TLR7/8 stress response drives histiocytosis in SLC29A3 disorders

This is the authors' abstract. We don't add key points for this paper.

SLC29A3, also known as ENT3, is a lysosomal transmembrane protein that transports nucleosides from the lysosomes to the cytoplasm 1 . Loss-of-function mutations in SLC29A3 cause lysosomal nucleoside storage and histiocytosis: phagocyte accumulation in multiple organs 2,3 . However, little is known about the mechanism through which lysosomal nucleoside storage drives histiocytosis. Herein, histiocytosis in Slc29a3 −/− mice was demonstrated to depend on TLR7, which senses a combination of nucleosides and oligoribonucleotides 4,5 . TLR7 responded to lysosomal nucleoside storage and enhanced proliferation of Ly6C hi CX3CR1 low immature monocytes and their maturation into Ly6C low phagocytes in Slc29a3 −/− mice. Because accumulated nucleosides primarily originated from cell corpse phagocytosis, TLR7 in immature monocytes recognized nucleoside storage as lysosomal stress and increased phagocyte numbers. This non-inflammatory compensatory response is referred to as the TLR7 stress response where Syk, GSK3β, β-catenin, and mTORC1 serve as downstream signalling molecules. In SLC29A3 disorders, histiocytosis accompanies inflammation 6,7 . Nucleoside storage failed to induce pro-inflammatory cytokine production in Slc29a3 −/− mice, but enhanced ssRNA-dependent pro-inflammatory cytokine production in Ly6C hi classical monocytes and peripheral macrophages, not proliferating immature monocytes. Patient-derived monocytes harbouring G208R SLC29A3 mutation showed higher survival and proliferation in the presence of M-CSF and produced larger amounts of IL-6 upon ssRNA stimulation than did those derived from healthy subjects. A TLR8 antagonist inhibited the survival/proliferation of patient-derived macrophages. These results demonstrated that TLR7/8 responses to lysosomal nucleoside stress drive SLC29A3 disorders.