Evidence map›Paper›PMID 34301846›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2021

Investigation of Fascin1, a Marker of Mature Dendritic Cells, Reveals a New Role for IL-6 Signaling in CCR7-Mediated Chemotaxis.

Fumio Matsumura, Robin Polz, Sukhwinder Singh, Aya Matsumura, Jürgen Scheller, Shigeko Yamashiro

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. EZH2 elicits CD8Communications biology · 2024
    Article
  5. Article
  6. 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

6 authors at 3 institutions in 3 countries.

Fumio MatsumuraDepartment of Molecular Biology and Biochemistry, Rutgers-New Brunswick, Piscataway, NJ; yamashiro@dls.rutgers.edu matsumura@dls.rutgers.edu.
Robin PolzInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich-Heine-University Dusseldorf, Dusseldorf, Germany.
Sukhwinder SinghDepartment of Pathology, Immunology and Laboratory Medicine, Rutgers New Jersey Medical School, Newark, NJ; and.
Aya MatsumuraGraduate School of Science, Nagoya University, Nagoya, Japan.
Jürgen SchellerInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich-Heine-University Dusseldorf, Dusseldorf, Germany.ORCID 0000-0001-9932-1055
Shigeko YamashiroDepartment of Molecular Biology and Biochemistry, Rutgers-New Brunswick, Piscataway, NJ; yamashiro@dls.rutgers.edu matsumura@dls.rutgers.edu.ORCID 0000-0001-7207-9406
Rutgers, The State University of New Jersey · USHeinrich Heine University Düsseldorf · DENagoya University · JP

Funding

Role of fascin1 in dendritic cell-mediated immunity against listeria infectionR03AI099315 · NIAID · RUTGERS, THE STATE UNIV OF N.J. · PI MATSUMURA, FUMIO, YAMASHIRO, SHIGEKO · 2012 to 2013
$155k
NIAID NIH HHS R03 AI099315
6 · The paper itself

Abstract

Migration of mature dendritic cells (DCs) to lymph nodes is critical for the initiation of adaptive immunity. CCR7, a G-protein-coupled receptor for CCL19/21 chemokines, is known to be essential for chemotaxis of mature DCs, but the molecular mechanism linking inflammation to chemotaxis remains unclear. We previously demonstrated that fascin1, an actin-bundling protein, increases chemotaxis of mature mouse DCs. In this article, we demonstrated that fascin1 enhanced IL-6 secretion and signaling of mature mouse DCs. Furthermore, we demonstrated that IL-6 signaling is required for chemotaxis. Blockage of IL-6 signaling in wild-type DCs with an anti-IL-6 receptor α (IL-6Rα) Ab inhibited chemotaxis toward CCL19. Likewise, knockout of IL-6Rα inhibited chemotaxis of bone marrow-derived DCs. The addition of soluble IL-6Rα and IL-6 rescued chemotaxis of IL-6Rα knockout bone marrow-derived DCs, underscoring the role of IL-6 signaling in chemotaxis. We found that IL-6 signaling is required for internalization of CCR7, the initial step of CCR7 recycling. CCR7 recycling is essential for CCR7-mediated chemotaxis, explaining why IL-6 signaling is required for chemotaxis of mature DCs. Our results have identified IL-6 signaling as a new regulatory pathway for CCR7/CCL19-mediated chemotaxis and suggest that rapid migration of mature DCs to lymph nodes depends on inflammation-associated IL-6 signaling.

Indexed as

AnimalsAntibodies, BlockingAntigens, DifferentiationCell DifferentiationCells, CulturedChemotaxisDendritic CellsGene Expression RegulationInterleukin-6MiceMice, KnockoutMicrofilament ProteinsReceptors, CCR7Receptors, Interleukin-6Receptors, OdorantSignal TransductionAntibodies, BlockingAntigens, DifferentiationCcr7 protein, mouseIl6ra protein, mouseInterleukin-6Microfilament ProteinsOlfr73 protein, mouseReceptors, CCR7Receptors, Interleukin-6Receptors, Odorant

Identifiers

PMID34301846
PMCPMC8360331
OpenAlexW3186169628

What OpenQuestion holds

Textmetadata
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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.