Evidence map›Paper›PMID 25631815›Full record

ArticleMolecular biology of the cell2015

Polarity protein Par3 controls B-cell receptor dynamics and antigen extraction at the immune synapse.

Anne Reversat, Maria-Isabel Yuseff, Danielle Lankar, Odile Malbec, Dorian Obino, Mathieu Maurin, Naga Venkata Gayathri Penmatcha, Alejandro Amoroso, Lucie Sengmanivong, Gregg G Gundersen and 5 more

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In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 41 citations in OpenAlex.

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  5. Positioning centrioles and centrosomes.The Journal of cell biology · 2024
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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

15 authors at 4 institutions in 3 countries.

Anne ReversatINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Maria-Isabel YuseffINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France Departamento de Biologia Celular y Molecular, Pontificia Universidad Catolica de Chile, 6513677 Santiago, Chile.
Danielle LankarINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Odile MalbecINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Dorian ObinoINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Mathieu MaurinINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Naga Venkata Gayathri PenmatchaINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Alejandro AmorosoINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France Facultad de Ciencias de la Salud, Universidad San Sebastián, 7510157 Santiago, Chile.
Lucie SengmanivongCell and Tissue Imaging Core Facility (PICT-IBiSA) and Nikon Imaging Centre, Institut Curie, UMR144, Centre de Recherche, 75005 Paris, France.
Gregg G GundersenDepartment of Pathology and Cell Biology, Columbia University, New York, NY 10032.
Ira MellmanGenentech, San Francisco, CA 94080.
François DarchenUniversité Paris Descartes, Sorbonne Paris Cité, CNRS UMR8250, 75270 Paris Cedex 06, France.
Claire DesnosUniversité Paris Descartes, Sorbonne Paris Cité, CNRS UMR8250, 75270 Paris Cedex 06, France.
Paolo PierobonINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Ana-Maria Lennon-DuménilINSERM U932, Institut Curie, Centre de Recherche, 75005 Paris, France.
Inserm · FRDélégation Paris 5 · FRBiologie cellulaire et Cancer · FRColumbia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B-cell receptor (BCR) engagement with surface-tethered antigens leads to the formation of an immune synapse, which facilitates antigen uptake for presentation to T-lymphocytes. Antigen internalization and processing rely on the early dynein-dependent transport of BCR-antigen microclusters to the synapse center, as well as on the later polarization of the microtubule-organizing center (MTOC). MTOC repositioning allows the release of proteases and the delivery of MHC class II molecules at the synapse. Whether and how these events are coordinated have not been addressed. Here we show that the ancestral polarity protein Par3 promotes BCR-antigen microcluster gathering, as well as MTOC polarization and lysosome exocytosis, at the synapse by facilitating local dynein recruitment. Par3 is also required for antigen presentation to T-lymphocytes. Par3 therefore emerges as a key molecule in the coupling of the early and late events needed for efficient extraction and processing of immobilized antigen by B-cells.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAntigen PresentationAntigensB-LymphocytesCell Adhesion MoleculesCell Cycle ProteinsImmunological SynapsesMiceReceptors, Antigen, B-CellAdaptor Proteins, Signal TransducingAntigensCell Adhesion MoleculesCell Cycle ProteinsPard3 protein, mouseReceptors, Antigen, B-Cell

Identifiers

PMID25631815
PMCPMC4454175
OpenAlexW2100427942

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.