Kuznetsov I A, Kuznetsov A V
Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218-2694, USA; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Mechanical and Aerospace Engineering, North Carolina State University, Raleigh, NC 27695-7910, USA.
Math Biosci. 2016 Aug;278:22-9. doi: 10.1016/j.mbs.2016.05.002. Epub 2016 May 17.
The aim of this paper is to develop a minimal model describing events leading to the onset of Parkinson's disease (PD). The model accounts for α-synuclein (α-syn) production in the soma, transport toward the synapse, misfolding, and aggregation. The production and aggregation of polymeric α-syn is simulated using a minimalistic 2-step Finke-Watzky model. We utilized the developed model to analyze what changes in a healthy neuron are likely to lead to the onset of α-syn aggregation. We checked the effects of interruption of α-syn transport toward the synapse, entry of misfolded (infectious) α-syn into the somatic and synaptic compartments, increasing the rate of α-syn synthesis in the soma, and failure of α-syn degradation machinery. Our model suggests that failure of α-syn degradation machinery is probably the most likely cause for the onset of α-syn aggregation leading to PD.
本文的目的是建立一个描述导致帕金森病(PD)发病过程的最小模型。该模型考虑了α-突触核蛋白(α-syn)在胞体中的产生、向突触的运输、错误折叠和聚集。使用简约的两步Finke-Watzky模型模拟聚合α-syn的产生和聚集。我们利用所开发的模型分析健康神经元中的哪些变化可能导致α-syn聚集的发生。我们检查了α-syn向突触运输中断、错误折叠(有传染性)的α-syn进入胞体和突触区室、胞体中α-syn合成速率增加以及α-syn降解机制失效的影响。我们的模型表明,α-syn降解机制失效可能是导致α-syn聚集进而引发PD的最可能原因。