Key result
Obesity altered the mouse adipose extracellular vesicle lipidome, mirroring lipid alterations in plasma and visceral adipose tissue, with enrichment of ceramides and sphingomyelins.
Why the study?
Adipose extracellular vesicles transport lipids that could participate in obesity-related metabolic dysfunctions, prompting the need to define the mouse AdEV lipid signature in healthy and obesity contexts.
AdEV lipid enrichment may contribute to obesity-related dysfunction; leaves open causal roles and therapeutic targeting.
Adipose extracellular vesicles (AdEVs) transport lipids that could participate in the development of obesity-related metabolic dysfunctions. This study aims to define mouse AdEV lipid signature by a targeted LC-MS/MS approach in either healthy or obesity context. Distinct clustering of AdEV and visceral adipose tissue (VAT) lipidomes by principal component analysis reveals specific AdEV lipid sorting when compared with secreting VAT. Comprehensive analysis identifies enrichment of ceramides, sphingomyelins, and phosphatidylglycerols species in AdEVs compared with source VAT whose lipid content closely relates to the obesity status and is influenced by the diet. Obesity moreover impacts AdEV lipidome, mirroring lipid alterations retrieved in plasma and VAT. Overall, our study identifies specific lipid fingerprints for plasma, VAT, and AdEVs that are informative of the metabolic status. Lipid species enriched in AdEVs in the obesity context may constitute biomarker candidates or mediators of the obesity-associated metabolic dysfunctions.
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Blandin et al. (2023) studied Obesity. Obesity vs. Healthy state was evaluated on Adipose extracellular vesicle (AdEV) lipid signature. Obesity altered the mouse adipose extracellular vesicle lipidome, mirroring lipid alterations in plasma and visceral adipose tissue, with enrichment of ceramides and sphingomyelins.
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