Evidence map›Paper›PMID 36423208›Full record

ArticleJournal of anatomy2023

Sequential changes in cellular properties accompanying amniote somite formation.

Agnieszka M Piatkowska, Kaustubh Adhikari, Adam A Moverley, Mark Turmaine, James A Glazier, Nicolas Plachta, Susan E Evans, Claudio D Stern

Open access · hybridAbstract read
In one paragraph

Article in Journal of anatomy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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 2 countries.

Agnieszka M PiatkowskaDepartment of Cell & Developmental Biology, University College London, Gower Street (Anatomy Building), London, UK.
Kaustubh AdhikariDepartment of Cell & Developmental Biology, University College London, Gower Street (Anatomy Building), London, UK.
Adam A MoverleyDepartment of Cell & Developmental Biology, University College London, Gower Street (Anatomy Building), London, UK.
Mark TurmaineDepartment of Cell & Developmental Biology, University College London, Gower Street (Anatomy Building), London, UK.
James A GlazierDepartment of Intelligent Systems Engineering, Biocomplexity Institute, Bloomington, Indiana, USA.
Nicolas PlachtaDepartment of Cell and Developmental Biology, 9-123 Smilow Center for Translational Research, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-5035-7425
Susan E EvansDepartment of Cell & Developmental Biology, University College London, Gower Street (Anatomy Building), London, UK.ORCID 0000-0002-0799-4154
Claudio D SternDepartment of Cell & Developmental Biology, University College London, Gower Street (Anatomy Building), London, UK.ORCID 0000-0002-9907-889X
University College London · GBBiocom · USTranslational Therapeutics (United States) · US

Funding

MSM - Multiscale Studies of Segmentation in Vertebrate *R01GM076692 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI GLAZIER, JAMES ALEXANDER, STERN, CLAUDIO D · 2005 to 2015
$5.5M
Revealing how the mitotic spindle controls asymmetric cell division in vivoR01GM139970 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI PLACHTA, NICOLAS DANIEL · 2020 to 2023
$1.8M
Biotechnology and Biological Sciences Research Council BB/R003432/1NIGMS NIH HHS GM139970-01NIGMS NIH HHS R01GM076692Wellcome Trust 106044/Z/14/Z
6 · The paper itself

Abstract

Somites are transient structures derived from the pre-somitic mesoderm (PSM), involving mesenchyme-to-epithelial transition (MET) where the cells change their shape and polarize. Using Scanning electron microscopy (SEM), immunocytochemistry and confocal microscopy, we study the progression of these events along the tail-to-head axis of the embryo, which mirrors the progression of somitogenesis (younger cells located more caudally). SEM revealed that PSM epithelialization is a gradual process, which begins much earlier than previously thought, starting with the dorsalmost cells, then the medial ones, and then, simultaneously, the ventral and lateral cells, before a somite fully separates from the PSM. The core (internal) cells of the PSM and somites never epithelialize, which suggests that the core cells could be 'trapped' within the somitocoele after cells at the surfaces of the PSM undergo MET. Three-dimensional imaging of the distribution of the cell polarity markers PKCζ, PAR3, ZO1, the Golgi marker GM130 and the apical marker N-cadherin reveal that the pattern of polarization is distinctive for each marker and for each surface of the PSM, but the order of these events is not the same as the progression of cell elongation. These observations challenge some assumptions underlying existing models of somite formation.

Indexed as

MesodermSomitesCadherinsEmbryonic DevelopmentMorphogenesisCadherinscell adhesioncell polarityepithelial-mesenchymal transitionmesenchymal-epithelial transitionsegmentationvertebral column

Identifiers

PMID36423208
PMCPMC9919497
OpenAlexW4309918633

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.