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RESEARCH PAPER / 2026-01-22

Mitochondrial DNA is an important signaling molecule in cardiovascular aging and pathophysiology.

Yutao Hua, Yuxin Chu, Sarah Fu, Armaan Verma, Jianhua Zhang, Palaniappan Sethu, Timmy Lee, Min Xie

Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35233. · pubmed

Abstract

Mitochondrial DNA (mtDNA) has emerged as a key signaling molecule, extending beyond its primary role in supporting energy production. Its replication, release, and degradation are tightly regulated, and their dysregulation can activate immune pathways, including TLR9, cGAS-STING, and inflammasomes. In this review, we summarize recent advances in understanding mtDNA biology, including mechanisms of replication and release, recognition by pattern recognition receptors, and its impact on disease. We highlight evidence linking mtDNA to cardiovascular disease, as well as the aging-related chronic kidney disease, lung disorders, and neurodegeneration, and discuss the utility of circulating mtDNA copy number as a biomarker. Finally, we outline therapeutic strategies to reduce mtDNA release, block its sensing, and enhance clearance via autophagy/mitophagy. These findings underscore mtDNA as both a driver of pathology and a promising target for diagnosis and therapy across multiple organ systems.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

Mitochondrial DNA serves as a signaling molecule that influences cardiovascular aging and related pathophysiological processes. The paper is relevant as it explores mechanisms that could address root causes of aging and their systemic effects, rather than merely treating age-related diseases.

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