Autophagy is a regulated lysosomal degradation process that involves autophagosome formation and transport. Although recent evidence indicates that basal levels of autophagy protect against neurodegeneration, the exact mechanism whereby this occurs is not known. By using conditional knockout mutant mice, we report that neuronal autophagy is particularly important for the maintenance of local homeostasis of axon terminals and protection against axonal degeneration. We show that specific ablation of an essential autophagy gene, Atg7, in Purkinje cells initially causes cell-autonomous, progressive dystrophy (manifested by axonal swellings) and degeneration of the axon terminals. Consistent with suppression of autophagy, no autophagosomes are observed in these dystrophic swellings, which is in contrast to accumulation of autophagosomes in the axonal dystrophic swellings under pathological conditions. Axonal dystrophy of mutant Purkinje cells proceeds with little sign of dendritic or spine atrophy, indicating that axon terminals are much more vulnerable to autophagy impairment than dendrites. This early pathological event in the axons is followed by cell-autonomous Purkinje cell death and mouse behavioral deficits. Furthermore, ultrastructural analyses of mutant Purkinje cells reveal an accumulation of aberrant membrane structures in the axonal dystrophic swellings. Finally, we observe double-membrane vacuole-like structures in wild-type Purkinje cell axons, whereas these structures are abolished in mutant Purkinje cell axons. Thus, we conclude that the autophagy protein Atg7 is required for membrane trafficking and turnover in the axons. Our study implicates impairment of axonal autophagy as a possible mechanism for axonopathy associated with neurodegeneration.axon ͉ axonopathy ͉ neurodegeneration ͉ autophagosome ͉ Purkinje cell M acroautophagy is characterized by dynamic membrane rearrangements, involving the formation, trafficking, and degradation of double-membrane autophagic vacuoles (autophagosomes) in the cytoplasm. Macroautophagy (hereafter referred to as autophagy) is a highly regulated process, which can be induced by nutrient starvation, trophic factors, and stress (1). Despite recent advances in characterizing autophagy in several model systems, autophagic processes in the nervous system remain poorly understood. On one hand, nutrient deprivation has not been observed to induce autophagy in the mammalian brain (2), thus suggesting a specific regulatory system for autophagy that is not typically activated by starvation. On the other hand, a variety of conditions that cause neuronal stress or degeneration can lead to the accumulation of autophagosomes in neurons, thus implicating autophagy in these neuropathogenic processes (3, 4).The axon is a highly specialized neuronal compartment that performs many functions independently from the cell body. After axotomy or excitotoxicity, double-membrane vacuoles resembling autophagosomes were originally observed to accumulate in dilated axon terminals that result fro...