Evidence map›Paper›PMID 28266599›Full record

ArticleScientific reports2017

Double-stranded RNA induces inflammation via the NF-κB pathway and inflammasome activation in the outer root sheath cells of hair follicles.

Jung-Min Shin, Dae-Kyoung Choi, Kyung-Cheol Sohn, Soo-Yeon Kim, Jeong Min Ha, Young Ho Lee, Myung Im, Young-Joon Seo, Chang Deok Kim, Jeung-Hoon Lee and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 34 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

11 authors at 1 institution in 1 country.

Jung-Min ShinDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Dae-Kyoung ChoiDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Kyung-Cheol SohnDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Soo-Yeon KimDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Jeong Min HaDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Young Ho LeeDepartment of Anatomy, School of Medicine, Chungnam National University, Daejeon, Korea.
Myung ImDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Young-Joon SeoDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Chang Deok KimDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Jeung-Hoon LeeDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Young LeeDepartment of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea.
Chungnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alopecia areata (AA), a chronic, relapsing, hair-loss disorder, is considered to be a T cell-mediated autoimmune disease. It affects approximately 1.7% of the population, but its precise pathogenesis remains to be elucidated. Despite the recent attention focused on the roles of inflammasomes in the pathogenesis of autoinflammatory diseases, little is known about inflammasome activation in AA. Thus, in this study, we investigated the pattern of NLRP3 inflammasome activation in the outer root sheath (ORS) cells of hair follicles. We found that interleukin (IL)-1β and caspase-1 expression was increased in hair follicle remnants and inflammatory cells of AA tissue specimens. After stimulation of ORS cells with the double-stranded (ds)RNA mimic polyinosinic:polycytidylic acid (poly[I:C]), the activation of caspase-1 and secretion of IL-1β were enhanced. Moreover, NLRP3 knockdown decreased this poly(I:C)-induced IL-1β production. Finally, we found that high-mobility group box 1 (HMGB1) translocated from the nucleus to the cytosol and was secreted into the extracellular space by inflammasome activation. Taken together, these findings suggest that ORS cells are important immunocompetent cells that induce NLRP3 inflammasomes. In addition, dsRNA-induced IL-1β and HMGB1 secretion from ORS cells may contribute to clarifying the pathogenesis and therapeutic targets of AA.

Indexed as

Cell Line, TransformedHair FollicleHMGB1 ProteinHumansInflammasomesInflammationInterleukin-1betaNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPoly I-CRNA, Double-StrandedSignal TransductionHMGB1 ProteinHMGB1 protein, humanIL1B protein, humanInflammasomesInterleukin-1betaNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanPoly I-CRNA, Double-Stranded

Identifiers

PMID28266599
PMCPMC5339809
OpenAlexW2592499913

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Registered trials

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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.