The PINK1/Parkin pathway, a complex route to Parkinson’s disease

old_uid16697
titleThe PINK1/Parkin pathway, a complex route to Parkinson’s disease
start_date2018/11/09
schedule11h
onlineno
location_infoSalle Conférence IBCG
detailsséminaire axe neuro
summaryMitochondrial dysfunction has long been suspected to play a role in the pathogenesis of Parkinson’s disease. This hypothesis has received strong support in recent years, with the discovery of gene responsible for familial Parkinson’s disease playing roles in mitochondrial maintenance. The products of the PINK1 and PARK2 (Parkin) genes cooperate in sensing mitochondrial dysfunction and linking it to the activation of protective mitochondrial quality control programs, including mitophagy. Despite the remarkable advances in our understanding of the molecular mechanisms by which PINK1 and Parkin promote mitophagy, little is known about how their dysfunction leads to neuronal degeneration. I will present recent efforts from our laboratory to understand how dysfunction of the PINK1/Parkin pathway impact impairs the ability of neurons to respond to mitochondrial stress, focusing on both cell autonomous and non-autonomous mechanisms. I will also present a new mechanism by which PINK1 and Parkin preserve the quality of mitochondria.
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