Evidence map›Paper›PMID 26104298›Full record

ArticleNature communications2015

Digital microfluidic immunocytochemistry in single cells.

Alphonsus H C Ng, M Dean Chamberlain, Haozhong Situ, Victor Lee, Aaron R Wheeler

Abstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Analytical chemistry · 2024
    Article
  5. On-chip dielectrophoretic single-cell manipulation.Microsystems & nanoengineering · 2024
    Review
  6. Review
  7. Article
  8. Beyond single cells: microfluidics empowering multiomics analysis.Analytical and bioanalytical chemistry · 2024
    Review
  9. Article
  10. Article
  11. The Intriguing Landscape of Single-Cell Protein Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Profiling Cell Signaling Networks at Single-cell Resolution.Molecular & cellular proteomics : MCP · 2020
    Review
  17. Article
  18. Article
  19. In Situ Single-Cell Western Blot on Adherent Cell Culture.Angewandte Chemie (International ed. in English) · 2019
    Review
  20. 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

5 authors.

Alphonsus H C NgInstitute of Biomaterials and Biomedical Engineering, University of Toronto, 164 College Street, Toronto, Ontario M5S 3G9, Canada.
M Dean ChamberlainInstitute of Biomaterials and Biomedical Engineering, University of Toronto, 164 College Street, Toronto, Ontario M5S 3G9, Canada.
Haozhong SituInstitute of Biomaterials and Biomedical Engineering, University of Toronto, 164 College Street, Toronto, Ontario M5S 3G9, Canada.
Victor LeeDonnelly Centre for Cellular and Biomolecular Research, 160 College Street, Toronto, Ontario M5S 3E1, Canada.
Aaron R WheelerInstitute of Biomaterials and Biomedical Engineering, University of Toronto, 164 College Street, Toronto, Ontario M5S 3G9, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a new technique called Digital microfluidic Immunocytochemistry in Single Cells (DISC). DISC automates protocols for cell culture, stimulation and immunocytochemistry, enabling the interrogation of protein phosphorylation on pulsing with stimulus for as little as 3 s. DISC was used to probe the phosphorylation states of platelet-derived growth factor receptor (PDGFR) and the downstream signalling protein, Akt, to evaluate concentration- and time-dependent effects of stimulation. The high time resolution of the technique allowed for surprising new observations-for example, a 10 s pulse stimulus of a low concentration of PDGF is sufficient to cause >30% of adherent fibroblasts to commit to Akt activation. With the ability to quantitatively probe signalling events with high time resolution at the single-cell level, we propose that DISC may be an important new technique for a wide range of applications, especially for screening signalling responses of a heterogeneous cell population.

Indexed as

MicrofluidicsAnimalsCell Culture TechniquesCell LineFibroblastsHumansImmunohistochemistryMCF-7 CellsMiceMicrofluidic Analytical TechniquesNIH 3T3 CellsPhosphorylationPlatelet-Derived Growth FactorProto-Oncogene Proteins c-aktSignal TransductionPlatelet-Derived Growth FactorProto-Oncogene Proteins c-akt

Identifiers

PMID26104298
PMCPMC4491823

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.