contribute to Aβ propagation into unaffected brain regions remains unknown. Using
transplantation of wild-type (WT) neurons, we show that Aβ enters WT grafts, and that this is
accompanied by microglia infiltration. Manipulation of microglia function reduced Aβ
deposition within grafts. Furthermore, in vivo imaging identified microglia as carriers of Aβ
pathology in previously unaffected tissue. Our data thus argue for a hitherto unexplored …