Evidence map›Paper›PMID 33291448›Full record

ArticleInternational journal of molecular sciences2020

miR-155 Contributes to Normal Keratinocyte Differentiation and Is Upregulated in the Epidermis of Psoriatic Skin Lesions.

Lucian Beer, Polina Kalinina, Martin Köcher, Maria Laggner, Markus Jeitler, Salman Abbas Zadeh, Dragan Copic, Erwin Tschachler, Michael Mildner

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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  14. Skin Epidermis and Barrier Function.International journal of molecular sciences · 2021
    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

9 authors at 2 institutions in 1 country.

Lucian BeerDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0003-4388-7580
Polina KalininaDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.
Martin KöcherDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.
Maria LaggnerDivision of Thoracic Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Markus JeitlerCore Facility Genomics, Medical University of Vienna, 1090 Vienna, Austria.
Salman Abbas ZadehDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-5994-3682
Dragan CopicDivision of Thoracic Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Erwin TschachlerDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.
Michael MildnerDepartment of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-6892-925X
Medical University of Vienna · ATAustrian Cluster for Tissue Regeneration · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of microRNAs (miRNAs) during keratinocyte (KC) differentiation and in skin diseases with epidermal phenotypes has attracted strong interest over the past few years. However, combined mRNA and miRNA expression analyses to elucidate the intricate mRNA-miRNA networks of KCs at different stages of differentiation have not been performed yet. In the present study, we investigated the dynamics of miRNA and mRNA expression during KC differentiation in vitro and in normal and psoriatic epidermis. While we identified comparable numbers of up- and downregulated mRNAs (49% and 51%, respectively), miRNAs were predominantly upregulated (76% vs 24%) during KC differentiation. Further bioinformatics analyses suggested an important inhibitory role for miR-155 in KC differentiation, as it was repressed during KC differentiation in normal skin but strongly upregulated in the epidermis of psoriatic skin lesions. Mimicking the inflammatory milieu of psoriatic skin in vitro, we could show that the pro-inflammatory cytokines IL17, IL1β and INFγ synergistically upregulated miR-155 expression in KCs. Forced over-expression of miR-155 in human in vitro skin models specifically reduced the expression of loricrin (LOR) in KCs, indicating that miR-155 interferes with the establishment of a normal epidermal barrier. Together, our data indicate that downregulation of miR-155 during KC differentiation is a crucial step for epidermal barrier formation. Furthermore, its strong upregulation in psoriatic lesions suggests a contributing role of miR-155 in the altered keratinocyte differentiation observed in psoriasis. Therefore, miR-155 represents as a potential target for treating psoriatic skin lesions.

Indexed as

Gene Expression RegulationCell DifferentiationComputational BiologyCytokinesDisease SusceptibilityEpidermal CellsEpidermisGene Expression ProfilingGene Regulatory NetworksHumansInflammation MediatorsKeratinocytesMicroRNAsPsoriasisRNA InterferenceRNA, MessengerCytokinesInflammation MediatorsMicroRNAsMIRN155 microRNA, humanRNA, Messengerepidermal keratinocytesepidermiskeratinocyte differentiationmiRNAmRNApsoriasisskin

Identifiers

PMID33291448
PMCPMC7731132
OpenAlexW3112521142

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.