PPARβ/δ activation of CD300a controls intestinal immunity

PPARβ/δ激活CD300a调控肠道免疫

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作者:Toshiya Tanaka,Satoko Tahara-Hanaoka,Tsukasa Nabekura,Kaori Ikeda,Shuying Jiang,Shuichi Tsutsumi,Takeshi Inagaki,Kenta Magoori,Takuma Higurashi,Hirokazu Takahashi,Keisuke Tachibana,Yuya Tsurutani,Sana Raza,Motonobu Anai,Takashi Minami,Youichiro Wada,Koutaro Yokote,Takefumi Doi,Takao Hamakubo,Johan Auwerx,Frank J Gonzalez,Atsushi Nakajima,Hiroyuki Aburatani,Makoto Naito,Akira Shibuya,Tatsuhiko Kodama,Juro Sakai

Abstract

Macrophages are important for maintaining intestinal immune homeostasis. Here, we show that PPARβ/δ (peroxisome proliferator-activated receptor β/δ) directly regulates CD300a in macrophages that express the immunoreceptor tyrosine based-inhibitory motif (ITIM)-containing receptor. In mice lacking CD300a, high-fat diet (HFD) causes chronic intestinal inflammation with low numbers of intestinal lymph capillaries and dramatically expanded mesenteric lymph nodes. As a result, these mice exhibit triglyceride malabsorption and reduced body weight gain on HFD. Peritoneal macrophages from Cd300a-/- mice on HFD are classically M1 activated. Activation of toll-like receptor 4 (TLR4)/MyD88 signaling by lipopolysaccharide (LPS) results in prolonged IL-6 secretion in Cd300a-/- macrophages. Bone marrow transplantation confirmed that the phenotype originates from CD300a deficiency in leucocytes. These results identify CD300a-mediated inhibitory signaling in macrophages as a critical regulator of intestinal immune homeostasis.

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