Evidence map›Paper›PMID 25941375›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Single-cell mass spectrometry reveals small molecules that affect cell fates in the 16-cell embryo.

Rosemary M Onjiko, Sally A Moody, Peter Nemes

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

102 citing papers in PubMed, 192 citations in OpenAlex.

  1. Trial
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  6. Technologies for Decoding Cancer Metabolism with Spatial Resolution.Cold Spring Harbor perspectives in medicine · 2025
    Review
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  11. Cell lineage-guided mass spectrometry reveals increased energy metabolism and reactive oxygen species in the vertebrate organizer.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Top-down proteomics.Nature reviews. Methods primers · 2024
    Article
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  16. Article
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  18. Review
  19. Article
  20. Article

42 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Rosemary M OnjikoDepartment of Chemistry, W. M. Keck Institute for Proteomics Technology and Applications, The George Washington University, Washington, DC 20052; and.
Sally A MoodyDepartment of Anatomy and Regenerative Biology, School of Medicine and Health Sciences, The George Washington University, Washington, DC 20037.
Peter NemesDepartment of Chemistry, W. M. Keck Institute for Proteomics Technology and Applications, The George Washington University, Washington, DC 20052; and petern@gwu.edu.
George Washington University · USW. M. Keck Foundation · US

Funding

In Situ Optoguided Microsampling Single-cell Mass Spectrometry for Elucidating Cell HeterogeneityR21GM114854 · NIGMS · GEORGE WASHINGTON UNIVERSITY · PI NEMES, PETER · 2014 to 2015
$361k
NIGMS NIH HHS R21 GM114854
6 · The paper itself

Abstract

Spatial and temporal changes in molecular expression are essential to embryonic development, and their characterization is critical to understand mechanisms by which cells acquire different phenotypes. Although technological advances have made it possible to quantify expression of large molecules during embryogenesis, little information is available on metabolites, the ultimate indicator of physiological activity of the cell. Here, we demonstrate that single-cell capillary electrophoresis-electrospray ionization mass spectrometry is able to test whether differential expression of the genome translates to the domain of metabolites between single embryonic cells. Dissection of three different cell types with distinct tissue fates from 16-cell embryos of the South African clawed frog (Xenopus laevis) and microextraction of their metabolomes enabled the identification of 40 metabolites that anchored interconnected central metabolic networks. Relative quantitation revealed that several metabolites were differentially active between the cell types in the wild-type, unperturbed embryos. Altering postfertilization cytoplasmic movements that perturb dorsal development confirmed that these three cells have characteristic small-molecular activity already at cleavage stages as a result of cell type and not differences in pigmentation, yolk content, cell size, or position in the embryo. Changing the metabolite concentration caused changes in cell movements at gastrulation that also altered the tissue fates of these cells, demonstrating that the metabolome affects cell phenotypes in the embryo.

Indexed as

AnimalsBlastomeresCell SizeElectrophoresis, CapillaryEmbryo, NonmammalianFemaleMaleMetabolic Networks and PathwaysMetabolomeSingle-Cell AnalysisSpectrometry, Mass, Electrospray IonizationXenopus laevisembryo developmentmass spectrometrymetabolomicssingle cellXenopus

Identifiers

PMID25941375
PMCPMC4450407
OpenAlexW1586577995

What OpenQuestion holds

Textmetadata
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.