Laboratory for Neurobiology, Experimental Neurology, K.U.Leuven, Herestraat, 3000 Leuven, Belgium.
Eur J Neurosci. 2010 Jun;31(12):2247-65. doi: 10.1111/j.1460-9568.2010.07260.x. Epub 2010 Jun 7.
Amyotrophic lateral sclerosis is a degenerative disease affecting the motor neurons. In spite of our growing insights into its biology, it remains a lethal condition. The identification of the cause of several of the familial forms of ALS allowed generation of models to study this disease both in vitro and in vivo. Here, we summarize what is known about the pathogenic mechanisms of ALS induced by hereditary mutations, and attempt to identify the relevance of these findings for understanding the pathogenic mechanisms of the sporadic form of this disease.
肌萎缩侧索硬化症是一种影响运动神经元的退行性疾病。尽管我们对其生物学的认识不断加深,但它仍然是一种致命的疾病。几种家族性肌萎缩侧索硬化症的病因的确定,使得人们能够生成模型来在体外和体内研究这种疾病。在这里,我们总结了遗传性突变引起的肌萎缩侧索硬化症的发病机制,并试图确定这些发现对理解这种疾病散发性形式的发病机制的相关性。