Spatiotemporal analysis of axonal autophagosome-lysosome dynamics reveals limited fusion events trigger two-step maturation

Abstract

Macroautophagy is a homeostatic process required to clear cellular waste including aggregated proteins and dysfunctional organelles. Neuronal autophagosomes form constitutively in the distal tip of the axon and are actively transported toward the soma, with cargo degradation initiated en route. Cargo turnover requires autophagosomes to fuse with lysosomes to acquire degradative enzymes; however, the timing and number of these fusion events in the axon have proven difficult to detect using microscopy alone. Here we use a quantitative model, parameterized and validated using data from live and fixed imaging of primary hippocampal neurons, to explore the autophagosome maturation process on a cellular scale. We demonstrate that retrograde autophagosome motility is independent from lysosomal fusion, and that most autophagosomes fuse with only a few lysosomes by the time they reach the soma. Furthermore, our imaging and model results highlight the two-step maturation of the autophagosome: fusion with a lysosome or late endosome is followed by the slow degradation of the autophagosomal inner membrane before actual cargo degradation can occur. Together, rigorous quantitative measurements and mathematical modeling elucidate the dynamics of autophagosome-lysosome interaction and autophagosomal maturation in the axon.