| First Author | Babdor J | Year | 2017 |
| Journal | Nat Immunol | Volume | 18 |
| Issue | 5 | Pages | 509-518 |
| PubMed ID | 28319098 | Mgi Jnum | J:260126 |
| Mgi Id | MGI:6140999 | Doi | 10.1038/ni.3711 |
| Citation | Babdor J, et al. (2017) IRAP(+) endosomes restrict TLR9 activation and signaling. Nat Immunol 18(5):509-518 |
| abstractText | The retention of intracellular Toll-like receptors (TLRs) in the endoplasmic reticulum prevents their activation under basal conditions. TLR9 is activated by sensing ligands in specific endosomal-lysosomal compartments. Here we identified IRAP(+) endosomes as major cellular compartments for the early steps of TLR9 activation in dendritic cells (DCs). Both TLR9 and its ligand, the dinucleotide CpG, were present as cargo in IRAP(+) endosomes. In the absence of the aminopeptidase IRAP, the trafficking of CpG and TLR9 to lysosomes and signaling via TLR9 were enhanced in DCs and in mice following bacterial infection. IRAP stabilized CpG-containing endosomes by interacting with the actin-nucleation factor FHOD4, which slowed the trafficking of TLR9 toward lysosomes. Thus, endosomal retention of TLR9 via the interaction of IRAP with the actin cytoskeleton is a mechanism that prevents hyper-activation of TLR9 in DCs. |
