Evidence map›Paper›PMID 29326695›Full record

ArticleFrontiers in immunology2017

Caveolin-1 Expression Increases upon Maturation in Dendritic Cells and Promotes Their Migration to Lymph Nodes Thereby Favoring the Induction of CD8

Cesar Oyarce, Sebastián Cruz-Gomez, Felipe Galvez-Cancino, Pablo Vargas, Hélène D Moreau, Natalia Diaz-Valdivia, Jorge Diaz, Flavio Andres Salazar-Onfray, Rodrigo Pacheco, Ana Maria Lennon-Dumenil and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  8. Observational
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  11. Membrane Compartmentalization and Scaffold Proteins in Leukocyte Migration.Frontiers in cell and developmental biology · 2020
    Review
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  17. Adhesive Interactions Delineate the Topography of the Immune Synapse.Frontiers in cell and developmental biology · 2018
    Review
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

12 authors at 5 institutions in 2 countries.

Cesar OyarceLaboratory of Gene Immunotherapy, Fundación Ciencia & Vida, Santiago, Chile.
Sebastián Cruz-GomezLaboratory of Gene Immunotherapy, Fundación Ciencia & Vida, Santiago, Chile.
Felipe Galvez-CancinoLaboratory of Gene Immunotherapy, Fundación Ciencia & Vida, Santiago, Chile.
Pablo VargasInstitut National de la Santé et de la Recherche Médicale Unité 144, Institut Curie/CNRS, Paris, France.
Hélène D MoreauInstitut National de la Santé et de la Recherche Médicale Unité 932, Institut Curie/CNRS, Paris, France.
Natalia Diaz-ValdiviaLaboratory of Cellular Communication, Advanced Center for Chronic Diseases (ACCDiS) and Center for Molecular Studies of the Cell (CEMC), Program in Cell and Molecular Biology, Faculty of Medicine, Biomedical Sciences Institute (ICBM), University of Chile, Santiago, Chile.
Jorge DiazLaboratory of Cellular Communication, Advanced Center for Chronic Diseases (ACCDiS) and Center for Molecular Studies of the Cell (CEMC), Program in Cell and Molecular Biology, Faculty of Medicine, Biomedical Sciences Institute (ICBM), University of Chile, Santiago, Chile.
Flavio Andres Salazar-OnfrayProgram in Immunology, Faculty of Medicine, Biomedical Sciences Institute (ICBM), University of Chile, Santiago, Chile.
Rodrigo PachecoLaboratory of Neuroimmunology, Fundación Ciencia & Vida, Santiago, Chile.
Ana Maria Lennon-DumenilInstitut National de la Santé et de la Recherche Médicale Unité 932, Institut Curie/CNRS, Paris, France.
Andrew F G QuestLaboratory of Cellular Communication, Advanced Center for Chronic Diseases (ACCDiS) and Center for Molecular Studies of the Cell (CEMC), Program in Cell and Molecular Biology, Faculty of Medicine, Biomedical Sciences Institute (ICBM), University of Chile, Santiago, Chile.
Alvaro LladserLaboratory of Gene Immunotherapy, Fundación Ciencia & Vida, Santiago, Chile.
University of Chile · CLFundación Ciencia and Vida · CLInserm · FRCentre National de la Recherche Scientifique · FRUniversidad Andrés Bello · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cell (DC) trafficking from peripheral tissues to lymph nodes (LNs) is a key step required to initiate T cell responses against pathogens as well as tumors. In this context, cellular membrane protrusions and the actin cytoskeleton are essential to guide DC migration towards chemotactic signals. Caveolin-1 (CAV1) is a scaffolding protein that modulates signaling pathways leading to remodeling of the actin cytoskeleton and enhanced migration of cancer cells. However, whether CAV1 is relevant for DC function and specifically for DC migration to LNs is unknown. Here, we show that CAV1 expression is upregulated in DCs upon LPS- and TNF-α-induced maturation. CAV1 deficiency did not affect differentiation, maturation, or the ability of DCs to activate CD8

Indexed as

antitumor immune responsecaveolin-1CD8+ T cell activationchemotaxisdendritic cellsmigration

Identifiers

PMID29326695
PMCPMC5733362
OpenAlexW2773677967

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.