Internalization, axonal transport and release of fibrillar forms of alpha-synuclein

NEUROBIOLOGY OF DISEASE

卷:109

Review

Bieri, Gregor^1,2  Gitler, Aaron D.¹  Brahic, Michel¹ 

[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA

[2] Stanford Univ, Sch Med, Neurosci Grad Program, Stanford, CA 94305 USA

关键词: Alpha-synuclein;    Axonal transport;    Exosome;    Fibrils;    Parkinson's disease;    Prion;    Spread;    Tunneling nanotube;    Unconventional secretion;   

DOI  :  10.1016/j.nbd.2017.03.007

来源: Elsevier

【 摘 要 】

Intra-neuronal protein aggregates made of fibrillar alpha-synuclein (alpha-syn) are the hallmark of Parkinson's disease (PD). With time, these aggregates spread through the brain following axonal projections. Understanding the mechanism of this spread is central to the study of the progressive nature of PD. Here we review data relevant to the uptake, transport and release of alpha-syn fibrils. We summarize several cell surface receptors that regulate the uptake of alpha-syn fibrils by neurons. The aggregates are then transported along axons, both in the anterograde and retrograde direction. The kinetics of transport suggests that they are part of the slow component b of axonal transport. Recent findings indicate that aggregated alpha-syn is secreted by neurons by non-canonical pathways that may implicate various molecular chaperones including USP19 and the DnaJ/Hsc70 complex. Additionally, alpha-syn fibrils may also be released and transmitted from neuron-to-neuron via exosomes and tunneling nano tubes. Understanding these different mechanisms and molecular players underlying alpha-syn spread is crucial for the development of therapies that could halt the progression of alpha-syn-related degenerative diseases. (C) 2017 The Authors. Published by Elsevier Inc.

【 授权许可】

Free