| Literature DB >> 29515042 |
Maria Moysidou1,2, Sevasti Karaliota1, Elisavet Kodela1,2, Maria Salagianni1, Yassemi Koutmani1, Antonia Katsouda1, Konstantia Kodella1, Panagiotis Tsakanikas1, Styliani Ourailidou1, Evangelos Andreakos1, Nikolaos Kostomitsopoulos1, Dimitris Skokos3, Antonios Chatzigeorgiou4, Kyoung-Jin Chung4, Stefan Bornstein4, Mark W Sleeman5, Triantafyllos Chavakis4, Katia P Karalis1,4,6.
Abstract
Although accumulation of lymphocytes in the white adipose tissue (WAT) in obesity is linked to insulin resistance, it remains unclear whether lymphocytes also participate in the regulation of energy homeostasis in the WAT. Here, we demonstrate enhanced energy dissipation in Rag1-/- mice, increased catecholaminergic input to subcutaneous WAT, and significant beige adipogenesis. Adoptive transfer experiments demonstrated that CD8+ T cell deficiency accounts for the enhanced beige adipogenesis in Rag1-/- mice. Consistently, we identified that CD8-/- mice also presented with enhanced beige adipogenesis. The inhibitory effect of CD8+ T cells on beige adipogenesis was reversed by blockade of IFN-γ. All together, our findings identify an effect of CD8+ T cells in regulating energy dissipation in lean WAT, mediated by IFN-γ modulation of the abundance of resident immune cells and of local catecholaminergic activity. Our results provide a plausible explanation for the clinical signs of metabolic dysfunction in diseases characterized by altered CD8+ T cell abundance and suggest targeting of CD8+ T cells as a promising therapeutic approach for obesity and other diseases with altered energy homeostasis.Entities:
Keywords: Adipose tissue; Metabolism
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Year: 2018 PMID: 29515042 PMCID: PMC5922290 DOI: 10.1172/jci.insight.95456
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708