Evidence map›Paper›PMID 27154205›Full record

ArticleThe EMBO journal2016

Rac1-Rab11-FIP3 regulatory hub coordinates vesicle traffic with actin remodeling and T-cell activation.

Jérôme Bouchet, Iratxe Del Río-Iñiguez, Rémi Lasserre, Sonia Agüera-Gonzalez, Céline Cuche, Anne Danckaert, Mary W McCaffrey, Vincenzo Di Bartolo, Andrés Alcover

Open access · greenAbstract 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 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

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  20. Multifaceted Rho GTPase Signaling at the Endomembranes.Frontiers in cell and developmental biology · 2019
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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 3 institutions in 2 countries.

Jérôme BouchetLymphocyte Cell Biology Unit, Department of Immunology, Institut Pasteur, Paris, France CNRS URA 1961, Paris, France INSERM U1221, Paris, France jerome.bouchet@inserm.fr andres.alcover@pasteur.fr.ORCID 0000-0002-6611-4380
Iratxe Del Río-IñiguezLymphocyte Cell Biology Unit, Department of Immunology, Institut Pasteur, Paris, France CNRS URA 1961, Paris, France INSERM U1221, Paris, France.
Rémi LasserreLymphocyte Cell Biology Unit, Department of Immunology, Institut Pasteur, Paris, France CNRS URA 1961, Paris, France.
Sonia Agüera-GonzalezLymphocyte Cell Biology Unit, Department of Immunology, Institut Pasteur, Paris, France CNRS URA 1961, Paris, France.
Céline CucheLymphocyte Cell Biology Unit, Department of Immunology, Institut Pasteur, Paris, France CNRS URA 1961, Paris, France INSERM U1221, Paris, France.
Anne DanckaertInstitut Pasteur Citech-Imagopole, Paris, France.
Mary W McCaffreyMolecular Cell Biology Laboratory, Biosciences Institute, School of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.
Vincenzo Di BartoloLymphocyte Cell Biology Unit, Department of Immunology, Institut Pasteur, Paris, France CNRS URA 1961, Paris, France INSERM U1221, Paris, France.
Andrés AlcoverLymphocyte Cell Biology Unit, Department of Immunology, Institut Pasteur, Paris, France CNRS URA 1961, Paris, France INSERM U1221, Paris, France jerome.bouchet@inserm.fr andres.alcover@pasteur.fr.ORCID 0000-0002-9507-3450
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRUniversity College Cork · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immunological synapse generation and function is the result of a T-cell polarization process that depends on the orchestrated action of the actin and microtubule cytoskeleton and of intracellular vesicle traffic. However, how these events are coordinated is ill defined. Since Rab and Rho families of GTPases control intracellular vesicle traffic and cytoskeleton reorganization, respectively, we investigated their possible interplay. We show here that a significant fraction of Rac1 is associated with Rab11-positive recycling endosomes. Moreover, the Rab11 effector FIP3 controls Rac1 intracellular localization and Rac1 targeting to the immunological synapse. FIP3 regulates, in a Rac1-dependent manner, key morphological events, like T-cell spreading and synapse symmetry. Finally, Rab11-/FIP3-mediated regulation is necessary for T-cell activation leading to cytokine production. Therefore, Rac1 endosomal traffic is key to regulate T-cell activation.

Indexed as

ActinsCD4-Positive T-LymphocytesCell LineCells, CulturedEndosomesHumansI-kappa B KinaseImmunological SynapsesInterleukin-2Jurkat Cellsrab11 GTP-Binding Proteinsrab GTP-Binding Proteinsrac1 GTP-Binding ProteinRNA, Small InterferingActinsI-kappa B KinaseIKBKG protein, humanIL2 protein, humanInterleukin-2rab11 GTP-Binding Proteinsrab GTP-Binding Proteinsrac1 GTP-Binding ProteinRAC1 protein, humanRNA, Small Interferingactin cytoskeletonimmunological synapseintracellular trafficRab11‐FIP3Rac1recycling endosomes

Identifiers

PMID27154205
PMCPMC4863925
OpenAlexW2346515103

What OpenQuestion 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 OpenQuestion graph.