Cell type-specific modulation of lipid mediator's formation in murine adipose tissue by omega-3 fatty acids
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26707880
DOI
10.1016/j.bbrc.2015.12.055
PII: S0006-291X(15)31060-3
Knihovny.cz E-zdroje
- Klíčová slova
- Adipose tissue macrophages, Lipid mediators, Lipidomics, Omega-3 PUFA, Protectin D1,
- MeSH
- antiflogistika aplikace a dávkování MeSH
- aplikace orální MeSH
- bílá tuková tkáň cytologie účinky léků imunologie MeSH
- buňky stromatu účinky léků imunologie MeSH
- imunologické faktory imunologie MeSH
- kultivované buňky MeSH
- makrofágy cytologie účinky léků imunologie MeSH
- metabolismus lipidů účinky léků imunologie MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- omega-3 mastné kyseliny aplikace a dávkování MeSH
- potravní doplňky MeSH
- tukové buňky účinky léků enzymologie imunologie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiflogistika MeSH
- imunologické faktory MeSH
- omega-3 mastné kyseliny MeSH
Mutual interactions between adipocytes and immune cells in white adipose tissue (WAT) are involved in modulation of lipid metabolism in the tissue and also in response to omega-3 polyunsaturated fatty acids (PUFA), which counteract adverse effects of obesity. This complex interplay depends in part on in situ formed anti- as well as pro-inflammatory lipid mediators, but cell types engaged in the synthesis of the specific mediators need to be better characterized. We used tissue fractionation and metabolipidomic analysis to identify cells producing lipid mediators in epididymal WAT of mice fed for 5 weeks obesogenic high-fat diet (lipid content 35% wt/wt), which was supplemented or not by omega-3 PUFA (4.3 mg eicosapentaenoic acid and 14.7 mg docosahexaenoic acid per g of diet). Our results demonstrate selective increase in levels of anti-inflammatory lipid mediators in WAT in response to omega-3, reflecting either their association with adipocytes (endocannabinoid-related N-docosahexaenoylethanolamine) or with stromal vascular cells (pro-resolving lipid mediator protectin D1). In parallel, tissue levels of obesity-associated pro-inflammatory endocannabinoids were suppressed. Moreover, we show that adipose tissue macrophages (ATMs), which could be isolated using magnetic force from the stromal vascular fraction, are not the major producers of protectin D1 and that omega-3 PUFA lowered lipid load in ATMs while promoting their less-inflammatory phenotype. Taken together, these results further document specific roles of various cell types in WAT in control of WAT inflammation and metabolism and they suggest that also other cells but ATMs are engaged in production of pro-resolving lipid mediators in response to omega-3 PUFA.
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