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固有淋巴细胞在肥胖诱导中的作用。

Innate Lymphoid Cells in the Induction of Obesity.

机构信息

Laboratory for Innate Immune Systems, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan; Laboratory for Immune Cell Systems, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan; Laboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.

Laboratory for Innate Immune Systems, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan; Department of Medical Life Science, Graduate School of Medical Life Science, Yokohama City University, Kanagawa, Japan; Laboratory for Innate Immune Systems, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.

出版信息

Cell Rep. 2019 Jul 2;28(1):202-217.e7. doi: 10.1016/j.celrep.2019.06.016.

Abstract

Complex interactions between immune cells are an important component in the induction of obesity. Here, we show that Il2rgRag2 mice lacking all lymphocytes are resistant to diet-induced obesity. Transplantation of bone marrow cells from Rag2 mice, which lack only acquired immune cells, into Il2rgRag2 mice abolishes this resistance, indicating a role for innate lymphoid cells (ILCs) in this process. Mice lacking ILC2 or ILC3 cells, but not natural killer cells, are resistant to obesity. Adoptive transfer of naive ILC2s isolated from the small intestine (SI), but not ILC2s from white adipose tissue (WAT), restores the induction of diet-induced obesity in Il2rgRag2 mice. Analysis of transcriptional differences reveals that SI-ILC2s express higher levels of IL-2 than do WAT-ILC2s and that blockade of IL-2 signaling impairs weight gain and reduces the populations of ILC2s and ILC3s in the SI, suggesting a role for the IL-2/ILC2/3 axis in the induction of obesity.

摘要

免疫细胞之间的复杂相互作用是诱导肥胖的一个重要组成部分。在这里,我们表明缺乏所有淋巴细胞的 Il2rgRag2 小鼠对饮食诱导的肥胖具有抗性。将仅缺乏获得性免疫细胞的 Rag2 小鼠的骨髓细胞移植到 Il2rgRag2 小鼠中,会消除这种抗性,表明先天淋巴细胞 (ILC) 在这个过程中起作用。缺乏 ILC2 或 ILC3 细胞但不缺乏自然杀伤细胞的小鼠对肥胖具有抗性。从小肠 (SI) 分离的幼稚 ILC2 的过继转移,但不是来自白色脂肪组织 (WAT) 的 ILC2,可恢复 Il2rgRag2 小鼠中饮食诱导的肥胖的诱导。转录差异分析表明,SI-ILC2 比 WAT-ILC2 表达更高水平的 IL-2,而阻断 IL-2 信号会损害体重增加并减少 SI 中的 ILC2 和 ILC3 细胞群,表明 IL-2/ILC2/3 轴在肥胖的诱导中起作用。

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