The aging mouse lipidome
Esparza, E.; Pilley, S. E.; Shi, X.; Iyengar, P.; Sivaraman, S.; Wang, G.; Mulondo, R.; Kashyap, S. B.; Moaddeli, D.; Coakley, A. J.; Higuchi-Sanabria, R.; Cohn, W.; Mullen, P. J.
Show abstract
Aging is associated with widespread metabolic changes that contribute to functional decline and disease. While prior studies have characterized age-associated changes in lipids, it still remains incompletely understood how the lipidome changes across tissues and between sexes during aging. Here, we performed targeted lipidomics across 10 organs collected from male and female mice at five ages spanning adolescence to old age. We analyzed 775 lipids across multiple lipid classes and found that aging affects the lipidome in an organ-specific manner. The thymus and quadriceps muscle had the most age-associated lipid changes, whereas lipid levels in organs such as the kidney and lung remained more stable. In quadriceps muscle, aging was associated with a decrease in specific phosphatidylcholine and phosphatidylethanolamine lipids, particularly those containing adrenic acid. We also identified sex-dependent differences in lipid composition, with the spleen showing differences throughout life. Spleens from female mice had lower levels of lysophosphatidylcholine and lysophosphatidylethanolamine compared to males. Together, these data provide a comprehensive atlas of age- and sex-associated lipid changes across mouse organs and complement existing metabolic and transcriptomic resources to support studies of mouse aging.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Aging-related inflammation driven by cellular senescence enhances NAD consumption via activation of CD38+ macrophages 96%
- Sexual dimorphism and the multi-omic response to exercise training in rat subcutaneous white adipose tissue 94%
- Gut Microbiome Pattern Reflects Healthy Aging and Predicts Extended Survival in Humans 94%
Similar papers in this journal
- Mitochondrial interactome remodeling in aging mouse skeletal muscle associated with functional decline. 96%
- GDF3 promotes adipose tissue macrophage-mediated inflammation via altered chromatin accessibility during aging 96%
- Nerve-associated macrophages control adipose homeostasis across lifespan and restrain age-related inflammation 96%
Similar papers in this journal
- Alterations of the gut microbiome are associated with epigenetic age acceleration and physical fitness 96%
- Exercise is associated with younger methylome and transcriptome profiles in human skeletal muscle 95%
- Rapamycin Reverses the Hepatic Response to Diet-Induced Metabolic Stress That Is Amplified by Aging. 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.