TY - JOUR
T1 - Identification of Unique microRNA Profiles in Different Types of Idiopathic Inflammatory Myopathy
AU - Muñoz-Braceras, Sandra
AU - Pinal-Fernandez, Iago
AU - Casal-Dominguez, Maria
AU - Pak, Katherine
AU - Milisenda, José César
AU - Lu, Shajia
AU - Gadina, Massimo
AU - Naz, Faiza
AU - Gutierrez-Cruz, Gustavo
AU - Dell'Orso, Stefania
AU - Torres-Ruiz, Jiram
AU - Grau-Junyent, Josep Maria
AU - Selva O'Callaghan, Albert
AU - Paik, Julie J.
AU - Albayda, Jemima
AU - Christopher-Stine, Lisa
AU - Lloyd, Thomas E.
AU - Corse, Andrea
AU - Mammen, Andrew L.
PY - 2023
Y1 - 2023
N2 - 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.
AB - 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.
KW - Inflammatory myopathies
KW - Myositis
KW - Mirna
KW - NanoString
KW - Ncounter
UR - https://www.scopus.com/pages/publications/85170161517
U2 - 10.3390/cells12172198
DO - 10.3390/cells12172198
M3 - Article
C2 - 37681930
SN - 2073-4409
VL - 12
JO - Cells
JF - Cells
ER -