Evidence map›Paper›PMID 29679560›Full record

ArticleDevelopmental biology2018

Developmental origin and morphogenesis of the diaphragm, an essential mammalian muscle.

Elizabeth M Sefton, Mirialys Gallardo, Gabrielle Kardon

Abstract read
In one paragraph

Article in Developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Modeling patient variants ofbioRxiv : the preprint server for biology · 2026
    Article
  4. Tissue-engineered neuromuscular organoids.Communications biology · 2025
    Article
  5. Review
  6. 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
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Mechanics of Lung Development.Advances in anatomy, embryology, and cell biology · 2023
    Article
  16. Article
  17. Fibroblast-derivedeLife · 2022
    Article
  18. Cellular taxonomy of Hic1Nature communications · 2022
    Article
  19. Review
  20. Congenital diaphragmatic hernia.Nature reviews. Disease primers · 2022
    Review
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 1 institution in 1 country.

Elizabeth M SeftonDepartment of Human Genetics University of Utah, Salt Lake City, UT 84112, USA.
Mirialys GallardoDepartment of Human Genetics University of Utah, Salt Lake City, UT 84112, USA.
Gabrielle KardonDepartment of Human Genetics University of Utah, Salt Lake City, UT 84112, USA.
University of Utah · US

Funding

TRD - VisualizationP41GM103545 · NIGMS · UNIVERSITY OF UTAH · PI JOHNSON, CHRISTOPHER R. · 2012 to 2019
$9.7M
Development of the Diaphragm and Congenital Diaphragmatic Hernias (CDH)R01HD087360 · NICHD · UNIVERSITY OF UTAH · PI KARDON, GABRIELLE · 2016 to 2020
$1.6M
FluoRender: Visualization-Based and Interactive Analysis for Multichannel Microscopy DataR01EB023947 · NIBIB · UNIVERSITY OF UTAH · PI HANSEN, CHARLES · 2017 to 2020
$1.4M
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
NIBIB NIH HHS R01 EB023947NICHD NIH HHS F32 HD093425NICHD NIH HHS R01 HD087360NIGMS NIH HHS P41 GM103545
6 · The paper itself

Abstract

The diaphragm is a mammalian skeletal muscle essential for respiration and for separating the thoracic and abdominal cavities. Development of the diaphragm requires the coordinated development of muscle, muscle connective tissue, tendon, nerves, and vasculature that derive from different embryonic sources. However, defects in diaphragm development are common and the cause of an often deadly birth defect, Congenital Diaphragmatic Hernia (CDH). Here we comprehensively describe the normal developmental origin and complex spatial-temporal relationship between the different developing tissues to form a functional diaphragm using a developmental series of mouse embryos genetically and immunofluorescently labeled and analyzed in whole mount. We find that the earliest developmental events are the emigration of muscle progenitors from cervical somites followed by the projection of phrenic nerve axons from the cervical neural tube. Muscle progenitors and phrenic nerve target the pleuroperitoneal folds (PPFs), transient pyramidal-shaped structures that form between the thoracic and abdominal cavities. Subsequently, the PPFs expand across the surface of the liver to give rise to the muscle connective tissue and central tendon, and the leading edge of their expansion precedes muscle morphogenesis, formation of the vascular network, and outgrowth and branching of the phrenic nerve. Thus development and morphogenesis of the PPFs is critical for diaphragm formation. In addition, our data indicate that the earliest events in diaphragm development are critical for the etiology of CDH and instrumental to the evolution of the diaphragm. CDH initiates prior to E12.5 in mouse and suggests that defects in the early PPF formation or their ability to recruit muscle are an important source of CDH. Also, the recruitment of muscle progenitors from cervical somites to the nascent PPFs is uniquely mammalian and a key developmental innovation essential for the evolution of the muscularized diaphragm.

Indexed as

AnimalsConnective TissueDiaphragmDisease Models, AnimalGene Expression Regulation, DevelopmentalGenes, DevelopmentalMammalsMiceMice, Inbred C57BLMorphogenesisMuscle DevelopmentMuscle, SkeletalCDHCongenital Diaphragmatic HerniaDiaphragmMuscleSomite

Identifiers

PMID29679560
PMCPMC6089379
OpenAlexW2949919453

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.