| Literature DB >> 36266352 |
Meric Erikci Ertunc1, Pan Zhang2, Dan Tan1, Srihari Konduri3, Justin Wang1, Tina Chang1, Antonio F M Pinto1, Andrea Rocha1, Cynthia J Donaldson1, Joan M Vaughan1, Raissa G Ludwig4, Elizabeth Willey5, Manasi Iyer6, Peter C Gray1, Pamela Maher7, Nicola J Allen8, J Bradley Zuchero6, Andrew Dillin5, Marcelo A Mori4, Steven G Kohama9, Dionicio Siegel10, Alan Saghatelian11.
Abstract
Lipids contribute to the structure, development, and function of healthy brains. Dysregulated lipid metabolism is linked to aging and diseased brains. However, our understanding of lipid metabolism in aging brains remains limited. Here we examined the brain lipidome of mice across their lifespan using untargeted lipidomics. Co-expression network analysis highlighted a progressive decrease in 3-sulfogalactosyl diacylglycerols (SGDGs) and SGDG pathway members, including the potential degradation products lyso-SGDGs. SGDGs show an age-related decline specifically in the central nervous system and are associated with myelination. We also found that an SGDG dramatically suppresses LPS-induced gene expression and release of pro-inflammatory cytokines from macrophages and microglia by acting on the NF-κB pathway. The detection of SGDGs in human and macaque brains establishes their evolutionary conservation. This work enhances interest in SGDGs regarding their roles in aging and inflammatory diseases and highlights the complexity of the brain lipidome and potential biological functions in aging.Entities:
Year: 2022 PMID: 36266352 DOI: 10.1038/s41589-022-01165-6
Source DB: PubMed Journal: Nat Chem Biol ISSN: 1552-4450 Impact factor: 16.174