Evidence map›Paper›PMID 22400492›Full record

ArticleAnalytical chemistry2012

Metabolic cytometry: capillary electrophoresis with two-color fluorescence detection for the simultaneous study of two glycosphingolipid metabolic pathways in single primary neurons.

David C Essaka, Jillian Prendergast, Richard B Keithley, Monica M Palcic, Ole Hindsgaul, Ronald L Schnaar, Norman J Dovichi

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Analytical chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
7.3field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Analytical Techniques for Single-Cell Biochemical Assays of Lipids.Annual review of biomedical engineering · 2023
    Review
  3. Article
  4. Article
  5. Preserving Single Cells in Space and Time for Analytical Assays.Trends in analytical chemistry : TRAC · 2020
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Analysis of sphingosine kinase activity in single natural killer cells from peripheral blood.Integrative biology : quantitative biosciences from nano to macro · 2015
    Article
  12. Article
  13. Small-volume analysis of cell-cell signaling molecules in the brain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    Review
  14. Article
  15. Article
  16. Progress toward single cell metabolomics.Current opinion in biotechnology · 2013
    Review
  17. Article
  18. Separation of fluorescently labeled phosphoinositides and sphingolipids by capillary electrophoresis.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2012
    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

7 authors at 4 institutions in 2 countries.

David C EssakaDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, United States.
Jillian Prendergast
Richard B Keithley
Monica M Palcic
Ole Hindsgaul
Ronald L Schnaar
Norman J Dovichi
Carlsberg Laboratory · DKJohns Hopkins University · USUniversity of Notre Dame · USUniversity of Washington · US

Funding

Glycolipid metabolism in single cellsR01NS061767 · NINDS · UNIVERSITY OF WASHINGTON · PI DOVICHI, NORMAN J · 2007 to 2011
$1.8M
NINDS NIH HHS R01 NS061767NINDS NIH HHS R01NS061767
6 · The paper itself

Abstract

Metabolic cytometry is a form of chemical cytometry wherein metabolic cascades are monitored in single cells. We report the first example of metabolic cytometry where two different metabolic pathways are simultaneously monitored. Glycolipid catabolism in primary rat cerebella neurons was probed by incubation with tetramethylrhodamine-labeled GM1 (GM1-TMR). Simultaneously, both catabolism and anabolism were probed by coincubation with BODIPY-FL labeled LacCer (LacCer-BODIPY-FL). In a metabolic cytometry experiment, single cells were incubated with substrate, washed, aspirated into a capillary, and lysed. The components were separated by capillary electrophoresis equipped with a two-spectral channel laser-induced fluorescence detector. One channel monitored fluorescence generated by the metabolic products produced from GM1-TMR and the other monitored the metabolic products produced from LacCer-BODIPY-FL. The metabolic products were identified by comparison with the mobility of a set of standards. The detection system produced at least 6 orders of magnitude dynamic range in each spectral channel with negligible spectral crosstalk. Detection limits were 1 zmol for BODIPY-FL and 500 ymol for tetramethylrhodamine standard solutions.

Indexed as

AnimalsBoron CompoundsBrainCells, CulturedElectrophoresis, CapillaryEquipment DesignFluorescenceFluorescent DyesGlycosphingolipidsLactosylceramidesLimit of DetectionMetabolic Networks and PathwaysMicroscopy, FluorescenceNeuronsRatsRhodamines4,4-difluoro-4-bora-3a,4a-diaza-s-indaceneBODIPY-LacCerBoron CompoundsFluorescent DyesGlycosphingolipidsLactosylceramidesRhodaminestetramethylrhodamine

Identifiers

PMID22400492
PMCPMC3313455
OpenAlexW2034787930

What OpenQuestion holds

Textmetadata
LicenceTDM
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.