Evidence map›Paper›PMID 26034069›Full record

ArticleJournal of cell science2015

The small GTPase Rab8 interacts with VAMP-3 to regulate the delivery of recycling T-cell receptors to the immune synapse.

Francesca Finetti, Laura Patrussi, Donatella Galgano, Chiara Cassioli, Giuseppe Perinetti, Gregory J Pazour, Cosima T Baldari

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 65 citations in OpenAlex.

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  7. Membrane Fusion and SNAREs: Interaction with Ras Proteins.International journal of molecular sciences · 2022
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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

7 authors at 3 institutions in 2 countries.

Francesca FinettiDepartment of Life Sciences, University of Siena, Siena 53100, Italy.
Laura PatrussiDepartment of Life Sciences, University of Siena, Siena 53100, Italy.
Donatella GalganoDepartment of Life Sciences, University of Siena, Siena 53100, Italy.
Chiara CassioliDepartment of Life Sciences, University of Siena, Siena 53100, Italy.
Giuseppe PerinettiDepartment of Medical, Surgical and Health Sciences, School of Dentistry, University of Trieste, Trieste 34129, Italy.
Gregory J PazourProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Cosima T BaldariDepartment of Life Sciences, University of Siena, Siena 53100, Italy cosima.baldari@unisi.it.
University of Siena · ITUniversity of Massachusetts Chan Medical School · USUniversity of Trieste · IT

Funding

Intraflagellar Transport Proteins in MiceR01GM060992 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Gregory J Pazour · 2001 to 2026
$10.3M
NIGMS NIH HHS R01 GM060992Telethon GGP11021
6 · The paper itself

Abstract

IFT20, a component of the intraflagellar transport (IFT) system that controls ciliogenesis, regulates immune synapse assembly in the non-ciliated T-cell by promoting T-cell receptor (TCR) recycling. Here, we have addressed the role of Rab8 (for which there are two isoforms Rab8a and Rab8b), a small GTPase implicated in ciliogenesis, in TCR traffic to the immune synapse. We show that Rab8, which colocalizes with IFT20 in Rab11(+) endosomes, is required for TCR recycling. Interestingly, as opposed to in IFT20-deficient T-cells, TCR(+) endosomes polarized normally beneath the immune synapse membrane in the presence of dominant-negative Rab8, but were unable to undergo the final docking or fusion step. This could be accounted for by the inability of the vesicular (v)-SNARE VAMP-3 to cluster at the immune synapse in the absence of functional Rab8, which is responsible for its recruitment. Of note, and similar to in T-cells, VAMP-3 interacts with Rab8 at the base of the cilium in NIH-3T3 cells, where it regulates ciliary growth and targeting of the protein smoothened. The results identify Rab8 as a new player in vesicular traffic to the immune synapse and provide insight into the pathways co-opted by different cell types for immune synapse assembly and ciliogenesis.

Indexed as

AnimalsEndosomesHumansImmunological SynapsesJurkat CellsMiceNIH 3T3 Cellsrab GTP-Binding ProteinsReceptors, Antigen, T-CellSNARE ProteinsVesicle-Associated Membrane Protein 3RAB8A protein, humanRab8 protein, mouserab GTP-Binding ProteinsReceptors, Antigen, T-CellSNARE ProteinsVAMP3 protein, humanVesicle-Associated Membrane Protein 3vesicle-associated membrane protein 3, mouseImmune synapseRab8TCR recycling

Identifiers

PMID26034069
PMCPMC4510855
OpenAlexW2161482087

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.