Evidence map›Paper›PMID 36154712›Full record

ArticleeLife2022

Fibroblast-derived

Elizabeth M Sefton, Mirialys Gallardo, Claire E Tobin, Brittany C Collins, Mary P Colasanto, Allyson J Merrell, Gabrielle Kardon

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Feasibility of invasive neurally-adjusted ventilatory assist in severe congenital diaphragmatic hernia.Journal of perinatology : official journal of the California Perinatal Association · 2026
    Observational
  3. Modeling patient variants ofbioRxiv : the preprint server for biology · 2026
    Article
  4. Mesenchymal retinoic acid signaling is required for normal diaphragm development in mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. 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

7 authors at 1 institution in 1 country.

Elizabeth M SeftonDepartment of Human Genetics, University of Utah, Salt Lake City, United States.ORCID 0000-0001-6481-612X
Mirialys GallardoDepartment of Human Genetics, University of Utah, Salt Lake City, United States.
Claire E TobinDepartment of Human Genetics, University of Utah, Salt Lake City, United States.
Brittany C CollinsDepartment of Human Genetics, University of Utah, Salt Lake City, United States.
Mary P ColasantoDepartment of Human Genetics, University of Utah, Salt Lake City, United States.
Allyson J MerrellAmbys Medicines, South San Francisco, United States.
Gabrielle KardonDepartment of Human Genetics, University of Utah, Salt Lake City, United States.ORCID 0000-0003-2144-4463
University of Utah · US

Funding

Interdisciplinary Training Program in MetabolismT32DK091317 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI SCOTT A SUMMERS · 2011 to 2026
$4.8M
Genetic and Environmental Regulation of Diaphragm Development and Congenital Diaphragmatic HerniasR01HD104317 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI KARDON, GABRIELLE · 2021 to 2025
$2.4M
Development of the Diaphragm and Congenital Diaphragmatic Hernias (CDH)R01HD087360 · NICHD · UNIVERSITY OF UTAH · PI KARDON, GABRIELLE · 2016 to 2020
$1.6M
Biophysical and genetic mechanisms underlying diaphragm morphogenesis and Congenital Diaphragmatic HerniasK99HD101682 · NICHD · UNIVERSITY OF UTAH · PI SEFTON, ELIZABETH MARIE · 2020 to 2022
$323k
The role of connective tissue in regulating muscularization and innervation of the diaphragmF32HD093425 · NICHD · UNIVERSITY OF UTAH · PI SEFTON, ELIZABETH MARIE · 2017 to 2019
$187k
NICHD NIH HHS F32 HD093425NICHD NIH HHS K99 HD101682NICHD NIH HHS R01 HD087360NICHD NIH HHS R01 HD104317NIDDK NIH HHS T32 DK091317
6 · The paper itself

Abstract

The diaphragm is a domed muscle between the thorax and abdomen essential for breathing in mammals. Diaphragm development requires the coordinated development of muscle, connective tissue, and nerve, which are derived from different embryonic sources. Defects in diaphragm development cause the common and often lethal birth defect, congenital diaphragmatic hernias (CDH). HGF/MET signaling is required for diaphragm muscularization, but the source of HGF and the specific functions of this pathway in muscle progenitors and effects on phrenic nerve have not been explicitly tested. Using conditional mutagenesis in mice and pharmacological inhibition of MET, we demonstrate that the pleuroperitoneal folds (PPFs), transient embryonic structures that give rise to the connective tissue in the diaphragm, are the source of HGF critical for diaphragm muscularization. PPF-derived HGF is directly required for recruitment of MET+ muscle progenitors to the diaphragm and indirectly (via its effect on muscle development) required for phrenic nerve primary branching. In addition, HGF is continuously required for maintenance and motility of the pool of progenitors to enable full muscularization. Localization of HGF at the diaphragm's leading edges directs dorsal and ventral expansion of muscle and regulates its overall size and shape. Surprisingly, large muscleless regions in

Indexed as

DiaphragmHernias, Diaphragmatic, CongenitalAnimalsDisease Models, AnimalFibroblastsMammalsMiceMorphogenesisPhenyl EthersThoraxPhenyl EthersCDHcell culturedevelopmental biologydiaphragmfibroblastsgeneticsgenomicsHGFMETmousemuscle

Identifiers

PMID36154712
PMCPMC9514848
OpenAlexW4297256583

What OpenQuestion 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 OpenQuestion graph.