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.
Abstract:
Cardiac pathological aging is a serious health issue, with cardiovascular diseases still being a leading cause of deaths worldwide. Therefore, there is an urgent need to identify culprit factors involved in this process. In the last decades, mitochondria, which are crucial for cardiac function, have emerged as major contributors. Mitochondria are organelles involved in a plethora of metabolic pathways and cell processes ranging from ATP production to calcium homeostasis or regulation of apoptotic pathways. This review provides a general overview of the pathomechanisms involving mitochondria during cardiac aging, with a focus on the role of mitochondrial dynamics and mitochondrial DNA (mtDNA). These mechanisms involve imbalanced mitochondrial fusion and fission, loss of mtDNA integrity leading to tissue mosaic of mitochondrial deficiency, as well as mtDNA release in the cytoplasm, promoting inflammation via the NLRP3, cGAS/STING and TLR9 pathways. Potential links between mtDNA, mitochondrial damage and the accumulation of senescent cells in the heart are also discussed. A better understanding of how these factors impact on heart function and accelerate its pathological aging should lead to the development of new therapies to promote healthy aging and restore age-induced cardiac dysfunction.
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