Evidence map›Paper›PMID 42477468›Full record

ArticleEMBO reports2026

Glycolytic suppression of cell adhesion promotes thyroid morphogenesis in response to nutrition.

Asako Shindo, Shiho Nishiguchi, Ayaka Fujiwara, Kaoru Nakashima

Abstract read
In one paragraph

Article in EMBO reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Asako ShindoDepartment of Biological Sciences, Graduate School of Science, The University of Osaka, Toyonaka, Japan. shindo.asako.sci@osaka-u.ac.jp.ORCID http://orcid.org/0000-0002-3314-7151
Shiho NishiguchiDepartment of Biological Sciences, Graduate School of Science, The University of Osaka, Toyonaka, Japan.
Ayaka FujiwaraInstitute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.
Kaoru NakashimaInstitute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.

Funding

Japan Agency for Medical Research and Development (AMED) 18068806MEXT | Japan Society for the Promotion of Science (JSPS) 21H05788MEXT | Japan Society for the Promotion of Science (JSPS) 22H05168MEXT | Japan Society for the Promotion of Science (JSPS) 23K18128MEXT | Japan Society for the Promotion of Science (JSPS) 24K02037MEXT | JST | Fusion Oriented REsearch for disruptive Science and Technology (FOREST) 21468158Yamada Science Foundation (YSF) NA
6 · The paper itself

Abstract

Organ morphogenesis relies on collective cellular behaviors. While intrinsic developmental programs governing cellular behaviors are well characterized, the effects of environmental and systemic factors on these behaviors remain poorly understood. Here, we investigate how nutritional availability modulates cellular behaviors during thyroid morphogenesis using Xenopus tadpoles as an in vivo model. RNA-seq analysis of thyroid regions from fed and unfed tadpoles shows that nutritional status alters gene expression profiles. We identify cell adhesion-related genes as key targets, with expression increased in unfed tadpoles and decreased in fed tadpoles. Immunostaining for E-cadherin supports the RNA-seq results, and functional inhibition of E-cadherin facilitates thyroid follicle formation. We further demonstrate that glycolytic activity reduces junctional E-cadherin accumulation in the thyroid, linking metabolism to the regulation of cell adhesion. Lastly, thyroid cells forming multi-luminal structures exhibit distinct apical-basal polarity, and these structures are enhanced by glycolytic activity and suppression of cell adhesion. These findings reveal a mechanism by which nutritional status remodels cellular properties underlying collective cellular behaviors during organ morphogenesis.

Indexed as

Cell AdhesionGlycolysisMorphogenesisThyroid GlandAnimalsCadherinsCell PolarityGene Expression Regulation, DevelopmentalLarvaNutritional StatusXenopus laevisCadherins

Identifiers

PMID42477468
PMCPMC13554297

What OpenQuestion holds

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Registered trials

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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.