Evidence map›Paper›PMID 24130328›Full record

ArticleDevelopment (Cambridge, England)2013

Derivation of lung mesenchymal lineages from the fetal mesothelium requires hedgehog signaling for mesothelial cell entry.

Radhika Dixit, Xingbin Ai, Alan Fine

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
–field-weighted citation impact
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

66 citing papers in PubMed.

  1. Article
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  3. Review
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  8. Review
  9. Article
  10. Article
  11. Article
  12. Understanding myofibroblast origin in the fibrotic lung.Chinese medical journal pulmonary and critical care medicine · 2024
    Review
  13. Article
  14. Nephronectin is required to maintain right lung lobar separation during embryonic development.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

6 more citing papers are in PubMed but not listed here.

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.

Radhika DixitThe Pulmonary Center, Department of Medicine, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA.
Xingbin Ai
Alan Fine

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
The Fetal Lung Mesothelial Differentiation ProgramR01HL116163 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI AI, XINGBIN, FINE, ALAN FINE · 2013 to 2016
$2.3M
Identifying Molecular Phenotype of Normal and Asthmatic Bronchial Smooth MuscleR21HL112619 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI AI, XINGBIN, FINE, ALAN FINE · 2012 to 2013
$440k
CELLULAR AND INTERSTITIAL EDEMA DURING SURGICAL STRESSESF32HL008574 · NHLBI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI MOON, PAULA F · 1991 to 1993
–
NHLBI NIH HHS 1R01HL116163NHLBI NIH HHS 1R21HL112619NHLBI NIH HHS HL08574NHLBI NIH HHS R01 HL116163NHLBI NIH HHS R21 HL112619NIH HHS OD011107NIH HHS P51 OD011107
6 · The paper itself

Abstract

Recent studies have shown that mesothelial progenitors contribute to mesenchymal lineages of developing organs. To what extent the overlying mesothelium contributes to lung development remains unknown. To rigorously address this question, we employed Wt1(CreERT2/+) mice for high-fidelity lineage tracing after confirming that Cre recombinase was mesothelial specific and faithfully recapitulated endogenous Wilms' tumor 1 (Wt1) gene expression. We visualized WT1(+) mesothelial cell entry into the lung by live imaging and identified their progenies in subpopulations of bronchial smooth muscle cells, vascular smooth muscle cells and desmin(+) fibroblasts by lineage tagging. Derivation of these lineages was only observed with Cre recombinase activation during early lung development. Using loss-of-function assays in organ cultures, and targeted mesothelial-restricted hedgehog loss-of-function mice, we demonstrated that mesothelial cell movement into the lung requires the direct action of hedgehog signaling. By contrast, hedgehog signaling was not required for fetal mesothelial heart entry. These findings further support a paradigm wherein the mesothelium is a source of progenitors for mesenchymal lineages during organogenesis and indicate that signals controlling mesothelial cell entry are organ specific.

Indexed as

Animalsbeta-GalactosidaseCell LineageDNA PrimersFetusHedgehog ProteinsImmunohistochemistryIn Situ HybridizationIntegrasesLungMesodermMiceMice, TransgenicReverse Transcriptase Polymerase Chain ReactionSignal TransductionTime-Lapse Imagingbeta-GalactosidaseCre recombinaseDNA PrimersHedgehog ProteinsIntegrasesWT1 ProteinsHedgehog (Hh)Lung mesenchymeMesotheliumMouse

Identifiers

PMID24130328
PMCPMC4007715

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.