Evidence map›Paper›PMID 31974357›Full record

ArticleNature communications2020

WASP family proteins regulate the mobility of the B cell receptor during signaling activation.

Ivan Rey-Suarez, Brittany A Wheatley, Peter Koo, Anshuman Bhanja, Zhou Shu, Simon Mochrie, Wenxia Song, Hari Shroff, Arpita Upadhyaya

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 44 citations in OpenAlex.

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  6. The role of actin cytoskeleton component Arp2/3 in inflammatory response.Frontiers in cell and developmental biology · 2025
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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

9 authors at 6 institutions in 2 countries.

Ivan Rey-SuarezBiophysics Program, University of Maryland, College Park, MD, 20742, USA.
Brittany A WheatleyDepartment of Physics, University of Maryland, College Park, MD, 20742, USA.
Peter KooDepartment of Molecular & Cellular Biology, Harvard University, Cambridge, MA, 02138, USA.
Anshuman BhanjaDepartment of Cell Biology & Molecular Genetics, University of Maryland, College Park, MD, 20742, USA.
Zhou ShuDepartment of Cell Biology & Molecular Genetics, University of Maryland, College Park, MD, 20742, USA.
Simon MochrieDepartment of Physics, Yale University, New Haven, CT, 06520, USA.
Wenxia SongDepartment of Cell Biology & Molecular Genetics, University of Maryland, College Park, MD, 20742, USA.
Hari ShroffNational Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD, USA.
Arpita UpadhyayaBiophysics Program, University of Maryland, College Park, MD, 20742, USA. arpitau@umd.edu.
University of Maryland, College Park · USChongqing Medical University · CNHarvard University · USNational Institute of Biomedical Imaging and Bioengineering · USNational Institutes of Health · USYale University · US

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
Section on High Resolution Optical ImagingZIAEB000074 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI SHROFF, HARI · 2010 to 2022
$15.2M
Nanotopographic modulation of B cell signaling activationR21AI122205 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI UPADHYAYA, ARPITA · 2016 to 2017
$413k
NCI NIH HHS P30 CA045508NIAID NIH HHS R21 AI122205
6 · The paper itself

Abstract

Regulation of membrane receptor mobility tunes cellular response to external signals, such as in binding of B cell receptors (BCR) to antigen, which initiates signaling. However, whether BCR signaling is regulated by BCR mobility, and what factors mediate this regulation, are not well understood. Here we use single molecule imaging to examine BCR movement during signaling activation and a novel machine learning method to classify BCR trajectories into distinct diffusive states. Inhibition of actin dynamics downstream of the actin nucleating factors, Arp2/3 and formin, decreases BCR mobility. Constitutive loss or acute inhibition of the Arp2/3 regulator, N-WASP, which is associated with enhanced signaling, increases the proportion of BCR trajectories with lower diffusivity. Furthermore, loss of N-WASP reduces the diffusivity of CD19, a stimulatory co-receptor, but not that of FcγRIIB, an inhibitory co-receptor. Our results implicate a dynamic actin network in fine-tuning receptor mobility and receptor-ligand interactions for modulating B cell signaling.

Indexed as

Actin-Related Protein 2-3 ComplexActinsAnimalsAntigens, CD19B-LymphocytesMice, Inbred C57BLMice, KnockoutMice, TransgenicReceptors, Antigen, B-CellReceptors, IgGSignal TransductionSingle Molecule ImagingWiskott-Aldrich Syndrome Protein FamilyWiskott-Aldrich Syndrome Protein, NeuronalActin-Related Protein 2-3 ComplexActinsAntigens, CD19CD19 antigen, mouseFcgr2b protein, mouseReceptors, Antigen, B-CellReceptors, IgGWasl protein, mouseWiskott-Aldrich Syndrome Protein FamilyWiskott-Aldrich Syndrome Protein, Neuronal

Identifiers

PMID31974357
PMCPMC6978525
OpenAlexW3000982459

What OpenQuestion holds

Textmetadata
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.