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ABSTRACT: Background
Aging enhances most chronic diseases but its impact on human aortic tissue in health and in thoracic aortic aneurysms (TAA) remains unclear.Methods
We employed a human aortic biorepository of healthy specimens (n=17) and those that underwent surgical repair for TAA (n=20). First, we performed proteomics comparing aortas of healthy donors to aneurysmal specimens, in young (ie, <60 years of age) and old (ie, ≥60 years of age) subjects. Second, we measured proteins, via immunoblotting, involved in mitophagy (ie, Parkin) and also mitochondrial-induced inflammatory pathways, specifically TLR (toll-like receptor) 9, STING (stimulator of interferon genes), and IFN (interferon)-β.Results
Proteomics revealed that aging transformed the aorta both quantitatively and
SUBMITTER: Tyrrell DJ
PROVIDER: S-EPMC9339483 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature