Heart of the matter: Mitochondrial dynamics and genome alterations in cardiac aging

Claudie Gabillard-Lefort1, Théophile Thibault1, Guy Lenaers2

  • 1University of Angers, MitoLab, Unité MITOVASC, UMR CNRS 6015, INSERM U1083, SFR ICAT, Angers, France.

Insights

Mitochondria and their DNA (mtDNA) play key roles in cardiac aging. Mitochondrial dysfunction, including imbalanced dynamics and mtDNA damage, accelerates heart aging and promotes inflammation.

Area of Science:

  • Cardiology
  • Mitochondrial Biology
  • Gerontology

Background:

  • Cardiovascular diseases are a leading cause of death globally.
  • Cardiac pathological aging is a significant health concern.
  • Mitochondria are vital for heart function and implicated in aging.

Purpose of the Study:

  • To review the pathomechanisms of mitochondrial involvement in cardiac aging.
  • To focus on mitochondrial dynamics and mitochondrial DNA (mtDNA) roles.
  • To explore links between mtDNA, damage, and cellular senescence in the heart.

Main Methods:

  • Literature review of mitochondrial pathomechanisms in cardiac aging.
  • Focus on mitochondrial dynamics (fusion/fission).
  • Analysis of mitochondrial DNA (mtDNA) integrity and release.

Main Results:

  • Imbalanced mitochondrial fusion and fission contribute to aging.
  • Loss of mtDNA integrity causes mitochondrial deficiency.
  • Released mtDNA triggers inflammation via NLRP3, cGAS/STING, and TLR9 pathways.
  • mtDNA damage may link to cardiac senescence.

Conclusions:

  • Mitochondrial dysfunction is central to pathological cardiac aging.
  • Understanding these mechanisms can guide therapies for healthy aging and cardiac repair.

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