Identification of Unique microRNA Profiles in Different Types of Idiopathic Inflammatory Myopathy

Author:

Muñoz-Braceras Sandra1,Pinal-Fernandez Iago12,Casal-Dominguez Maria12,Pak Katherine1,Milisenda José César134,Lu Shajia5,Gadina Massimo5ORCID,Naz Faiza6,Gutierrez-Cruz Gustavo6,Dell’Orso Stefania6,Torres-Ruiz Jiram17,Grau-Junyent Josep Maria34,Selva-O’Callaghan Albert8ORCID,Paik Julie J.9,Albayda Jemima9,Christopher-Stine Lisa29,Lloyd Thomas E.2ORCID,Corse Andrea M.2,Mammen Andrew L.129

Affiliation:

1. Muscle Disease Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA

2. Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

3. Muscle Research Unit, Internal Medicine Service, Hospital Clinic de Barcelona, 08036 Barcelona, Spain

4. CIBERER, IDIBAPS, University of Barcelona, 08036 Barcelona, Spain

5. Translational Immunology Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA

6. Genomic Technology Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA

7. Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City 14080, Mexico

8. Systemic Autoimmune Diseases Unit, Vall d’Hebron General Hospital, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain

9. Division of Rheumatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA

Abstract

Dermatomyositis (DM), antisynthetase syndrome (AS), immune-mediated necrotizing myopathy (IMNM), and inclusion body myositis (IBM) are four major types of idiopathic inflammatory myopathy (IIM). Muscle biopsies from each type of IIM have unique transcriptomic profiles. MicroRNAs (miRNAs) target messenger RNAs (mRNAs), thereby regulating their expression and modulating transcriptomic profiles. In this study, 18 DM, 12 IMNM, 6 AS, 6 IBM, and 6 histologically normal muscle biopsies underwent miRNA profiling using the NanoString nCounter system. Eleven miRNAs were exclusively differentially expressed in DM compared to controls, seven miRNAs were only differentially expressed in AS, and nine miRNAs were specifically upregulated in IBM. No differentially expressed miRNAs were identified in IMNM. We also analyzed miRNA-mRNA associations to identify putative targets of differentially expressed miRNAs. In DM and AS, these were predominantly related to inflammation and cell cycle progression. Moreover, our analysis showed an association between miR-30a-3p, miR-30e-3p, and miR-199b-5p downregulation in DM and the upregulation of target genes induced by type I interferon. In conclusion, we show that muscle biopsies from DM, AS, and IBM patients have unique miRNA signatures and that these miRNAs might play a role in regulating the expression of genes known to be involved in IIM pathogenesis.

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

MDPI AG

Subject

General Medicine

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