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Vitamin D Modulates Lipid Composition of Adipocyte-Derived Extracellular Vesicles Under Inflammatory Conditions. | LitMetric

AI Article Synopsis

  • - This study investigates how vitamin D (VD) affects the lipid composition of extracellular vesicles derived from adipocytes (AdEVs), which can influence energy balance and inflammation.
  • - Research using a specialized approach (LC-MS/MS) identifies differences in lipid types between small (sEVs) and large extracellular vesicles (lEVs), showing that VD alters lipid profiles, especially under inflammation.
  • - The findings suggest that VD, both independently and during inflammatory responses, creates a distinct lipid signature in AdEVs, supporting its role in reducing inflammation.

Article Abstract

Scope: Adipocyte-derived extracellular vesicles (AdEVs) convey lipids that can play a role in the energy homeostasis. Vitamin D (VD) has been shown to limit the metabolic inflammation as it decreases inflammatory markers expression in adipose tissue (AT). However, VD effect on adipocytes-derived EVs has never been investigated.

Methods And Results: Thus, the aim of this study is to evaluate the AdEVs lipid composition by LC-MS/MS approach in 3T3-L1 cells treated with VD or/and pro-inflammatory factor (tumor necrosis factor α [TNFα]). Among all lipid species, four are highlighted (glycerolipids, phospholipids, lysophospholipids, and sphingolipids) with a differential content between small (sEVs) and large EVs (lEVs). This study also observes that VD alone modulates EV lipid species involved in membrane fluidity and in the budding of membrane. EVs treated with VD under inflammatory conditions have different lipid profiles than the control group, which is more pronounced in lEVs. Indeed, 25 lipid species are significantly modulated in lEVs, compared with only seven lipid species in sEVs.

Conclusions: This study concludes that VD, alone or under inflammatory conditions, is associated with specific lipidomic signature of sEVs and lEVs. These observations reinforce current knowledge on the anti-inflammatory effect of VD.

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Source
http://dx.doi.org/10.1002/mnfr.202300374DOI Listing

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