Adipose tissue invariant NKT cells protect against diet-induced obesity and metabolic disorder through regulatory cytokine production.
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Authors
Lynch, LydiaNowak, Michael
Varghese, Bindu
Clark, Justice
Hogan, Andrew E
Toxavidis, Vasillis
Balk, Steven P
O'Shea, Donal
O'Farrelly, Cliona
Exley, Mark A
Affiliation
Hematology/Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA. llynch1@bidmc.harvard.eduIssue Date
2012-09-21MeSH
Adipose TissueAdoptive Transfer
Adult
Animals
Antigens, CD11c
Antigens, CD1d
Cytokines
Diet, High-Fat
Female
Flow Cytometry
Humans
Liver
Lymphocyte Count
Macrophages
Male
Metabolic Diseases
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Obese
Middle Aged
Natural Killer T-Cells
Obesity
Spleen
Young Adult
Metadata
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Adipose tissue invariant NKT cells protect against diet-induced obesity and metabolic disorder through regulatory cytokine production. 2012, 37 (3):574-87 ImmunityPublisher
ImmunityJournal
ImmunityDOI
10.1016/j.immuni.2012.06.016PubMed ID
22981538Abstract
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 adipose-derived 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
ArticleLanguage
enISSN
1097-4180ae974a485f413a2113503eed53cd6c53
10.1016/j.immuni.2012.06.016