論文

査読有り
2014年6月

PPARβ/δ activation of CD300a controls intestinal immunity

Scientific Reports
  • 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, Gonzalez
  • Atsushi, Nakajima
  • Hiroyuki, Aburatani
  • Makoto, Naito
  • Akira, Shibuya
  • Tatsuhiko, Kodama
  • Sakai, Juro
  • 全て表示

4
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/srep05412
出版者・発行元
NATURE PUBLISHING GROUP

Macrophages are important for maintaining intestinal immune homeostasis. Here, we show that PPAR beta/delta (peroxisome proliferator-activated receptor beta/delta) 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.

リンク情報
DOI
https://doi.org/10.1038/srep05412
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000337889300002&DestApp=WOS_CPL
ID情報
  • DOI : 10.1038/srep05412
  • ISSN : 2045-2322
  • Web of Science ID : WOS:000337889300002

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