Evidence map›Paper›PMID 30026494›Full record

ArticleNature communications2018

Synchronized mesenchymal cell polarization and differentiation shape the formation of the murine trachea and esophagus.

Keishi Kishimoto, Masaru Tamura, Michiru Nishita, Yasuhiro Minami, Akira Yamaoka, Takaya Abe, Mayo Shigeta, Mitsuru Morimoto

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.8field-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

44 citing papers in PubMed, 75 citations in OpenAlex.

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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.

Keishi KishimotoLaboratory for Lung Development, RIKEN Center for Developmental Biology, Kobe, 650-0047, Japan.ORCID http://orcid.org/0000-0002-2938-1754
Masaru TamuraRIKEN BioResource Center, Tsukuba, Ibaraki, 305-0074, Japan.ORCID http://orcid.org/0000-0002-0311-8827
Michiru NishitaDivision of Cell Physiology, Department of Physiology and Cell Biology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Yasuhiro MinamiDivision of Cell Physiology, Department of Physiology and Cell Biology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Akira YamaokaLaboratory for Lung Development, RIKEN Center for Developmental Biology, Kobe, 650-0047, Japan.ORCID http://orcid.org/0000-0002-8629-5406
Takaya AbeCenter for Biosystems Dynamics Research, Kobe, 650-0047, Japan.
Mayo ShigetaCenter for Biosystems Dynamics Research, Kobe, 650-0047, Japan.
Mitsuru MorimotoLaboratory for Lung Development, RIKEN Center for Developmental Biology, Kobe, 650-0047, Japan. mitsuru.morimoto@riken.jp.ORCID http://orcid.org/0000-0001-9132-4155
RIKEN Center for Biosystems Dynamics Research · JPKobe University · JPRIKEN BioResource Research Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tube morphogenesis is essential for internal-organ development, yet the mechanisms regulating tube shape remain unknown. Here, we show that different mechanisms regulate the length and diameter of the murine trachea. First, we found that trachea development progresses via sequential elongation and expansion processes. This starts with a synchronized radial polarization of smooth muscle (SM) progenitor cells with inward Golgi-apparatus displacement regulates tube elongation, controlled by mesenchymal Wnt5a-Ror2 signaling. This radial polarization directs SM progenitor cell migration toward the epithelium, and the resulting subepithelial morphogenesis supports tube elongation to the anteroposterior axis. This radial polarization also regulates esophageal elongation. Subsequently, cartilage development helps expand the tube diameter, which drives epithelial-cell reshaping to determine the optimal lumen shape for efficient respiration. These findings suggest a strategy in which straight-organ tubulogenesis is driven by subepithelial cell polarization and ring cartilage development.

Indexed as

Actin CytoskeletonAnimalsCartilageCell DifferentiationCell PolarityEmbryo, MammalianEsophagusFemaleForkhead Transcription FactorsGene Expression Regulation, DevelopmentalGolgi ApparatusMaleMesenchymal Stem CellsMiceMice, TransgenicMorphogenesisForkhead Transcription FactorsFoxg1 protein, mouseNerve Tissue ProteinsReceptor Tyrosine Kinase-like Orphan ReceptorsRor2 protein, mouseSox9 protein, mouseSOX9 Transcription FactorWnt-5a ProteinWnt5a protein, mouse

Identifiers

PMID30026494
PMCPMC6053463
OpenAlexW2950627486

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.