| First Author | Bossaller L | Year | 2012 |
| Journal | J Immunol | Volume | 189 |
| Issue | 12 | Pages | 5508-12 |
| PubMed ID | 23144495 | Mgi Jnum | J:190865 |
| Mgi Id | MGI:5449807 | Doi | 10.4049/jimmunol.1202121 |
| Citation | Bossaller L, et al. (2012) Cutting Edge: FAS (CD95) Mediates Noncanonical IL-1beta and IL-18 Maturation via Caspase-8 in an RIP3-Independent Manner. J Immunol 189(12):5508-12 |
| abstractText | Fas, a TNF family receptor, is activated by the membrane protein Fas ligand expressed on various immune cells. Fas signaling triggers apoptosis and induces inflammatory cytokine production. Among the Fas-induced cytokines, the IL-1beta family cytokines require proteolysis to gain biological activity. Inflammasomes, which respond to pathogens and danger signals, cleave IL-1beta cytokines via caspase-1. However, the mechanisms by which Fas regulates IL-1beta activation remain unresolved. In this article, we demonstrate that macrophages exposed to TLR ligands upregulate Fas, which renders them responsive to receptor engagement by Fas ligand. Fas signaling activates caspase-8 in macrophages and dendritic cells, leading to the maturation of IL-1beta and IL-18 independently of inflammasomes or RIP3. Hence, Fas controls a novel noncanonical IL-1beta activation pathway in myeloid cells, which could play an essential role in inflammatory processes, tumor surveillance, and control of infectious diseases. |
