| Literature DB >> 33355987 |
Stephanie Lazo1, Nicole Noren Hooten1, Jamal Green1, Erez Eitan2, Nicolle A Mode1, Qing-Rong Liu3, Alan B Zonderman1, Ngozi Ezike1, Mark P Mattson2, Paritosh Ghosh3, Michele K Evans1.
Abstract
The mitochondrial free radical theory of aging suggests that accumulating oxidative damage to mitochondria and mitochondrial DNA (mtDNA) plays a central role in aging. Circulating cell-free mtDNA (ccf-mtDNA) isolated from blood may be a biomarker of disease. Extracellular vesicles (EVs) are small (30-400 nm), lipid-bound vesicles capable of shuttling proteins, nucleic acids, and lipids as part of intercellular communication systems. Here, we report that a portion of ccf-mtDNA in plasma is encapsulated in EVs. To address whether EV mtDNA levels change with human age, we analyzed mtDNA in EVs from individuals aged 30-64 years cross-sectionally and longitudinally. EV mtDNA levels decreased with age. Furthermore, the maximal mitochondrial respiration of cultured cells was differentially affected by EVs from old and young donors. Our results suggest that plasma mtDNA is present in EVs, that the level of EV-derived mtDNA is associated with age, and that EVs affect mitochondrial energetics in an EV age-dependent manner. Published 2020. This article is a US Government work and is in the public domain in the USA.Entities:
Keywords: aging; biomarker; circulating cell-free mitochondrial DNA; exosomes; extracellular vesicles; intercellular communication; microvesicles; mitochondrial DNA
Year: 2020 PMID: 33355987 PMCID: PMC7811845 DOI: 10.1111/acel.13283
Source DB: PubMed Journal: Aging Cell ISSN: 1474-9718 Impact factor: 9.304