Lysosomal dysfunction in Parkinson disease

Lysosomal enzyme defects and Parkinson disease.

Targeting the Autophagy/Lysosomal Degradation Pathway in Parkinson´s Disease

Autophagy is a cellular quality control mechanism crucial for neuronal homeostasis. Defects in autophagy are critically associated with mechanisms underlying Parkinson's disease (PD), a common and debilitating neurodegenerative disorder. Autophagic dysfunction in PD can occur at several stages of the autophagy/lysosomal degradative machinery, contributing to the formation of intracellular prote...

Lysosomal function and dysfunction: mechanism and disease.

SIGNIFICANCE Lysosomes are organelles in which cellular degradation occurs in a controlled manner, separated from other cellular components. As several pathways terminate in the lysosome, lysosomal dysfunction has a profound impact on cell homeostasis, resulting in manifold pathological situations, including infectious diseases, neurodegeneration, and aging. RECENT ADVANCES Lysosomal biology ...

Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts

Mutations in PARK2, encoding Parkin, cause an autosomal recessive form of juvenile Parkinson Disease (JPD). The aim of the present study was to investigate the impact of PARK2 mutations on mitochondrial function and morphology in human skin fibroblasts. We analyzed cells obtained from four patients clinically characterized by JPD, harboring recessive mutations in PARK2. By quantitative PCR we f...

olfactory dysfunction in persian patients suffering from parkinson's disease.

background: looking in literature reveals that aging is accompanied by olfactory dysfunction and hyposmia/anosmia is a common manifestation in some neurodegenerative disorders. olfactory dysfunction is regarded as non-motor manifestations of parkinson disease (pd). the main goal of this study was to examine the extent of olfactory dysfunction in persian pd patients. methods: we used seven types...