Lymphocyte roles in metabolic dysfunction: of men and mice

被引:44
作者
Ip, Blanche C. [1 ]
Hogan, Andrew E. [2 ]
Nikolajczyk, Barbara S. [1 ,3 ]
机构
[1] Boston Univ, Dept Microbiol, Boston, MA 02215 USA
[2] Univ Coll Dublin, St Vincents Univ Hosp, Educ & Res Ctr, Obes Immunol Grp, Dublin, Ireland
[3] Boston Univ, Dept Med, Boston, MA USA
基金
美国国家卫生研究院;
关键词
insulin resistance; type; 2; diabetes; obesity; lymphocyte subsets; REGULATORY T-CELLS; ADIPOSE-TISSUE INFLAMMATION; INVARIANT NKT CELLS; ROR-GAMMA-T; INSULIN-RESISTANCE; NATURAL-KILLER; PERIPHERAL-BLOOD; HEPATIC STEATOSIS; INTERLEUKIN; 22; T(H)17 CELLS;
D O I
10.1016/j.tem.2014.12.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type 2 diabetes (T2D) is a metabolic disease associated with obesity-related insulin resistance (IR) and chronic inflammation. Animal studies indicate that IR can be caused and/or exacerbated by systemic and/or tissue-specific alterations in lymphocyte differentiation and function. Human studies also indicate that obesity-associated inflammation promotes IR. Nevertheless, clinical trials with anti-inflammatory therapies have yielded modest impacts on established T2D. Unlike mouse models, where obesity is predominantly associated with IR, 20-25% of obese humans are metabolically healthy with high insulin sensitivity. The uncoupling of obesity from IR in humans but not in animal models advocates for a more comprehensive understanding of mediators and mechanisms of human obesity-promoted IR, and better integration of knowledge from human studies into animal experiments to efficiently pursue T2D prevention and treatment.
引用
收藏
页码:91 / 100
页数:10
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