Inclusion formation and neuronal cell death through neuron-to-neuron transmission of α-synuclein

P Desplats, HJ Lee, EJ Bae, C Patrick… - Proceedings of the …, 2009 - National Acad Sciences
P Desplats, HJ Lee, EJ Bae, C Patrick, E Rockenstein, L Crews, B Spencer, E Masliah…
Proceedings of the National Academy of Sciences, 2009National Acad Sciences
Neuronal accumulation of α-synuclein and Lewy body formation are characteristic to many
neurodegenerative diseases, including Parkinson's disease (PD). This Lewy pathology
appears to spread throughout the brain as the disease progresses. Furthermore, recent
studies showed the occurrence of Lewy pathology in neurons grafted into the brains of PD
patients, suggesting the spread of pathology from the host tissues to the grafts. The
mechanism underlying this propagation is unknown. Here, we show that α-synuclein is …
Neuronal accumulation of α-synuclein and Lewy body formation are characteristic to many neurodegenerative diseases, including Parkinson's disease (PD). This Lewy pathology appears to spread throughout the brain as the disease progresses. Furthermore, recent studies showed the occurrence of Lewy pathology in neurons grafted into the brains of PD patients, suggesting the spread of pathology from the host tissues to the grafts. The mechanism underlying this propagation is unknown. Here, we show that α-synuclein is transmitted via endocytosis to neighboring neurons and neuronal precursor cells, forming Lewy-like inclusions. Moreover, α-synuclein was transmitted from the affected neurons to engrafted neuronal precursor cells in a transgenic model of PD-like pathology. Failure of the protein quality control systems, especially lysosomes, promoted the accumulation of transmitted α-synuclein and inclusion formation. Cells exposed to neuron-derived α-synuclein showed signs of apoptosis, such as nuclear fragmentation and caspase 3 activation, both in vitro and in vivo. These findings demonstrate the cell-to-cell transmission of α-synuclein aggregates and provide critical insights into the mechanism of pathological progression in PD and other proteinopathies.
National Acad Sciences