Sex Differences in Expression of Pro-Inflammatory Markers and miRNAs in a Mouse Model of CVB3 Myocarditis

Int J Mol Sci. 2024 Sep 6;25(17):9666. doi: 10.3390/ijms25179666.

Abstract

Myocarditis is an inflammatory disease that may lead to dilated cardiomyopathy. Viral infection of the myocardium triggers immune responses, which involve, among others, macrophage infiltration, oxidative stress, expression of pro-inflammatory cytokines, and microRNAs (miRNAs). The cardioprotective role of estrogen in myocarditis is well documented; however, sex differences in the miRNA expression in chronic myocarditis are still poorly understood, and studying them further was the aim of the present study. Male and female ABY/SnJ mice were infected with CVB3. Twenty-eight days later, cardiac tissue from both infected and control mice was used for real-time PCR and Western blot analysis. NFκB, IL-6, iNOS, TNF-α, IL-1β, MCP-1, c-fos, and osteopontin (OPN) were used to examine the inflammatory state in the heart. Furthermore, the expression of several inflammation- and remodeling-related miRNAs was analyzed. NFκB, IL-6, TNF-α, IL-1β, iNOS, and MCP-1 were significantly upregulated in male mice with CVB3-induced chronic myocarditis, whereas OPN mRNA expression was increased only in females. Further analysis revealed downregulation of some anti-inflammatory miRNA in male hearts (let7a), with upregulation in female hearts (let7b). In addition, dysregulation of remodeling-related miRNAs (miR27b and mir199a) in a sex-dependent manner was observed. Taken together, the results of the present study suggest a sex-specific expression of pro-inflammatory markers as well as inflammation- and remodeling-related miRNAs, with a higher pro-inflammatory response in male CVB3 myocarditis mice.

Keywords: CVB3-induced chronic myocarditis; cardiac inflammation; estrogen; microRNAs; sex differences.

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Coxsackievirus Infections* / genetics
  • Coxsackievirus Infections* / metabolism
  • Coxsackievirus Infections* / virology
  • Cytokines / genetics
  • Cytokines / metabolism
  • Disease Models, Animal*
  • Enterovirus B, Human
  • Female
  • Gene Expression Regulation
  • Inflammation / genetics
  • Inflammation / metabolism
  • Male
  • Mice
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Myocarditis* / genetics
  • Myocarditis* / metabolism
  • Myocarditis* / virology
  • Myocardium / metabolism
  • Myocardium / pathology
  • Sex Characteristics
  • Sex Factors

Substances

  • MicroRNAs
  • Biomarkers
  • Cytokines

Grants and funding

Parts of this work were funded by the DZHK (German Centre for Cardiovascular Research) and by the BMBF (German Ministry of Education and Research). We acknowledge support from the Open Access Publication Fund of the Universitätsklinikum Tübingen.