4.3 Article

MyomiRs in cultured muscle cells from patients with idiopathic inflammatory myopathy are modulated by disease but not by 6-month exercise training

期刊

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
卷 40, 期 2, 页码 346-357

出版社

CLINICAL & EXPER RHEUMATOLOGY

关键词

myositis; exercise; muscle cells; microRNAs; lipid metabolism

资金

  1. [MZCR NU21-05-00322]
  2. [VEGA 2/0091/19]
  3. [MZCR 16-33574A]
  4. [SAS-MOST JRP 10/2018]
  5. [APVV 20/0466]
  6. [VEGA 0107/18]

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This study found that microRNAs involved in myogenesis and regeneration in muscle cells were upregulated in patients with idiopathic inflammatory myopathies (IIM). Furthermore, these microRNAs were associated with the metabolic profile of muscle cells and clinical parameters, suggesting their role in modulating muscle metabolism and the clinical state of patients.
Objective Idiopathic inflammatory myopathies/IIM are associated with changes in muscle-specific microRNA/miR. Exercise improves muscle function and metabolism in parallel with changes in miR expression. We investigated the effects of disease and exercise on miRs in differentiated muscle cells/myotubes from IIM patients and controls. Methods Samples of m. vastus lateralis were obtained by needle biopsy from IIM patients before/after 6-month training and from matched sedentary healthy controls. Muscle cell cultures were established and exposed to saturated fatty acid during differentiation. MiR-133a,-133b,-206,-1 and their target genes (qPCR), fat oxidation (FOx), lipids (chromatography) and mitochondrial oxidative phosphorylation (OxPHOS) complexes (immunoblotting) were measured. Interrelations between in vitro miRs and metabolism of myotubes as well as clinical parameters and disease activity/MITAX were explored. Results Levels of miRs were higher in myotubes derived from IIM patients compared to healthy controls (up to 3.5-fold, p<0.05). Neither 6-month training (IIM patients) nor in vitro palmitate treatment modulated myomiRs in myotubes. However, miR-133a,-133b, and miR-1 correlated negatively with FOx (p<0.01), triacylglycerols (p<0.05) and OxPHOS complex-V (p<0.05) and positively with OxPHOS complex-I (p<0.05) in myotubes. MiR-133a and miR-133b in myotubes were related to disease activity and fasting glycaemia in vivo (both p<0.05). Conclusion Upregulation of microRNAs involved in myogenesis and regeneration in muscle cells derived from IIM patients indicates activation of compensatory epigenetic mechanisms, potentially aimed to counteract disease progression. Relationships of microRNAs with in vitro metabolic profile of muscle cells as well as with clinical parameters support the role of muscle-specific microRNAs in modulating muscle metabolism and clinical state of patients.

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