Evidence map›Paper›PMID 22265688›Full record

ArticleFEBS letters2012

Single-particle tracking of immunoglobulin E receptors (FcεRI) in micron-sized clusters and receptor patches.

Kathrin Spendier, Keith A Lidke, Diane S Lidke, James L Thomas

Abstract read
In one paragraph

Article in FEBS letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  16. Intracellular tracking of single-plasmid DNA particles after delivery by electroporation.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    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

4 authors.

Kathrin SpendierDepartment of Physics and Astronomy, University of New Mexico, Albuquerque, NM 87131, USA.
Keith A Lidke
Diane S Lidke
James L Thomas

Funding

UNM TRAININGP50GM085273 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI EDWARDS, JEREMY S · 2009 to 2018
$26.1M
Integrated, Interdisciplinary, Inter-university PHD Program Computational BiologyT32EB009414 · NIBIB · UNIVERSITY OF NEW MEXICO · PI SMITH, FELISA ANNAMARIE · 2009 to 2013
$989k
NIBIB NIH HHS T32 EB009414NIBIB NIH HHS T32EB009414NIGMS NIH HHS P50 GM085273NIGMS NIH HHS P50GM085273
6 · The paper itself

Abstract

When mast cells contact a monovalent antigen-bearing fluid lipid bilayer, IgE-loaded FcεRI receptors aggregate at contact points and trigger degranulation and the release of immune activators. We used two-color total internal reflection fluorescence microscopy and single-particle tracking to show that most fluorescently labeled receptor complexes diffuse freely within these micron-size clusters, with a diffusion coefficient comparable to free receptors in resting cells. At later times, when the small clusters coalesce to form larger patches, receptors diffuse even more rapidly. In all cases, Monte Carlo diffusion simulations ensured that the tracking results were free of bias, and distinguished biological from statistical variation. These results show the diversity in receptor mobility in mast cells, demonstrating at least three distinct states of receptor diffusivity.

Indexed as

AnimalsCell DegranulationCell LineDiffusionFluorescent DyesImmunoglobulin ELipid BilayersMast CellsMicroscopy, FluorescenceMonte Carlo MethodRatsReceptor AggregationReceptors, IgESignal TransductionFluorescent DyesImmunoglobulin ELipid BilayersReceptors, IgE

Identifiers

PMID22265688
PMCPMC3413461

What OpenQuestion holds

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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.