Alpha Synuclein: Neurodegeneration and Inflammation

Alpha-Synuclein (a-Syn) is one of the most important molecules involved in the pathogenesis of Parkinson's disease and related disorders, synucleinopathies, but also in several other neurodegenerative disorders with a more elusive role. This review analyzes the activities of a-Syn, in different conformational states, monomeric, oligomeric and fibrils, in relation to neuronal dysfunction. The neuronal damage induced by a-Syn in various conformers will be analyzed in relation to its capacity to spread the intracellular aggregation seeds with a prion-like mechanism. In view of the prominent role of inflammation in virtually all neurodegenerative disorders, the activity of a-Syn will also be illustrated considering its influence on glial reactivity. We and others have described the interaction between general inflammation and cerebral dysfunctional activity of a-Syn. Differences in microglia and astrocyte activation have also been observed when in vivo the presence of a-Syn oligomers has been combined with a lasting peripheral inflammatory effect. The reactivity of microglia was amplified, while astrocytes were damaged by the double stimulus, opening new perspectives for the control of inflammation in synucleinopathies. Starting from our studies in experimental models, we extended the perspective to find useful pointers to orient future research and potential therapeutic strategies in neurodegenerative disorders.

Automated summary

This review discusses the important role of Alpha-Synuclein (a-Syn) in the pathogenesis of Parkinson's disease and related disorders. It analyzes the activities of a-Syn in different states, including monomeric, oligomeric, and fibrils, and their relation to neuronal dysfunction. The review also considers the influence of a-Syn on glial reactivity and the interaction between general inflammation and a-Syn activity. The findings provide insights into potential therapeutic strategies for neurodegenerative disorders.