Evidence map›Paper›PMID 38636516›Full record

ArticleDevelopmental cell2024

Mannose controls mesoderm specification and symmetry breaking in mouse gastruloids.

Chaitanya Dingare, Dominica Cao, Jenny Jingni Yang, Berna Sozen, Benjamin Steventon

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.5field-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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  4. Review
  5. Article
  6. N2B27 media formulations influence gastruloid development.Development (Cambridge, England) · 2025
    Article
  7. Article
  8. Article
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  12. Article
  13. Review
  14. Three-dimensional stem cell models of mammalian gastrulation.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
  15. Article
  16. Review
  17. Article
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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

5 authors at 3 institutions in 2 countries.

Chaitanya DingareDeptartment of Genetics, University of Cambridge, Downing Site, Cambridge CB2 3EH, UK. Electronic address: cd705@cam.ac.uk.
Dominica CaoDepartment of Genetics, Yale School of Medicine, Yale University, New Haven, CT, USA.
Jenny Jingni YangDeptartment of Genetics, University of Cambridge, Downing Site, Cambridge CB2 3EH, UK.
Berna SozenDepartment of Genetics, Yale School of Medicine, Yale University, New Haven, CT, USA; Yale Stem Cell Centre, Yale University, New Haven, CT, USA; Department of Obstetrics, Gynaecology and Reproductive Sciences, Yale School of Medicine, Yale University, New Haven, CT, USA.
Benjamin SteventonDeptartment of Genetics, University of Cambridge, Downing Site, Cambridge CB2 3EH, UK. Electronic address: bjs57@cam.ac.uk.
University of Cambridge · GBYale Cancer Center · USYale University · US

Funding

National Metabolomics Data Repository - nextgen Metabolomics WorkbenchU2CDK119886 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2018 to 2021
$12.7M
Biomedical Data Commons Workbench (BDCW)OT2OD030544 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2020 to 2024
$3.2M
NIDDK NIH HHS U2C DK119886NIH HHS OT2 OD030544Wellcome Trust 109408/Z/15/ZWellcome Trust 225360_Z_22_Z
6 · The paper itself

Abstract

Patterning and growth are fundamental features of embryonic development that must be tightly coordinated. To understand how metabolism impacts early mesoderm development, we used mouse embryonic stem-cell-derived gastruloids, that co-expressed glucose transporters with the mesodermal marker T/Bra. We found that the glucose mimic, 2-deoxy-D-glucose (2-DG), blocked T/Bra expression and abolished axial elongation in gastruloids. However, glucose removal did not phenocopy 2-DG treatment despite a decline in glycolytic intermediates. As 2-DG can also act as a competitive inhibitor of mannose in protein glycosylation, we added mannose together with 2-DG and found that it could rescue the mesoderm specification both in vivo and in vitro. We further showed that blocking production and intracellular recycling of mannose abrogated mesoderm specification. Proteomics analysis demonstrated that mannose reversed glycosylation of the Wnt pathway regulator, secreted frizzled receptor Frzb. Our study showed how mannose controls mesoderm specification in mouse gastruloids.

Indexed as

MannoseMesodermAnimalsBody PatterningCell DifferentiationDeoxyglucoseFrizzled ReceptorsGastrulaGene Expression Regulation, DevelopmentalGlycosylationMiceMouse Embryonic Stem CellsWnt Signaling PathwayDeoxyglucoseFrizzled ReceptorsMannoseFGFgastrulationgastruloidsglycosylationmetabolomicsself-organisationWnt

Identifiers

PMID38636516
PMCPMC7619011
OpenAlexW4394893773

What OpenQuestion holds

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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.