Neumann Manuela, Sampathu Deepak M, Kwong Linda K, Truax Adam C, Micsenyi Matthew C, Chou Thomas T, Bruce Jennifer, Schuck Theresa, Grossman Murray, Clark Christopher M, McCluskey Leo F, Miller Bruce L, Masliah Eliezer, Mackenzie Ian R, Feldman Howard, Feiden Wolfgang, Kretzschmar Hans A, Trojanowski John Q, Lee Virginia M-Y
Center for Neurodegenerative Disease Research, Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Science. 2006 Oct 6;314(5796):130-3. doi: 10.1126/science.1134108.
Ubiquitin-positive, tau- and alpha-synuclein-negative inclusions are hallmarks of frontotemporal lobar degeneration with ubiquitin-positive inclusions and amyotrophic lateral sclerosis. Although the identity of the ubiquitinated protein specific to either disorder was unknown, we showed that TDP-43 is the major disease protein in both disorders. Pathologic TDP-43 was hyper-phosphorylated, ubiquitinated, and cleaved to generate C-terminal fragments and was recovered only from affected central nervous system regions, including hippocampus, neocortex, and spinal cord. TDP-43 represents the common pathologic substrate linking these neurodegenerative disorders.
泛素阳性、tau蛋白和α-突触核蛋白阴性的包涵体是伴有泛素阳性包涵体的额颞叶痴呆和肌萎缩侧索硬化的标志。尽管这两种疾病中特异性泛素化蛋白的身份尚不清楚,但我们发现TDP-43是这两种疾病中的主要致病蛋白。病理性TDP-43发生了过度磷酸化、泛素化,并被切割产生C端片段,且仅在包括海马体、新皮质和脊髓在内的受影响中枢神经系统区域中检测到。TDP-43代表了连接这些神经退行性疾病的常见病理底物。