Abstract | BACKGROUND AND AIMS:
Myocarditis is inflammation in the heart; its pathogenesis is to be further investigated. Activities of micro RNAs (miR) are associated with immune inflammation. This study tests a hypothesis that miR-98 is involved in the development of myocarditis. METHODS: RESULTS: Mice immunized with MyHC-α showed myocarditis and lower frequency of IL-10+ B cells (B10 cell) in the hearts. Expression of miR-98 was higher, IL-10 was lower, in B cells isolated from the mouse hearts with myocarditis, which was negatively correlated with each other. Exposure to tumor necrosis factor-α up regulated miR-98 expression in B cells. Over-expression of miR-98 suppressed IL-10 expression in B cells. Blocking miR-98 or adoptively transplanting B10 cells attenuated experimental myocarditis. CONCLUSIONS: miR-98 suppresses IL-10 expression in B cells in the heart, which plays an important role in myocarditis. MiR-98 may be a therapeutic target in the treatment of myocarditis.
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Authors | Xiao Chen, Shuo Dong, Ningning Zhang, Liang Chen, Mao-Gang Li, Ping-Chang Yang, Jiangping Song |
Journal | International journal of cardiology
(Int J Cardiol)
Vol. 229
Pg. 75-81
(Feb 15 2017)
ISSN: 1874-1754 [Electronic] Netherlands |
PMID | 27913008
(Publication Type: Journal Article)
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Copyright | Copyright © 2016 Elsevier Ireland Ltd. All rights reserved. |
Chemical References |
- MIRN98 microRNA, human
- MicroRNAs
- Interleukin-10
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Topics |
- Adult
- Animals
- B-Lymphocytes
(immunology, metabolism)
- Cells, Cultured
- Disease Models, Animal
- Enzyme-Linked Immunosorbent Assay
- Female
- Flow Cytometry
- Gene Expression Regulation
- Humans
- Immunity, Cellular
- Interleukin-10
(biosynthesis, genetics)
- Male
- Mice
- Mice, Inbred BALB C
- MicroRNAs
(biosynthesis, genetics)
- Middle Aged
- Myocarditis
(genetics, immunology, metabolism)
- Myocardium
(metabolism, pathology)
- Real-Time Polymerase Chain Reaction
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