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脂肪组织不变自然杀伤 T 细胞通过调节细胞因子的产生来预防饮食诱导的肥胖和代谢紊乱。

Adipose tissue invariant NKT cells protect against diet-induced obesity and metabolic disorder through regulatory cytokine production.

机构信息

Hematology/Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

出版信息

Immunity. 2012 Sep 21;37(3):574-87. doi: 10.1016/j.immuni.2012.06.016. Epub 2012 Sep 13.

Abstract

Invariant natural killer T (iNKT) cells are evolutionarily conserved innate T cells that influence inflammatory responses. We have shown that iNKT cells, previously thought to be rare in humans, were highly enriched in human and murine adipose tissue, and that as adipose tissue expanded in obesity, iNKT cells were depleted, correlating with proinflammatory macrophage infiltration. iNKT cell numbers were restored in mice and humans after weight loss. Mice lacking iNKT cells had enhanced weight gain, larger adipocytes, fatty livers, and insulin resistance on a high-fat diet. Adoptive transfer of iNKT cells into obese mice or in vivo activation of iNKT cells via their lipid ligand, alpha-galactocylceramide, decreased body fat, triglyceride levels, leptin, and fatty liver and improved insulin sensitivity through anti-inflammatory cytokine production by adipose-derived iNKT cells. This finding highlights the potential of iNKT cell-targeted therapies, previously proven to be safe in humans, in the management of obesity and its consequences.

摘要

不变自然杀伤 T(iNKT)细胞是进化上保守的先天 T 细胞,可影响炎症反应。我们已经表明,先前被认为在人类中很少见的 iNKT 细胞在人和鼠的脂肪组织中高度富集,并且随着肥胖时脂肪组织的扩张,iNKT 细胞被耗尽,与促炎巨噬细胞浸润相关。减肥后,iNKT 细胞的数量在小鼠和人类中得到了恢复。缺乏 iNKT 细胞的小鼠在高脂肪饮食中体重增加更多、脂肪细胞更大、脂肪肝和胰岛素抵抗增强。将 iNKT 细胞过继转移到肥胖小鼠中,或通过其脂质配体α-半乳糖神经酰胺在体内激活 iNKT 细胞,可减少体脂肪、甘油三酯水平、瘦素和脂肪肝,并通过脂肪组织来源的 iNKT 细胞产生抗炎细胞因子来改善胰岛素敏感性。这一发现强调了 iNKT 细胞靶向治疗的潜力,此前在人类中已被证明是安全的,可用于肥胖及其后果的管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f346/4991771/1221726544fb/nihms404513f1.jpg

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