Kurowska Zuzanna, Kordower Jeffrey H, Stoessl A Jon, Burke Robert E, Brundin Patrik, Yue Zhenyu, Brady Scott T, Milbrandt Jeffrey, Trapp Bruce D, Sherer Todd B, Medicetty Satish
Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
Renovo Neural Inc., Cleveland, OH, USA.
J Parkinsons Dis. 2016 Oct 19;6(4):703-707. doi: 10.3233/JPD-160881.
Recent research suggests that in Parkinson's disease the long, thin and unmyelinated axons of dopaminergic neurons degenerate early in the disease process. We organized a workshop entitled 'Axonal Pathology in Parkinson's disease', on March 23rd, 2016, in Cleveland, Ohio with the goals of summarizing the state-of-the-art and defining key gaps in knowledge. A group of eight research leaders discussed new developments in clinical pathology, functional imaging, animal models, and mechanisms of degeneration including neuroinflammation, autophagy and axonal transport deficits. While the workshop focused on PD, comparisons were made to other neurological conditions where axonal degeneration is well recognized.
最近的研究表明,在帕金森病中,多巴胺能神经元长而细且无髓鞘的轴突在疾病进程早期就会发生退化。2016年3月23日,我们在俄亥俄州克利夫兰组织了一次题为“帕金森病中的轴突病理学”的研讨会,目的是总结最新技术水平并确定知识方面的关键差距。八位研究带头人组成的小组讨论了临床病理学、功能成像、动物模型以及包括神经炎症、自噬和轴突运输缺陷在内的退化机制方面的新进展。虽然研讨会聚焦于帕金森病,但也与其他已充分认识到轴突退化的神经疾病进行了比较。