellular and molecular physiology · 2022
    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

8 authors at 3 institutions in 1 country.

Randee E YoungDepartment of Pediatrics, University of California-San Diego, La Jolla, CA 92093, USA; Laboratory of Genetics, Department of Medical Genetics, University of Wisconsin-Madison, Madison, WI 53706, USA.
Mary-Kayt JonesLaboratory of Genetics, Department of Medical Genetics, University of Wisconsin-Madison, Madison, WI 53706, USA.
Elizabeth A HinesLaboratory of Genetics, Department of Medical Genetics, University of Wisconsin-Madison, Madison, WI 53706, USA.
Rongbo LiDepartment of Pediatrics, University of California-San Diego, La Jolla, CA 92093, USA.
Yongfeng LuoDevelopmental Biology and Regenerative Medicine Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.
Wei ShiDevelopmental Biology and Regenerative Medicine Program, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.
Jamie M VerheydenDepartment of Pediatrics, University of California-San Diego, La Jolla, CA 92093, USA. Electronic address: jverheyden@ucsd.edu.
Xin SunDepartment of Pediatrics, University of California-San Diego, La Jolla, CA 92093, USA; Department of Biological Sciences, University of California-San Diego, La Jolla, CA 92093, USA. Electronic address: xinsun@ucsd.edu.
University of California, San Diego · USChildren's Hospital of Los Angeles · USUniversity of Wisconsin–Madison · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007133 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PERNA, NICOLE T · 1985 to 2023
$16.5M
U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
Functional Genomics of Stress Defense in YeastR01GM083989 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI GASCH, AUDREY · 2008 to 2016
$3.0M
Impact of Early-in-life Disruption of Lung Development on Adult Lung Progenitor FunctionR01HL143256 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PRINCE, LAWRENCE S, SUN, XIN · 2018 to 2021
$2.1M
Cartilage and Smooth Muscle in Airway Tone and MicroenvironmentR01HL119946 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI SUN, XIN · 2014 to 2017
$2.1M
Genetic Basis of Normal and Pathological Alveologenesis in Lung DevelopmentR01HL142215 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUN, XIN · 2018 to 2021
$2.0M
Respiratory Deficiencies in Congenital Diaphragmatic HerniaR01HL122406 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI SUN, XIN · 2015 to 2018
$1.8M
NHLBI NIH HHS R01 HL119946NHLBI NIH HHS R01 HL122406NHLBI NIH HHS R01 HL142215NHLBI NIH HHS R01 HL143256NIGMS NIH HHS R01 GM083989NIGMS NIH HHS T32 GM007133NINDS NIH HHS P30 NS047101
6 · The paper itself

Abstract

Airway smooth muscle is best known for its role as an airway constrictor in diseases such as asthma. However, its function in lung development is debated. A prevalent model, supported by in vitro data, posits that airway smooth muscle promotes lung branching through peristalsis and pushing intraluminal fluid to branching tips. Here, we test this model in vivo by inactivating Myocardin, which prevented airway smooth muscle differentiation. We found that Myocardin mutants show normal branching, despite the absence of peristalsis. In contrast, tracheal cartilage, vasculature, and neural innervation patterns were all disrupted. Furthermore, airway diameter is reduced in the mutant, counter to the expectation that the absence of smooth muscle constriction would lead to a more relaxed and thereby wider airway. These findings together demonstrate that during development, while airway smooth muscle is dispensable for epithelial branching, it is integral for building the tracheal architecture and promoting airway growth.

Indexed as

AnimalsCartilageCell DifferentiationEpithelial CellsLungMorphogenesisMuscle ContractionMuscle, SmoothMyocardinNuclear ProteinsTrans-ActivatorsMyocardinNuclear ProteinsTrans-Activatorsairway sizebranching morphogenesiscartilage developmentdevelopmentlungmouse geneticsMyocdperistalsissmooth muscle celltrachea

Identifiers

PMID32142630
PMCPMC7540204
OpenAlexW3009052656

What OpenQuestion holds

Textmetadata
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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.