T Cell Activation Inhibitors Reduce CD8+T Cell and Pro-Inflammatory Macrophage Accumulation in Adipose Tissue of Obese Mice

被引:36
|
作者
Montes, Vince N. [1 ]
Turner, Michael S. [2 ]
Subramanian, Savitha [1 ]
Ding, Yilei [1 ]
Hayden-Ledbetter, Martha [3 ]
Slater, Sonya [3 ]
Goodspeed, Leela [1 ]
Wang, Shari [1 ]
Omer, Mohamed [1 ]
Den Hartigh, Laura J. [1 ]
Averill, Michelle M. [1 ]
O'Brien, Kevin D. [4 ]
Ledbetter, Jeffrey [3 ]
Chait, Alan [1 ]
机构
[1] Univ Washington, Div Metab Endocrinol & Nutr, Seattle, WA 98195 USA
[2] Benaroya Res Inst, Seattle, WA USA
[3] Univ Washington, Div Rheumatol, Seattle, WA 98195 USA
[4] Univ Washington, Div Cardiol, Seattle, WA 98195 USA
来源
PLOS ONE | 2013年 / 8卷 / 07期
关键词
DIET-INDUCED OBESITY; SERUM AMYLOID A3; INSULIN-RESISTANCE; LDL RECEPTOR; ATHEROSCLEROSIS; PATHOPHYSIOLOGY; APOLIPOPROTEIN; IMMUNOGLOBULIN; COSTIMULATION; CHOLESTEROL;
D O I
10.1371/journal.pone.0067709
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adipose tissue inflammation and specifically, pro-inflammatory macrophages are believed to contribute to insulin resistance (IR) in obesity in humans and animal models. Recent studies have invoked T cells in the recruitment of pro-inflammatory macrophages and the development of IR. To test the role of the T cell response in adipose tissue of mice fed an obesogenic diet, we used two agents (CTLA-4 Ig and anti-CD40L antibody) that block co-stimulation, which is essential for full T cell activation. C57BL/6 mice were fed an obesogenic diet for 16 weeks, and concomitantly either treated with CTLA-4 Ig, anti-CD40L antibody or an IgG control (300 mu g/week). The treatments altered the immune cell composition of adipose tissue in obese mice. Treated mice demonstrated a marked reduction in pro-inflammatory adipose tissue macrophages and activated CD8+ T cells. Mice treated with anti-CD40L exhibited reduced weight gain, which was accompanied by a trend toward improved IR. CTLA-4 Ig treatment, however, was not associated with improved IR. These data suggest that the presence of pro-inflammatory T cells and macrophages can be altered with co-stimulatory inhibitors, but may not be a significant contributor to the whole body IR phenotype.
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页数:13
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