MicroRNA-17-5p Reduces Inflammation and Bone Erosions in Mice With Collagen-Induced Arthritis and Directly Targets the JAK/STAT Pathway in Rheumatoid Arthritis Fibroblast-like Synoviocytes.


Journal

Arthritis & rheumatology (Hoboken, N.J.)
ISSN: 2326-5205
Titre abrégé: Arthritis Rheumatol
Pays: United States
ID NLM: 101623795

Informations de publication

Date de publication:
12 2020
Historique:
received: 05 12 2019
accepted: 02 07 2020
pubmed: 20 7 2020
medline: 5 1 2021
entrez: 20 7 2020
Statut: ppublish

Résumé

We undertook this study to examine microRNA (miRNA) expression across rheumatoid arthritis (RA) phenotypes, along with the effects and mechanisms of action of miRNA-17-5p (miR-17). A miRNA array was performed in synovial tissue biopsied from patients with naive erosive RA (n = 3) and patients with nonerosive RA (n = 3). MicroRNA-17 lipoplex was delivered intraarticularly in the murine collagen-induced arthritis model. Clinical, histologic, and structural effects were studied over the course of arthritis. In-depth studies of the mechanisms of action of miR-17 were performed in primary RA fibroblast-like synoviocytes (FLS) isolated from synovial tissue. Fifty-five miRNAs including miR-17 were reduced in erosive RA. The miR-17 transfection into arthritic paws reduced the clinical inflammation score between day 2 and day 7 (2.8 versus 1.9; P = 0.03). Synovial B cell, T cell, macrophage, and polynuclear neutrophil infiltration was significantly reduced. Structural damage was also decreased, as shown by a reduction in the number of osteoclasts detected using tartrate-resistant acid phosphatase staining (osteoclast surface/bone surface 32% versus 18%; P = 0.005) and erosion score by computed tomography analysis (2.9 versus 1.7; P = 0.023). Proinflammatory cytokines from the interleukin-6 (IL-6) family and IL-1β expression were also significantly reduced, but tumor necrosis factor was not. MicroRNA-17 directly targeted the 3'-untranslated regions of STAT3 and JAK1. STAT3 and JAK1 messenger RNA (mRNA) and protein expression were reduced in RA FLS following miR-17 transfection. STAT3 and JAK1 mRNA and activation of STAT3, as assessed by immunohistochemistry, were also reduced in injected paws (% stained area 93% versus 62%; P = 0.035). We demonstrate an antiinflammatory and antierosive role of miR-17 in vivo. This effect involves the suppression of the IL-6 family autocrine-amplifying loop through the direct targeting of JAK1 and STAT3.

Identifiants

pubmed: 32683798
doi: 10.1002/art.41441
doi:

Substances chimiques

Cytokines 0
MIRN17 microRNA, human 0
MicroRNAs 0
STAT Transcription Factors 0
Janus Kinases EC 2.7.10.2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2030-2039

Informations de copyright

© 2020 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.

Références

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Auteurs

Aurélie Najm (A)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, Nantes, France, and University of Glasgow College of Medical Veterinary and Life Sciences, Glasgow, UK.

François-Marie Masson (FM)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, Nantes, France.

Pauline Preuss (P)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, and Nantes University Hospital, Nantes, France.

Steven Georges (S)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, Nantes, France.

Benjamin Ory (B)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, Nantes, France.

Thibaut Quillard (T)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, Nantes, France.

Shatakshi Sood (S)

University of Glasgow College of Medical Veterinary and Life Sciences, Glasgow, UK.

Carl S Goodyear (CS)

University of Glasgow College of Medical Veterinary and Life Sciences, Glasgow, UK.

Douglas J Veale (DJ)

St. Vincent's University Hospital and University College Dublin School of Medicine, Dublin, Ireland.

Ursula Fearon (U)

Trinity College Dublin, Dublin, Ireland.

Benoit Le Goff (B)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, and Nantes University Hospital, Nantes, France.

Frédéric Blanchard (F)

PHY-OS Laboratory, INSERM UMR 1238, Nantes University of Medicine, Nantes, France.

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