Evidence map›Paper›PMID 21822214›Full record

ArticleThe EMBO journal2011

The B-cell antigen receptor signals through a preformed transducer module of SLP65 and CIN85.

Thomas Oellerich, Vanessa Bremes, Konstantin Neumann, Hanibal Bohnenberger, Kai Dittmann, He-Hsuan Hsiao, Michael Engelke, Tim Schnyder, Facundo D Batista, Henning Urlaub and 1 more

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. [Latest Findings on the Role of Liquid-Liquid Phase Separation in the Regulation of Immune Cell Activation and Key Signaling].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Phase separation in immune regulation and immune-related diseases.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  15. Review
  16. Phase separation in immune signalling.Nature reviews. Immunology · 2022
    Review
  17. Article
  18. Review
  19. 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

11 authors at 3 institutions in 2 countries.

Thomas OellerichInstitute of Cellular and Molecular Immunology, Georg-August-University Göttingen, Germany.
Vanessa Bremes
Konstantin Neumann
Hanibal Bohnenberger
Kai Dittmann
He-Hsuan Hsiao
Michael Engelke
Tim Schnyder
Facundo D Batista
Henning Urlaub
Jürgen Wienands
University of Göttingen · DECancer Research UK · GBMax Planck Institute for Biophysical Chemistry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spleen tyrosine kinase Syk and its substrate SLP65 (also called BLNK) are proximal signal transducer elements of the B-cell antigen receptor (BCR). Yet, our understanding of signal initiation and processing is limited owing to the incomplete list of SLP65 interaction partners and our ignorance of their association kinetics. We have now determined and quantified the in vivo interactomes of SLP65 in resting and stimulated B cells by mass spectrometry. SLP65 orchestrated a complex signal network of about 30 proteins that was predominantly based on dynamic interactions. However, a stimulation-independent and constant association of SLP65 with the Cbl-interacting protein of 85 kDa (CIN85) was requisite for SLP65 phosphorylation and its inducible plasma membrane translocation. In the absence of a steady SLP65/CIN85 complex, BCR-induced Ca(2+) and NF-κB responses were abrogated. Finally, live cell imaging and co-immunoprecipitation experiments further confirmed that both SLP65 and CIN85 are key components of the BCR-associated primary transducer module required for the onset and progression phases of BCR signal transduction.

Indexed as

Adaptor Proteins, Signal TransducingAmino Acid SequenceAnimalsB-LymphocytesCalciumHumansIntracellular Signaling Peptides and ProteinsMiceMolecular Sequence DataNeoplasm ProteinsNerve Tissue ProteinsNF-kappa BPhosphorylationProtein-Tyrosine KinasesReceptors, Antigen, B-CellSignal TransductionAdaptor Proteins, Signal TransducingB cell linker proteinCalciumIntracellular Signaling Peptides and ProteinsNeoplasm ProteinsNerve Tissue ProteinsNF-kappa BProtein-Tyrosine KinasesReceptors, Antigen, B-CellSH3KBP1 protein, humanSh3kbp1 protein, mouseSyk KinaseSYK protein, humanSyk protein, mouse

Identifiers

PMID21822214
PMCPMC3181483
OpenAlexW1854099023

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.