B Lymphocytes in obesity-related adipose tissue inflammation and insulin resistance

被引:0
|
作者
Daniel A. Winer
Shawn Winer
Melissa H. Y. Chng
Lei Shen
Edgar G. Engleman
机构
[1] University Health Network,Department of Pathology, Toronto General Hospital
[2] University of Toronto,Division of Cellular and Molecular Biology, Diabetes Research Group, Toronto General Research Institute (TGRI)
[3] University Health Network,Department of Pathology
[4] University of Toronto,undefined
[5] Stanford University School of Medicine,undefined
来源
Cellular and Molecular Life Sciences | 2014年 / 71卷
关键词
Insulin resistance; Type 2 diabetes; B lymphocytes; Inflammation; Autoimmunity; Macrophages; T cells;
D O I
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中图分类号
学科分类号
摘要
Obesity-related insulin resistance is a chronic inflammatory condition that often gives rise to type 2 diabetes (T2D). Much evidence supports a role for pro-inflammatory T cells and macrophages in promoting local inflammation in tissues such as visceral adipose tissue (VAT) leading to insulin resistance. More recently, B cells have emerged as an additional critical player in orchestrating these processes. B cells infiltrate VAT and display functional and phenotypic changes in response to diet-induced obesity. B cells contribute to insulin resistance by presenting antigens to T cells, secreting inflammatory cytokines, and producing pathogenic antibodies. B cell manipulation represents a novel approach to the treatment of obesity-related insulin resistance and potentially to the prevention of T2D. This review summarizes the roles of B cells in governing VAT inflammation and the mechanisms by which these cells contribute to altered glucose homeostasis in insulin resistance.
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页码:1033 / 1043
页数:10
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