神经突
共核细胞病
纤维
神经元
路易体
神经科学
α-突触核蛋白
细胞生物学
路易氏体型失智症
生物
化学
生物物理学
帕金森病
病理
生物化学
医学
体外
疾病
痴呆
作者
Laura A. Volpicelli‐Daley,Kelvin C. Luk,Virginia M.‐Y. Lee
出处
期刊:Nature Protocols
[Springer Nature]
日期:2014-08-14
卷期号:9 (9): 2135-2146
被引量:570
标识
DOI:10.1038/nprot.2014.143
摘要
Lewy bodies and Lewy neurites are found in the brains of patients with Parkinson's disease and other synucleinopathies. This protocol describes how to model this by inducing α-synuclein aggregates in a primary neuronal culture system. This protocol describes a primary neuronal model of formation of α-synuclein (α-syn) aggregates that recapitulate features of the Lewy bodies and Lewy neurites found in Parkinson's disease brains and other synucleinopathies. This model allows investigation of aggregate formation, their impact on neuron function, and development of therapeutics. Addition of preformed fibrils (PFFs) synthesized from recombinant α-syn to neurons seeds the recruitment of endogenous α-syn into aggregates characterized by detergent insolubility and hyperphosphorylation. Aggregate formation follows a lag phase of 2–3 d, followed by formation in axons by days 4–7, spread to somatodendritic compartments by days 7–10 and neuron death ∼14 d after PFF addition. Here we provide methods and highlight the crucial steps for PFF formation, PFF addition to cultured hippocampal neurons and confirmation of aggregate formation. Neurons derived from various brain regions from nontransgenic and genetically engineered mice and rats can be used, allowing interrogation of the effect of specific genes on aggregate formation.
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