期刊
OBESITY
卷 21, 期 7, 页码 1380-1388出版社
WILEY
DOI: 10.1002/oby.20159
关键词
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资金
- National Cancer Institute [CA139060]
- TJ Martell Foundation
- Children's Cancer Research Fund, a California non-profit organization
Objective: Macrophages which infiltrate adipose tissue and secrete proinflammatory cytokines may be responsible for obesity-induced insulin resistance. However, the reason why macrophages migrate into adipose tissue and become activated remains unknown though some studies suggest that this may be regulated by T and B lymphocytes. In this study, it has been tested whether T and B lymphocytes and natural killer (NK) cells were necessary for the obesity-induced activation of macrophages in adipose tissue. Design and Methods: NOD/SCID/IL2-receptor gamma-chain knockout (NSG) mice, which lack mature T and B lymphocytes and NK cells, were made obese by selectively reducing litters and weaning onto a high-fat diet. Mice were then maintained on the diet for 10-11 weeks. Results: Adipose tissue from obese NSG mice had more activated macrophages than nonobese mice. These macrophages were found in crown-like structures'' surrounding adipocytes, and expressed higher levels of the inflammatory cytokine TNF-alpha. However, obesity did not impair glucose tolerance in the NSG mice. Conclusions: These studies demonstrated that T and B lymphocytes and NK cells are not necessary for adipose tissue macrophage activation in obese mice. T and B lymphocytes and/or NK cells may be necessary for the development of obesity-induced impaired glucose tolerance.
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