Intercellular transmission of alpha-synuclein

被引:2
|
作者
Wu, Shenjie [1 ]
Schekman, Randy W. [1 ]
机构
[1] Univ Calif Berkeley, Howard Hughes Med Inst, Dept Mol & Cell Biol, Berkeley, CA 94707 USA
来源
FRONTIERS IN MOLECULAR NEUROSCIENCE | 2024年 / 17卷
关键词
alpha synuclein; Parkinson's disease; Braak hypothesis; unconventional secretion; receptor-mediated uptake; endosome escape; tunneling nanotube; extracellular vesicle (EV); HEPARAN-SULFATE PROTEOGLYCAN; TO-NEURON TRANSMISSION; PARKINSONS-DISEASE; LEWY BODY; UNCONVENTIONAL SECRETION; FIBRILS; PATHOLOGY; TRANSLOCATION; BODIES; SPREAD;
D O I
10.3389/fnmol.2024.1470171
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
An emerging theme in Parkinson's disease (PD) is the propagation of alpha-synuclein pathology as the disease progresses. Research involving the injection of preformed alpha-synuclein fibrils (PFFs) in animal models has recapitulated the pathological spread observed in PD patients. At the cellular and molecular levels, this intercellular spread requires the translocation of alpha-synuclein across various membrane barriers. Recent studies have identified subcellular organelles and protein machineries that facilitate these processes. In this review, we discuss the proposed pathways for alpha-synuclein intercellular transmission, including unconventional secretion, receptor-mediated uptake, endosome escape and nanotube-mediated transfer. In addition, we advocate for a rigorous examination of the evidence for the localization of alpha-synuclein in extracellular vesicles.
引用
收藏
页数:12
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