LARP7 ameliorates cellular senescence and aging by allosterically enhancing SIRT1 deacetylase activity

Cell Rep. 2021 Nov 23;37(8):110038. doi: 10.1016/j.celrep.2021.110038.

Abstract

Cellular senescence is associated with pleiotropic physiopathological processes, including aging and age-related diseases. The persistent DNA damage is a major stress leading to senescence, but the underlying molecular link remains elusive. Here, we identify La Ribonucleoprotein 7 (LARP7), a 7SK RNA binding protein, as an aging antagonist. DNA damage-mediated Ataxia Telangiectasia Mutated (ATM) activation triggers the extracellular shuttling and downregulation of LARP7, which dampens SIRT1 deacetylase activity, enhances p53 and NF-κB (p65) transcriptional activity by augmenting their acetylation, and thereby accelerates cellular senescence. Deletion of LARP7 leads to senescent cell accumulation and premature aging in rodent model. Furthermore, we show this ATM-LARP7-SIRT1-p53/p65 senescence axis is active in vascular senescence and atherogenesis, and preventing its activation substantially alleviates senescence and atherogenesis. Together, this study identifies LARP7 as a gatekeeper of senescence, and the altered ATM-LARP7-SIRT1-p53/p65 pathway plays an important role in DNA damage response (DDR)-mediated cellular senescence and atherosclerosis.

Keywords: DNA damage; LARP7; aging; atherosclerosis; senescence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Aging / metabolism
  • Aging / physiology
  • Animals
  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • Cell Line, Tumor
  • Cellular Senescence / physiology*
  • DNA Damage
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Oxidative Stress / genetics
  • RNA-Binding Proteins / metabolism
  • RNA-Binding Proteins / physiology
  • Ribonucleoproteins / metabolism*
  • Ribonucleoproteins / physiology
  • Signal Transduction
  • Sirtuin 1 / metabolism*
  • Sirtuin 1 / physiology
  • Transcription Factor RelA / metabolism
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Larp7 protein, human
  • Larp7 protein, mouse
  • RNA-Binding Proteins
  • Ribonucleoproteins
  • Transcription Factor RelA
  • Tumor Suppressor Protein p53
  • Ataxia Telangiectasia Mutated Proteins
  • SIRT1 protein, human
  • Sirt1 protein, mouse
  • Sirtuin 1