The State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, 21 Sassoon Road, Laboratory Block, Pokfulam, Hong Kong, China; Department of Medicine, The University of Hong Kong, Hong Kong, China.
The Key Laboratory of Regenerative Biology, Guangzhou Institute of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China.
Cell Metab. 2017 Sep 5;26(3):493-508.e4. doi: 10.1016/j.cmet.2017.08.003. Epub 2017 Aug 24.
Type 2 cytokines are important signals triggering biogenesis of thermogenic beige adipocytes in white adipose tissue (WAT) during cold acclimation. However, how cold activates type 2 immunity in WAT remains obscure. Here we show that cold-induced type 2 immune responses and beiging in subcutaneous WAT (scWAT) are abrogated in mice with adipose-selective ablation of FGF21 or its co-receptor β-Klotho, whereas such impairments are reversed by replenishment with chemokine CCL11. Mechanistically, FGF21 acts on adipocytes in an autocrine manner to promote the expression and secretion of CCL11 via activation of ERK1/2, which drives recruitment of eosinophils into scWAT, leading to increases in accumulation of M2 macrophages, and proliferation and commitment of adipocyte precursors into beige adipocytes. These FGF21-elicited type 2 immune responses and beiging are blocked by CCL11 neutralization. Thus, the adipose-derived FGF21-CCL11 axis triggers cold-induced beiging and thermogenesis by coupling sympathetic nervous system to activation of type 2 immunity in scWAT.
2 型细胞因子是在冷适应过程中触发白色脂肪组织(WAT)中产热米色脂肪细胞发生生物发生的重要信号。然而,冷如何激活 WAT 中的 2 型免疫仍然不清楚。在这里,我们表明,在脂肪组织特异性敲除 FGF21 或其共同受体β-Klotho 的小鼠中,冷诱导的 2 型免疫反应和米色化在皮下 WAT(scWAT)中被阻断,而用趋化因子 CCL11 补充则逆转了这种损伤。在机制上,FGF21 以自分泌方式作用于脂肪细胞,通过激活 ERK1/2 促进 CCL11 的表达和分泌,从而驱动嗜酸性粒细胞进入 scWAT,导致 M2 巨噬细胞的积累增加,以及脂肪细胞前体增殖并向米色脂肪细胞分化。这些由 FGF21 引发的 2 型免疫反应和米色化被 CCL11 中和阻断。因此,脂肪组织来源的 FGF21-CCL11 轴通过将交感神经系统与 scWAT 中 2 型免疫的激活偶联,触发冷诱导的米色化和产热。