Mutations in LRRK2 potentiate age-related impairment of autophagic flux

作者：Saha Shamol; Ash Peter E A; Gowda Vivek; Liu Liqun; Shirihai Orian; Wolozin Benjamin^*

来源：Molecular Neurodegeneration, 2015, 10(1): 26.

DOI：10.1186/s13024-015-0022-y

• C. elegans
• Autophagy
• LRRK2
• alpha-synuclein
• Imaging
• LC3
• Aging

Autophagy is thought to play a pivotal role in the pathophysiology of Parkinson's disease, but little is known about how genes linked to PD affect autophagy in the context of aging. We generated lines of C. elegans expressing reporters for the autophagosome and lysosome expressed only in dopaminergic neurons, and examined autophagy throughout the lifespan in nematode lines expressing LRRK2 and alpha-synuclein. Dopamine neurons exhibit a progressive loss of autophagic function with aging. G2019S LRRK2 inhibited autophagy and accelerated the age-related loss of autophagic function, while WT LRRK2 improved autophagy throughout the life-span. Expressing alpha-synuclein with G2019S or WT LRRK2 caused age-related synergistic inhibition of autophagy and increase in degeneration of dopaminergic neurons. The presence of alpha-synuclein particularly accentuated age-related inhibition of autophagy by G2019S LRRK2. This work indicates that LRRK2 exhibits a selective, age-linked deleterious interaction with alpha-synuclein that promotes neurodegeneration.

• 出版日期2015-7-11