Evidence map›Paper›PMID 34557075›Full record

ArticleFrontiers in cellular neuroscience2021

Expression of IL-20 Receptor Subunit β Is Linked to EAE Neuropathology and CNS Neuroinflammation.

Jacquelyn R Dayton, Yinyu Yuan, Lisa P Pacumio, Bryce G Dorflinger, Samantha C Yoo, Mariah J Olson, Sara I Hernández-Suárez, Moira M McMahon, Lillian Cruz-Orengo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Jacquelyn R DaytonDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Yinyu YuanDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Lisa P PacumioDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Bryce G DorflingerDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Samantha C YooDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Mariah J OlsonDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Sara I Hernández-SuárezDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Moira M McMahonDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
Lillian Cruz-OrengoDepartment of Anatomy, Physiology and Cell Biology, University of California, Davis, Davis, CA, United States.
University of California, Davis · USUniversity of California, Berkeley · US

Funding

UC Davis Environmental Health Sciences Core CenterP30ES023513 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Irva Hertz-Picciotto · 2015 to 2026
$26.0M
Elucidating the Role of IL-20 Signaling Through IL-20RB in the Neuropathogenesis of Multiple SclerosisR21NS111431 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CRUZ-ORENGO, LILLIAN · 2019 to 2019
$413k
NIEHS NIH HHS P30 ES023513NINDS NIH HHS R21 NS111431
6 · The paper itself

Abstract

Considerable clinical evidence supports that increased blood-brain barrier (BBB) permeability is linked to immune extravasation of CNS parenchyma during neuroinflammation. Although BBB permeability and immune extravasation are known to be provoked by vascular endothelial growth factor-A (i.e., VEGF-A) and C-X-C motif chemokine ligand 12 (CXCL12), respectively, the mechanisms that link both processes are still elusive. The interleukin-20 (i.e., IL-20) cytokine signaling pathway was previously implicated in VEGF-mediated angiogenesis and is known to induce cellular response by way of signaling through IL-20 receptor subunit β (i.e., IL-20RB). Dysregulated IL-20 signaling is implicated in many inflammatory pathologies, but it's contribution to neuroinflammation has yet to be reported. We hypothesize that the IL-20 cytokine, and the IL cytokine subfamily more broadly, play a key role in CNS neuroinflammation by signaling through IL-20RB, induce VEGF activity, and enhance both BBB-permeability and CXCL12-mediated immune extravasation. To address this hypothesis, we actively immunized

Indexed as

experimental autoimmune encephalomyelitisHCMEC/D3 cellsIL-20 subfamilymicrovesselMOG-Th1 cells

Identifiers

PMID34557075
PMCPMC8452993
OpenAlexW3197810423

What Socratic 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 Socratic graph.