MicroRNA involvement in immune activation during heart failure

Cardiovasc Drugs Ther. 2011 Apr;25(2):161-70. doi: 10.1007/s10557-011-6291-y.

Abstract

Heart failure is one of the common end stages of cardiovascular diseases, the leading cause of death in developed countries. Molecular mechanisms underlying the development of heart failure remain elusive but there is a consistent observation of chronic immune activation and aberrant microRNA (miRNA) expression that is present in failing hearts. This review will focus on the interplay between the immune system and miRNAs as factors that play a role during the development of heart failure. Several studies have shown that heart failure patients can be characterized by a sustained innate immune activation. The role of inflammatory signaling is discussed and TLR4 signaling, IL-1β, TNFα and IL-6 expression appears to coincide with the development of heart failure. Furthermore, we describe the implication of the renin angiotensin aldosteron system in immunity and heart failure. In the past decade microRNAs (miRNAs), small non-coding RNAs that translationally repress protein synthesis by binding to partially complementary sequences of mRNA, have come to light as important regulators of several kinds of cardiovascular diseases including cardiac hypertrophy and heart failure. The involvement of differentially expressed miRNAs in the inflammation that occurs during the development of heart failure is still subject of investigation. Here, we summarize and comment on the first studies in this field and hypothesize on the putative involvement of certain miRNAs in heart failure. MicroRNAs have been shown to be critical regulators of cardiac function and inflammation. Future research will have to point out if dampening the immune response, and the miRNAs associated with it, during the development of heart failure is a therapeutically plausible route to follow.

Publication types

  • Review

MeSH terms

  • Cardiovascular Diseases / genetics
  • Cardiovascular Diseases / immunology
  • Cytokines / physiology
  • Heart Failure / genetics
  • Heart Failure / immunology*
  • Humans
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • MicroRNAs / immunology
  • MicroRNAs / physiology*
  • Myocardium / immunology*
  • Myocardium / metabolism
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Renin-Angiotensin System / physiology
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Interleukin-6
  • MicroRNAs
  • NF-kappa B
  • Tumor Necrosis Factor-alpha