Evidence map›Paper›PMID 36531949›Full record

ArticleFrontiers in cell and developmental biology2022

Mechano-biochemical marine stimulation of inversion, gastrulation, and endomesoderm specification in multicellular Eukaryota.

Ngoc Minh Nguyen, Tatiana Merle, Florence Broders-Bondon, Anne-Christine Brunet, Aude Battistella, Emelie Britt Linnea Land, Florian Sarron, Aditya Jha, Jean-Luc Gennisson, Eric Röttinger and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

12 authors at 1 institution in 1 country.

Ngoc Minh NguyenMechanics and Genetics of Embryonic Development Group, Institut Curie, Centre OCAV PSL Research University, CNRS, UMR168, Inserm, Sorbonne University, Paris, France.
Tatiana MerleMechanics and Genetics of Embryonic Development Group, Institut Curie, Centre OCAV PSL Research University, CNRS, UMR168, Inserm, Sorbonne University, Paris, France.
Florence Broders-BondonMechanics and Genetics of Embryonic Development Group, Institut Curie, Centre OCAV PSL Research University, CNRS, UMR168, Inserm, Sorbonne University, Paris, France.
Anne-Christine BrunetMechanics and Genetics of Embryonic Development Group, Institut Curie, Centre OCAV PSL Research University, CNRS, UMR168, Inserm, Sorbonne University, Paris, France.
Aude BattistellaBiochemistry, Molecular Biology, and Cells Platform, Institut Curie, CNRS, UMR 168, Inserm, Sorbonne University, Paris, France.
Emelie Britt Linnea LandMechanics and Genetics of Embryonic Development Group, Institut Curie, Centre OCAV PSL Research University, CNRS, UMR168, Inserm, Sorbonne University, Paris, France.
Florian SarronSorbonne Université, CNRS, UMR 7095, Institut d'Astrophysique de Paris, Paris, France.
Aditya JhaLaboratoire Physique et Mécanique des Milieux Hétérogènes (PMMH), CNRS, ESPCI ParisTech, Université Pierre et Marie Curie, Université Paris Diderot, Paris, France.
Jean-Luc GennissonUniversité Paris-Saclay, CEA, CNRS, Inserm, BioMaps, Service Hospitalier Frédéric Joliot, Orsay, France.
Eric RöttingerUniversité Côte d'Azur, CNRS, INSERM, Institute for Research on Cancer and Aging (IRCAN), Nice, France.
María Elena Fernández-SánchezMechanics and Genetics of Embryonic Development Group, Institut Curie, Centre OCAV PSL Research University, CNRS, UMR168, Inserm, Sorbonne University, Paris, France.
Emmanuel FargeMechanics and Genetics of Embryonic Development Group, Institut Curie, Centre OCAV PSL Research University, CNRS, UMR168, Inserm, Sorbonne University, Paris, France.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The evolutionary emergence of the primitive gut in Metazoa is one of the decisive events that conditioned the major evolutionary transition, leading to the origin of animal development. It is thought to have been induced by the specification of the endomesoderm (EM) into the multicellular tissue and its invagination (i.e., gastrulation). However, the biochemical signals underlying the evolutionary emergence of EM specification and gastrulation remain unknown. Herein, we find that hydrodynamic mechanical strains, reminiscent of soft marine flow, trigger active tissue invagination/gastrulation or curvature reversal

Indexed as

beta-catenin-dependent mechanosensitivitychoanoflagellate Choanoeca flexacnidaria Nematostella vectensisevolutionary emergence of first Metazoa organismshydrodynamic mechanical strainsmechanotransductionmyosin-dependent mechanosensitivityprimitive motor-sensorial behavioral mechanosensing

Identifiers

PMID36531949
PMCPMC9754125
OpenAlexW4311067436

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.