Evidence map›Paper›PMID 26671981›Full record

ArticleThe EMBO journal2016

Nanoscale organization and dynamics of the siglec CD22 cooperate with the cytoskeleton in restraining BCR signalling.

Francesca Gasparrini, Christoph Feest, Andreas Bruckbauer, Pieta K Mattila, Jennifer Müller, Lars Nitschke, Dennis Bray, Facundo D Batista

Abstract read
In one paragraph

Article in The EMBO journal, 2016. 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
–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

60 citing papers in PubMed.

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  18. The role ofFrontiers in immunology · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Francesca GasparriniLincoln's Inn Fields Laboratory, The Francis Crick Institute, London, UK.
Christoph FeestLincoln's Inn Fields Laboratory, The Francis Crick Institute, London, UK.
Andreas BruckbauerLincoln's Inn Fields Laboratory, The Francis Crick Institute, London, UK.
Pieta K MattilaLincoln's Inn Fields Laboratory, The Francis Crick Institute, London, UK.
Jennifer MüllerChair of Genetics, Department of Biology, University of Erlangen, Erlangen, Germany.
Lars NitschkeChair of Genetics, Department of Biology, University of Erlangen, Erlangen, Germany.
Dennis BrayDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Facundo D BatistaLincoln's Inn Fields Laboratory, The Francis Crick Institute, London, UK facundo.batista@crick.ac.uk.

Funding

Cancer Research UK
6 · The paper itself

Abstract

Receptor organization and dynamics at the cell membrane are important factors of signal transduction regulation. Using super-resolution microscopy and single-particle tracking, we show how the negative coreceptor CD22 works with the cortical cytoskeleton in restraining BCR signalling. In naïve B cells, we found endogenous CD22 to be highly mobile and organized into nanodomains. The landscape of CD22 and its lateral diffusion were perturbed either in the absence of CD45 or when the CD22 lectin domain was mutated. To understand how a relatively low number of CD22 molecules can keep BCR signalling in check, we generated Brownian dynamic simulations and supported them with ex vivo experiments. This combined approach suggests that the inhibitory function of CD22 is influenced by its nanoscale organization and is ensured by its fast diffusion enabling a "global BCR surveillance" at the plasma membrane.

Indexed as

Signal TransductionAnimalsB-LymphocytesCytoskeletonMice, Inbred BALB CMice, Inbred C57BLMicroscopy, FluorescenceReceptors, Antigen, B-CellSialic Acid Binding Ig-like Lectin 2Cd22 protein, mouseReceptors, Antigen, B-CellSialic Acid Binding Ig-like Lectin 2B‐cell receptor signallingglycoprotein CD45membrane dynamicssiglec CD22super‐resolution microscopy

Identifiers

PMID26671981
PMCPMC4741297

What Socratic 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 Socratic graph.