characterized by photoreceptor and retinal pigment epithelium (RPE) atrophy. In these
blinding diseases, macrophages accumulate at atrophic sites, but their ontogeny and niche
specialization remain poorly understood, especially in humans. We uncovered a unique
profile of microglia, marked by galectin-3 upregulation, at atrophic sites in mouse models of
retinal degeneration and human AMD. In disease models, conditional deletion of galectin-3 …