Evidence map›Paper›PMID 24559180›Full record

ArticleAnalytical chemistry2014

Patch clamp electrophysiology and capillary electrophoresis-mass spectrometry metabolomics for single cell characterization.

Jordan T Aerts, Kathleen R Louis, Shane R Crandall, Gubbi Govindaiah, Charles L Cox, Jonathan V Sweedler

Open access · bronzeAbstract read
In one paragraph

Article in Analytical chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
6.3field-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

60 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
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  10. Article
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  13. Single cell metabolism: current and future trends.Metabolomics : Official journal of the Metabolomic Society · 2022
    Review
  14. Article
  15. The Intriguing Landscape of Single-Cell Protein Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Advanced tools and methods for single-cell surgery.Microsystems & nanoengineering · 2022
    Review
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

6 authors at 2 institutions in 1 country.

Jordan T AertsBeckman Institute for Advanced Science and Technology, ‡Department of Pharmacology, §Department of Molecular and Integrative Physiology, ∥Department of Chemistry, and ⊥Neuroscience Program, University of Illinois at Urbana-Champaign , Urbana, Illinois 61801, United States.
Kathleen R Louis
Shane R Crandall
Gubbi Govindaiah
Charles L Cox
Jonathan V Sweedler
University of Illinois Urbana-Champaign · USMichigan State University · US

Funding

The UIUC Neuroproteomics Center on Cell-Cell SignalingP30DA018310 · NIDA · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI Jonathan V. Sweedler · 2004 to 2026
$24.9M
Modulation of Subcortical Visual Information ProcessingR01EY014024 · NEI · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI COX, CHARLES LEROY · 2003 to 2012
$2.6M
Synaptic Phenotype, Development, and Plasticity in the Fragile X MouseR01MH085324 · NIMH · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI COX, CHARLES LEROY · 2010 to 2015
$2.1M
Glia classification via single cell metabolomicsR21MH100704 · NIMH · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI RUBAKHIN, STANISLAV S., SWEEDLER, JONATHAN V. · 2013 to 2014
$419k
Functions of naturally diverse inhibitory networks in neocortexF32NS084763 · NINDS · BROWN UNIVERSITY · PI CRANDALL, SHANE R · 2013 to 2015
$159k
NEI NIH HHS R01 EY014024NIDA NIH HHS P30 DA018310NIMH NIH HHS R01 MH085324NIMH NIH HHS R21 MH100704NINDS NIH HHS F32 NS084763
6 · The paper itself

Abstract

The visual selection of specific cells within an ex vivo brain slice, combined with whole-cell patch clamp recording and capillary electrophoresis (CE)-mass spectrometry (MS)-based metabolomics, yields high chemical information on the selected cells. By providing access to a cell's intracellular environment, the whole-cell patch clamp technique allows one to record the cell's physiological activity. A patch clamp pipet is used to withdraw ∼3 pL of cytoplasm for metabolomic analysis using CE-MS. Sampling the cytoplasm, rather than an intact isolated neuron, ensures that the sample arises from the cell of interest and that structures such as presynaptic terminals from surrounding, nontargeted neurons are not sampled. We sampled the rat thalamus, a well-defined system containing gamma-aminobutyric acid (GABA)-ergic and glutamatergic neurons. The approach was validated by recording and sampling from glutamatergic thalamocortical neurons, which receive major synaptic input from GABAergic thalamic reticular nucleus neurons, as well as neurons and astrocytes from the ventral basal nucleus and the dorsal lateral geniculate nucleus. From the analysis of the cytoplasm of glutamatergic cells, approximately 60 metabolites were detected, none of which corresponded to the compound GABA. However, GABA was successfully detected when sampling the cytoplasm of GABAergic neurons, demonstrating the exclusive nature of our cytoplasmic sampling approach. The combination of whole-cell patch clamp with single cell cytoplasm metabolomics provides the ability to link the physiological activity of neurons and astrocytes with their neurochemical state. The observed differences in the metabolome of these neurons underscore the striking cell to cell heterogeneity in the brain.

Indexed as

MetabolomicsPatch-Clamp TechniquesElectrophoresis, CapillaryMass Spectrometry

Identifiers

PMID24559180
PMCPMC3964733
OpenAlexW2026702694

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.