自噬
α-突触核蛋白
帕金森病
微泡
分泌物
外体
多巴胺能
疾病
溶酶体
生物标志物
细胞生物学
生物
神经科学
医学
病理
内分泌学
多巴胺
小RNA
生物化学
基因
细胞凋亡
酶
作者
Denisse Sepúlveda,Marisol Cisternas-Olmedo,Javiera Arcos,Melissa Nassif,René L. Vidal
标识
DOI:10.3389/fnmol.2022.805087
摘要
Parkinson’s disease (PD) is caused by the degeneration of dopaminergic neurons due to an accumulation of intraneuronal abnormal alpha-synuclein (α-syn) protein aggregates. It has been reported that the levels of exosomal α-syn of neuronal origin in plasma correlate significantly with motor dysfunction, highlighting the exosomes containing α-syn as a potential biomarker of PD. In addition, it has been found that the selective autophagy-lysosomal pathway (ALP) contributes to the secretion of misfolded proteins involved in neurodegenerative diseases. In this review, we describe the evidence that supports the relationship between the ALP and α-syn exosomal secretion on the PD progression and its implications in the diagnosis and progression of this pathology.
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