| First Author | Kang S | Year | 2018 |
| Journal | Nat Immunol | Volume | 19 |
| Issue | 6 | Pages | 561-570 |
| PubMed ID | 29777213 | Mgi Jnum | J:282540 |
| Mgi Id | MGI:6381232 | Doi | 10.1038/s41590-018-0108-0 |
| Citation | Kang S, et al. (2018) Semaphorin 6D reverse signaling controls macrophage lipid metabolism and anti-inflammatory polarization. Nat Immunol 19(6):561-570 |
| abstractText | 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 gamma (PPARgamma) axis plays critical roles in macrophage polarization. Inhibition of mTOR or loss of Sema6D blocked anti-inflammatory macrophage polarization, concomitant with severe impairments in PPARgamma 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 PPARgamma 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 PPARgamma. |
