Evidence map›Paper›PMID 31157616›Full record

ArticleeLife2019

Arp2/3 complex-driven spatial patterning of the BCR enhances immune synapse formation, BCR signaling and B cell activation.

Madison Bolger-Munro, Kate Choi, Joshua M Scurll, Libin Abraham, Rhys S Chappell, Duke Sheen, May Dang-Lawson, Xufeng Wu, John J Priatel, Daniel Coombs and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.4field-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

50 citing papers in PubMed, 73 citations in OpenAlex.

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  8. Antigen mobility regulates the dynamics and precision of antigen capture in the B cell immune synapse.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. The role of actin cytoskeleton component Arp2/3 in inflammatory response.Frontiers in cell and developmental biology · 2025
    Review
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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

12 authors at 2 institutions in 2 countries.

Madison Bolger-MunroDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.ORCID 0000-0002-8176-4824
Kate ChoiDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
Joshua M ScurllDepartment of Mathematics, Institute of Applied Mathematics, University of British Columbia, Vancouver, Canada.
Libin AbrahamDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
Rhys S ChappellDepartment of Mathematics, Institute of Applied Mathematics, University of British Columbia, Vancouver, Canada.
Duke SheenDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
May Dang-LawsonDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
Xufeng WuCell Biology and Physiology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, United States.
John J PriatelDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Daniel CoombsDepartment of Mathematics, Institute of Applied Mathematics, University of British Columbia, Vancouver, Canada.ORCID 0000-0002-8038-6278
John A HammerCell Biology and Physiology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, United States.
Michael R GoldDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.ORCID 0000-0003-1222-3191
University of British Columbia · CANational Institutes of Health · US

Funding

Roles of cytoskektal dynamics in T lymphocyte functionZIAHL006121 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HAMMER, JOHN A · 2011 to 2025
$19.8M
CIHR MOP-68865CIHR PJT-152946Natural Sciences and Engineering Research Council of Canada RGPIN-2015-04611
6 · The paper itself

Abstract

When B cells encounter antigens on the surface of an antigen-presenting cell (APC), B cell receptors (BCRs) are gathered into microclusters that recruit signaling enzymes. These microclusters then move centripetally and coalesce into the central supramolecular activation cluster of an immune synapse. The mechanisms controlling BCR organization during immune synapse formation, and how this impacts BCR signaling, are not fully understood. We show that this coalescence of BCR microclusters depends on the actin-related protein 2/3 (Arp2/3) complex, which nucleates branched actin networks. Moreover, in murine B cells, this dynamic spatial reorganization of BCR microclusters amplifies proximal BCR signaling reactions and enhances the ability of membrane-associated antigens to induce transcriptional responses and proliferation. Our finding that Arp2/3 complex activity is important for B cell responses to spatially restricted membrane-bound antigens, but not for soluble antigens, highlights a critical role for Arp2/3 complex-dependent actin remodeling in B cell responses to APC-bound antigens.

Indexed as

Lymphocyte ActivationSignal TransductionActin-Related Protein 3ActinsAngiopoietin-Like Protein 2Angiopoietin-like ProteinsAnimalsB-LymphocytesImmunological SynapsesMice, Inbred C57BLReceptors, Antigen, B-CellActin-Related Protein 3ActinsActr3 protein, mouseAngiopoietin-Like Protein 2Angiopoietin-like ProteinsAngptl2 protein, mouseReceptors, Antigen, B-Cellactin dynamicsantigen-presenting cellArp2/3 complexB cellB cell receptorcell biologyimmune synapseimmunologyinflammationmouse

Identifiers

PMID31157616
PMCPMC6591008
OpenAlexW2947462908

What OpenQuestion holds

Textmetadata
LicenceCC0
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.