Decreased lysosomal subunit c-degrading activity in fibroblasts from patients with late infantile neuronal ceroid lipofuscinosis

被引:7
作者
Ezaki, J
Wolfe, LS
Kominami, E
机构
[1] JUNTENDO UNIV,SCH MED,DEPT BIOCHEM,BUNKYO KU,TOKYO 113,JAPAN
[2] MCGILL UNIV,MONTREAL NEUROL INST,MONTREAL,PQ H3A 2B4,CANADA
关键词
subunit c; Batten disease; proteolysis;
D O I
10.1055/s-2007-973668
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We investigated in in-vitro cell-free incubation experiments which factor, lysosomal proteolytic dysfunction or structural alteration of subunit c, is responsible for the specific delay in the degradation of subunit c in patient cells with the late infantile form of neuronal ceroid lipofuscinosis. Experiments using substrates and soluble lysosomal fractions isolated separately from control and patient cells indicated that lysosomes from control cells are able to degrade mitochondrial subunit c either from control or patient cells at much faster rate than lysosomes from patient cells. Subunit c stored in patient cell lysosomes showed much more resistance to proteolytic attack than mitochondrial subunit c, suggesting that conformation of subunit c as well as lysosomal proteolytic dysfunction both participate in the specific lysosomal accumulation of subunit c in the late infantile disease.
引用
收藏
页码:53 / 55
页数:3
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