Evidence map›Paper›PMID 28368000›Full record

ArticleNature communications2017

Src family kinases Fyn and Lyn are constitutively activated and mediate plasmacytoid dendritic cell responses.

S Dallari, M Macal, M E Loureiro, Y Jo, L Swanson, C Hesser, P Ghosh, E I Zuniga

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. IL-17D reprograms CD93Cellular & molecular immunology · 2026
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  10. Development and function of chicken XCR1Frontiers in immunology · 2023
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Nuclear Functions of the Tyrosine Kinase Src.International journal of molecular sciences · 2020
    Review
  20. Article
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

8 authors at 1 institution in 1 country.

S DallariMolecular Biology Section, Division of Biological Sciences, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
M MacalMolecular Biology Section, Division of Biological Sciences, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
M E LoureiroMolecular Biology Section, Division of Biological Sciences, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
Y JoMolecular Biology Section, Division of Biological Sciences, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
L SwansonDepartments of Medicine and Cellular and Molecular Medicine, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
C HesserMolecular Biology Section, Division of Biological Sciences, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
P GhoshDepartments of Medicine and Cellular and Molecular Medicine, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
E I ZunigaMolecular Biology Section, Division of Biological Sciences, University of California, 9500 Gilman Dr La Jolla, San Diego, California 92093, USA.
University of California, San Diego · US

Funding

Training Grant in GastroenterologyT32DK007202 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PRADIPTA · 1985 to 2022
$7.7M
NIDDK NIH HHS T32 DK007202
6 · The paper itself

Abstract

Plasmacytoid dendritic cells (pDC) are type I interferon-producing cells with critical functions in a number of human illnesses; however, their molecular regulation is incompletely understood. Here we show the role of Src family kinases (SFK) in mouse and human pDCs. pDCs express Fyn and Lyn and their activating residues are phosphorylated both before and after Toll-like receptor (TLR) stimulation. Fyn or Lyn genetic ablation as well as treatment with SFK inhibitors ablate pDC (but not conventional DC) responses both in vitro and in vivo. Inhibition of SFK activity not only alters TLR-ligand localization and inhibits downstream signalling events, but, independent of ex-vivo TLR stimulation, also affects constitutive phosphorylation of BCAP, an adaptor protein bridging PI3K and TLR pathways. Our data identify Fyn and Lyn as important factors that promote pDC responses, describe the mechanisms involved and highlight a tonic SFK-mediated signalling that precedes pathogen encounter, raising the possibility that small molecules targeting SFKs could modulate pDC responses in human diseases.

Indexed as

AnimalsCarrier ProteinsCytokinesCytomegalovirus InfectionsDendritic CellsEndosomesEnzyme ActivationHumansLigandsMice, Inbred C57BLMuromegalovirusPhosphorylationProtein TransportProto-Oncogene Proteins c-fynPyrimidinesSignal TransductionbafetinibCarrier ProteinsCytokinesLigandslyn protein-tyrosine kinaseODF2L protein, humanProto-Oncogene Proteins c-fynPyrimidinessrc-Family KinasesToll-Like ReceptorsTOR Serine-Threonine Kinases

Identifiers

PMID28368000
PMCPMC5382270
OpenAlexW2604905413

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.