Journal Article

Semaphorin 6D reverse signaling controls macrophage lipid metabolism and anti-inflammatory polarization

Kang, Sujin, Koyama, Shohei, Toyofuku, Toshihiko, Nojima, Satoshi, Hayama, Yoshitomo, Nishide, Masayuki, Nakanishi, Yoshimitsu, Kumanogoh, Atsushi, Kinehara, Yuhei, Nakatani, Takeshi, Kimura, Tetsuya, Kato, Yasuhiro, Kioi, Yoshiyuki, Okuzaki, Daisuke, Takamatsu, Hyota, Shimogori, Tomomi, Takagi, Junichi

2018

Overview

Polarization of macrophages into pro-inflammatory or anti-inflammatory states has distinct metabolic requirements, with mechanistic target of rapamycin (mTOR) kinase signaling playing a critical role. However, it remains unclear how mTOR regulates metabolic status to promote polarization of these cells. Here we show that an mTOR–Semaphorin 6D (Sema6D)–Peroxisome proliferator receptor γ (PPARγ) axis plays critical roles in macrophage polarization. Inhibition of mTOR or loss of Sema6D blocked anti-inflammatory macrophage polarization, concomitant with severe impairments in PPARγ expression, uptake of fatty acids, and lipid metabolic reprogramming. Macrophage expression of the receptor Plexin-A4 is responsible for Sema6D-mediated anti-inflammatory polarization. We found that a tyrosine kinase, c-Abl, which associates with the cytoplasmic region of Sema6D, is required for PPARγ expression. Furthermore, Sema6D is important for generation of intestinal resident CX3CR1 hi macrophages and prevents development of colitis. Collectively, these findings highlight crucial roles for Sema6D reverse signaling in macrophage polarization, coupling immunity, and metabolism via PPARγ. Semaphorins play well-known roles in axon guidance. Kumanogoh and colleagues demonstrate that Semaphorin 6D cell-intrinsically activates anti-inflammatory macrophage polarization.

• Publisher: Nature Publishing Group US,Nature Publishing Group
• Subject: 631/250/256 / 692/420/256 / Anti-inflammatory agents / B cells / Biomedical and Life Sciences / Biomedicine / Colitis / Fatty acids / Immunology / Infectious Diseases / Inflammation / Intestine / Lipid metabolism / Macrophages / Medical schools / Metabolism / Phenols (Class of compounds) / Polarization / Protein-tyrosine kinase / Rapamycin / Semaphorins / TOR protein / Tyrosine