Evidence map›Paper›PMID 26972013›Full record

ArticleCell reports2016

The SNARE VAMP7 Regulates Exocytic Trafficking of Interleukin-12 in Dendritic Cells.

Giulia Chiaruttini, Giulia M Piperno, Mabel Jouve, Francesca De Nardi, Paola Larghi, Andrew A Peden, Gabriele Baj, Sabina Müller, Salvatore Valitutti, Thierry Galli and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 47 citations in OpenAlex.

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  13. ATP redirects cytokine trafficking and promotes novel membrane TNF signalingFASEB journal : official publication of the Federation of American Societies for Experimental 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

11 authors at 6 institutions in 3 countries.

Giulia ChiaruttiniInternational Centre for Genetic Engineering and Biotechnology, Padriciano 99, 34149 Trieste, Italy.
Giulia M PipernoInternational Centre for Genetic Engineering and Biotechnology, Padriciano 99, 34149 Trieste, Italy.
Mabel JouveGénétique et Biologie du Développement, UMR 3215, 26 rue d'Ulm, 75005 Paris, France.
Francesca De NardiInternational Centre for Genetic Engineering and Biotechnology, Padriciano 99, 34149 Trieste, Italy.
Paola LarghiDepartment of Pathophysiology and Transplantation, University of Milan, via F. Sforza 35, 20122 Milan, Italy; Istituto Nazionale Genetica Molecolare "Romeo ed Enrica Invernizzi," via F. Sforza 35, 20122 Milan, Italy.
Andrew A PedenCentre for Membrane Interactions and Dynamics, Department of Biomedical Science, The University of Sheffield, Western Bank, Sheffield S10 2TN, UK.
Gabriele BajLife Sciences Department, University of Trieste, via Giorgieri 5, 34127 Trieste, Italy.
Sabina MüllerCentre de Physiopathologie Toulouse-Purpan, Toulouse, INSERM UMR 1043, Toulouse 31300, France.
Salvatore ValituttiCentre de Physiopathologie Toulouse-Purpan, Toulouse, INSERM UMR 1043, Toulouse 31300, France.
Thierry GalliInstitut Jacques Monod, UMR 7592, Centre National de la Recherche Scientifique, Université Paris Diderot, Sorbonne Paris Cité, 75013 Paris, France; Membrane Traffic in Neuronal and Epithelial Morphogenesis, INSERM ERL U950, 75013 Paris, France.
Federica BenvenutiInternational Centre for Genetic Engineering and Biotechnology, Padriciano 99, 34149 Trieste, Italy. Electronic address: benvenuti@icgeb.org.
International Centre for Genetic Engineering and Biotechnology · ITInserm · FRIstituto Nazionale Genetica Molecolare · ITLaboratoire de Biologie du Développement · FRUniversity of Sheffield · GBUniversity of Trieste · IT

Funding

Biotechnology and Biological Sciences Research Council BB/L022389/1Medical Research Council G120/952
6 · The paper itself

Abstract

Interleukin-12 (IL-12), produced by dendritic cells in response to activation, is central to pathogen eradication and tumor rejection. The trafficking pathways controlling spatial distribution and intracellular transport of IL-12 vesicles to the cell surface are still unknown. Here, we show that intracellular IL-12 localizes in late endocytic vesicles marked by the SNARE VAMP7. Dendritic cells (DCs) from VAMP7-deficient mice are partially impaired in the multidirectional release of IL-12. Upon encounter with antigen-specific T cells, IL-12-containing vesicles rapidly redistribute at the immune synapse and release IL-12 in a process entirely dependent on VAMP7 expression. Consistently, acquisition of effector functions is reduced in T cells stimulated by VAMP7-null DCs. These results provide insights into IL-12 intracellular trafficking pathways and show that VAMP7-mediated release of IL-12 at the immune synapse is a mechanism to transmit innate signals to T cells.

Indexed as

AnimalsBone Marrow CellsCell DifferentiationCells, CulturedDendritic CellsExocytosisInterleukin-12MaleMiceMice, Inbred C57BLMice, KnockoutMicroscopy, ConfocalMicroscopy, VideoPhosphotransferasesrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsCdk5r1 protein, mouseInterleukin-12Phosphotransferasesrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsRNA, Small InterferingR-SNARE ProteinsSybl1 protein, mouse

Identifiers

PMID26972013
PMCPMC4806224
OpenAlexW2296173401

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.