Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

被引:4861
作者
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. [1 ]
机构
[1] Univ Penn, Sch Med, Ctr Neurodegenerat Dis Res, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Neurol, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Alzheimers Dis Core Ctr, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Med, Inst Aging, Philadelphia, PA 19104 USA
[6] Univ San Francisco, Dept Neurol, San Francisco, CA 94117 USA
[7] Univ Calif San Diego, Sch Med, Dept Neurosci, La Jolla, CA 92093 USA
[8] Univ British Columbia, Dept Pathol, Vancouver, BC V6T 2B5, Canada
[9] Univ British Columbia, Div Neurol, Vancouver, BC V6T 2B5, Canada
[10] Univ Saarland, Inst Neuropathol, D-66421 Homburg, Germany
[11] Univ Munich, Ctr Neuropathol & Prion Res, D-81377 Munich, Germany
关键词
D O I
10.1126/science.1134108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 hyperphosphorylated, 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.
引用
收藏
页码:130 / 133
页数:4
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