It has been 200 years since Parkinson disease (PD) was described by Dr. Parkinson in 1817. The disease is the second most common neurodegenerative disease characterized by a progressive loss of dopaminergic neurons in the substantia nigra pars compacta. Although the pathogenesis of PD is still unknown, the research findings from scientists are conducive to understand the pathological mechanisms. It is well accepted that both genetic and environmental factors contribute to the onset of PD. In this review, we summarize the mutations of main seven genes (α-synuclein, LRRK2, PINK1, Parkin, DJ-1, VPS35 and GBA1) linked to PD, discuss the potential mechanisms for the loss of dopaminergic neurons (dopamine metabolism, mitochondrial dysfunction, endoplasmic reticulum stress, impaired autophagy, and deregulation of immunity) in PD, and expect the development direction for treatment of PD.
Cellular and Molecular Basis of Neurodegeneration in Parkinson Disease
Xiansi Zeng,Wenshuo Geng,Jinjing Jia,Lei Chen,Peng-Peng Zhang
Published 2018 in Frontiers in Aging Neuroscience
ABSTRACT
PUBLICATION RECORD
- Publication year
2018
- Venue
Frontiers in Aging Neuroscience
- Publication date
2018-04-17
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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