Lynch, Lydia, Nowak, Michael, Varghese, Bindu, Clark, Justice, Hogan, Andrew E., Toxavidis, Vasillis, Balk, Steven P., O'Shea, Donal, O'Farrelly, Cliona and Exley, Mark A. (2012) Adipose Tissue Invariant NKT Cells Protect against Diet-Induced Obesity and Metabolic Disorder through Regulatory Cytokine Production. Immunity, 37 (3). pp. 574-587. ISSN 1097-4180
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Abstract
Invariant natural killer T (iNKT) cells are evolutionarily
conserved innate T cells that influence inflammatory
responses. We have shown that iNKT cells, previously thought to be rare in humans, were highly enriched in human and murine adipose tissue, and
that as adipose tissue expanded in obesity, iNKT
cells were depleted, correlating with proinflammatory macrophage infiltration. iNKT cell numbers
were restored in mice and humans after weight
loss. Mice lacking iNKT cells had enhanced weight
gain, larger adipocytes, fatty livers, and insulin resistance on a high-fat diet. Adoptive transfer of iNKT
cells into obese mice or in vivo activation of iNKT
cells via their lipid ligand, alpha-galactocylceramide,
decreased body fat, triglyceride levels, leptin, and
fatty liver and improved insulin sensitivity through
anti-inflammatory cytokine production by adiposederived iNKT cells. This finding highlights the potential of iNKT cell-targeted therapies, previously proven
to be safe in humans, in the management of obesity
and its consequences.
Item Type: | Article |
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Keywords: | Adipose Tissue; Invariant; NKT Cells; Diet-Induced Obesity; Metabolic Disorder; Regulatory Cytokine Production; |
Academic Unit: | Faculty of Science and Engineering > Biology |
Item ID: | 12431 |
Identification Number: | 10.1016/j.immuni.2012.06.016 |
Depositing User: | Andrew Hogan |
Date Deposited: | 17 Feb 2020 15:54 |
Journal or Publication Title: | Immunity |
Publisher: | Elsevier |
Refereed: | Yes |
Related URLs: | |
URI: | https://mural.maynoothuniversity.ie/id/eprint/12431 |
Use Licence: | This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here |
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