Natural aging drives a subclinical cardiovascular phenotype in a non-human primate
Klösener, L.; Samak, M.; Lerm, D.; Ye, J. L.; Bleckwedel, F.; Moussavi, A.; Memhave, T. R.; Ramedani, M.; Ramos Gomes, F.; Khan, A.; Kulkarni, A.; Sitte, M.; Salinas, G.; König, J.; Möbius, W.; Sadowski, B.; Steffens, S.; Kunz, M.; Zelarayan, L.; Lenz, C.; Bär, C.; Behr, R.; Boretius, S.; Alves, F.; Thum, T.; Germena, G.; Mietsch, M.; Hinkel, R.
Show abstract
Aging is an inevitable risk factor for cardiovascular disease. Profound understanding of mechanisms underlying the early stages of cardiovascular aging is essential for the development of novel therapeutics. Therefore, animal models which closely reflect the human condition are highly sought after. Here, we investigated natural cardiovascular aging in a non-human primate, comparing healthy young-adult and aged common marmosets (Callithrix jacchus). Despite preservation of most cardiac functional parameters in aged animals, significant histological alterations were found including fibrosis and microvascular rarefaction. Molecular phenotyping by single-nuclei RNA-sequencing revealed activation of cardiac stress, pro-inflammatory and fibrotic gene programs in aged hearts. Importantly, proteomic analysis of cardiac extracellular vesicles revealed a cardioprotective cargo in young animals while functionally demonstrating pro-angiogenic properties on human cardiac microvascular endothelial cells. Finally, large vessel atherosclerosis was strikingly evident in aged animals and elucidated by bulk RNA-sequencing. Overall, the aging marmoset offers a great potential for translational cardiovascular research.
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