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Lipoxins reduce obesity-induced adipose tissue inflammation in 3D-cultured human adipocytes and explant cultures

Adipose tissue inflammation drives obesity-related cardiometabolic diseases. Enhancing endogenous resolution mechanisms through administration of lipoxin A(4), a specialized pro-resolving lipid mediator, was shown to reduce adipose inflammation and subsequently protects against obesity-induced syste...

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Detalles Bibliográficos
Autores principales: Soták, Matúš, Rajan, Meenu Rohini, Clark, Madison, Harms, Matthew, Rani, Alankrita, Kraft, Jamie D., Tandio, David, Shen, Tong, Borkowski, Kamil, Fiehn, Oliver, Newman, John W., Quiding-Järbrink, Marianne, Biörserud, Christina, Apelgren, Peter, Staalesen, Trude, Hagberg, Carolina E., Boucher, Jeremie, Wallenius, Ville, Lange, Stephan, Börgeson, Emma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249816/
https://www.ncbi.nlm.nih.gov/pubmed/35789845
http://dx.doi.org/10.1016/j.isci.2022.104602
Descripción
Sumario:Adipose tissue inflammation drives obesity-related cardiometabolic diseases. Enhancing endogenous resolution mechanisms through administration of lipoxin A(4), a specialized pro-resolving lipid mediator, was shown to reduce adipose inflammation and subsequently protects against obesity-induced systemic disease in mice. Here, we demonstrate that lipoxins reduce inflammation in 3D-cultured human adipocytes and adipose tissue explants from obese patients. Approximately 50% of patients responded particularly well to lipoxins by reducing inflammatory cytokines and promoting an anti-inflammatory M2 macrophage phenotype. Responding patients were characterized by elevated systemic levels of C-reactive protein, which causes inflammation in cultured human adipocytes. Responders appeared more prone to producing anti-inflammatory oxylipins and displayed elevated prostaglandin D2 levels, which has been interlinked with transcription of lipoxin-generating enzymes. Using explant cultures, this study provides the first proof-of-concept evidence supporting the therapeutic potential of lipoxins in reducing human adipose tissue inflammation. Our data further indicate that lipoxin treatment may require a tailored personalized-medicine approach.