Evidence map›Paper›PMID 33667159›Full record

ArticleeLife2021

Retrograde ERK activation waves drive base-to-apex multicellular flow in murine cochlear duct morphogenesis.

Mamoru Ishii, Tomoko Tateya, Michiyuki Matsuda, Tsuyoshi Hirashima

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Wnt7b acts in concert with Wnt5a to regulate tissue elongation and planar cell polarity via noncanonical Wnt signaling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Emerging roles and mechanisms of ERK pathway mechanosensing.Cellular and molecular life sciences : CMLS · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Waves in Embryonic Development.Annual review of biophysics · 2022
    Review
  15. The mechanical forces that shape our senses.Development (Cambridge, England) · 2022
    Review
  16. Revealing epithelial morphogenetic mechanisms through live imaging.Current opinion in genetics & development · 2022
    Review
  17. Review
  18. Multiphoton intravital microscopy of rodents.Nature reviews. Methods primers · 2022
    Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Mamoru IshiiGraduate School of Biostudies, Kyoto University, Kyoto, Japan.
Tomoko TateyaDepartment of Speech and Hearing Sciences and Disorders, Faculty of Health and Medical Sciences, Kyoto University of Advanced Science, Kyoto, Japan.ORCID 0000-0002-0342-3688
Michiyuki MatsudaGraduate School of Biostudies, Kyoto University, Kyoto, Japan.ORCID 0000-0002-5876-9969
Tsuyoshi HirashimaGraduate School of Biostudies, Kyoto University, Kyoto, Japan.ORCID 0000-0001-7323-9627
Kyoto University · JPKyoto University of Advanced Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A notable example of spiral architecture in organs is the mammalian cochlear duct, where the morphology is critical for hearing function. Genetic studies have revealed necessary signaling molecules, but it remains unclear how cellular dynamics generate elongating, bending, and coiling of the cochlear duct. Here, we show that extracellular signal-regulated kinase (ERK) activation waves control collective cell migration during the murine cochlear duct development using deep tissue live-cell imaging, Förster resonance energy transfer (FRET)-based quantitation, and mathematical modeling. Long-term FRET imaging reveals that helical ERK activation propagates from the apex duct tip concomitant with the reverse multicellular flow on the lateral side of the developing cochlear duct, resulting in advection-based duct elongation. Moreover, model simulations, together with experiments, explain that the oscillatory wave trains of ERK activity and the cell flow are generated by mechanochemical feedback. Our findings propose a regulatory mechanism to coordinate the multicellular behaviors underlying the duct elongation during development.

Indexed as

Cell MovementMAP Kinase Signaling SystemAnimalsCochlear DuctEmbryo, MammalianFluorescence Resonance Energy TransferMiceMice, Inbred ICRMice, TransgenicModels, TheoreticalMorphogenesisdevelopmental biologyFRET imagingMAPK/ERKmathematical modelingmechano-chemical feedbacksmorphogenesismousemulticellular flow

Identifiers

PMID33667159
PMCPMC7935486
OpenAlexW3135505499

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.