Division of Endocrinology, Diabetes & Metabolism, Children's Hospital Los Angeles, California, USA.
Obesity (Silver Spring). 2013 Jul;21(7):1380-8. doi: 10.1002/oby.20159. Epub 2013 Jun 11.
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.
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.
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-α. However, obesity did not impair glucose tolerance in the NSG mice.
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.
浸润脂肪组织并分泌促炎细胞因子的巨噬细胞可能是导致肥胖引起的胰岛素抵抗的原因。然而,尽管一些研究表明这可能受到 T 和 B 淋巴细胞的调节,但巨噬细胞为何迁移到脂肪组织并被激活的原因仍不清楚。在这项研究中,我们测试了 T 和 B 淋巴细胞以及自然杀伤 (NK) 细胞是否是肥胖引起脂肪组织中巨噬细胞活化所必需的。
NOD/SCID/IL2-受体 γ 链敲除 (NSG) 小鼠由于缺乏成熟的 T 和 B 淋巴细胞和 NK 细胞,通过选择性减少产仔数并在高脂肪饮食中断奶而肥胖。然后,将这些小鼠维持在该饮食中 10-11 周。
肥胖的 NSG 小鼠的脂肪组织中存在更多的活化巨噬细胞,而非肥胖小鼠。这些巨噬细胞存在于围绕脂肪细胞的“冠状结构”中,并且表达更高水平的炎症细胞因子 TNF-α。然而,肥胖并未损害 NSG 小鼠的葡萄糖耐量。
这些研究表明,T 和 B 淋巴细胞以及 NK 细胞不是肥胖小鼠脂肪组织中巨噬细胞活化所必需的。T 和 B 淋巴细胞和/或 NK 细胞可能是肥胖引起的葡萄糖耐量受损所必需的。