UBIQUITIN IN MOTOR-NEURON DISEASE - STUDY AT THE LIGHT AND ELECTRON-MICROSCOPE

被引:63
作者
SCHIFFER, D
AUTILIOGAMBETTI, L
CHIO, A
GAMBETTI, P
GIORDANA, MT
GULLOTTA, F
MIGHELI, A
VIGLIANI, MC
机构
[1] UNIV MUNSTER, INST NEUROPATHOL, W-4400 MUNSTER, GERMANY
[2] CASE WESTERN RESERVE UNIV, INST PATHOL, DIV NEUROPATHOL, CLEVELAND, OH 44106 USA
关键词
IMMUNOELECTRON MICROSCOPY; IMMUNOHISTOCHEMISTRY; MOTOR NEURON DISEASE; NEUROFILAMENTS; UBIQUITIN;
D O I
10.1097/00005072-199107000-00007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several neurodegenerative diseases, including motor neuron disease (MND), are characterized by formation of abnormal cytoskeleton-derived inclusions which contain ubiquitin (Ubq). We have studied the distribution of Ubq in 26 cases of MND with light and electron microscopic immunocytochemistry. Ubiquitin-positive inclusions were found in neurons of anterior horns in most cases of amyotrophic lateral sclerosis (ALS) but were not present in other forms of MND. Ubiquitin immunoreactivity was observed in 10-15 nm intraneuronal filaments, which were not stained by antibodies to neurofilaments, and on dense bodies of dystrophic neurites throughout the neuropil of anterior horns and pyramidal tracts. Data analysis showed a trend toward lower percentage of Ubq-positive neurons in cases with longer duration of illness or lower number of neurons. A high percentage of Ubq-positive inclusions occurred in cases with an aggressive clinical course, suggesting that ubiquitination takes place at early stages of the disease.
引用
收藏
页码:463 / 473
页数:11
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