Non-coding RNA regulation of T cell biology: Implications for age-associated cardiovascular diseases

Exp Gerontol. 2018 Aug:109:38-46. doi: 10.1016/j.exger.2017.06.014. Epub 2017 Jun 23.

Abstract

Prevalence of age-associated cardiovascular diseases (CVD) has dramatically increased as a result of improvements in life expectancy. Chronic inflammation is a shared pathophysiological feature of age-associated CVDs, indicating a role for the immune system in the onset and development of CVDs. Indeed, ageing elicits profound changes in both the cardiovascular and immune system, especially in the T cell compartment. Although such changes have been well described at the cellular level, the molecular mechanisms underlying immune-mediated cardiovascular ageing remain largely unexplored. Non-coding RNAs (ncRNAs) comprise a heterogeneous family of RNA transcripts that regulate gene expression at the epigenetic, transcriptional, post-transcriptional, and post-translational levels. Non-coding RNAs have recently emerged as master modulators of T cell immunity. In this review, the state-of-the-art knowledge on ncRNA regulatory effects over T cell differentiation, function, and ageing in the context of age-associated CVDs, such as atherosclerosis, acute coronary syndromes, and heart failure, is discussed.

Keywords: Cardiovascular ageing; Non-coding RNAs; T cell.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aging / immunology
  • Aging / physiology
  • Cardiovascular Diseases / etiology*
  • Cell Differentiation
  • Humans
  • Inflammation / complications
  • RNA, Untranslated / physiology*
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology*

Substances

  • RNA, Untranslated