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巴顿病及无关溶酶体疾病中线粒体ATP合酶亚基c(SCMAS)的随访研究

Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disorders.

作者信息

Elleder M, Sokolová J, Hrebícek M

机构信息

Center of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Praha, Czech Republic.

出版信息

Acta Neuropathol. 1997 Apr;93(4):379-90. doi: 10.1007/s004010050629.

Abstract

Immunohistochemical and biochemical studies of subunit c of mitochondrial ATP synthase (SCMAS) storage were carried out in neuronal ceroid lipofuscinosis (NCL) and in a series of unrelated inherited and acquired lysosomal disorders. In the NCL group, represented by the late infantile, early juvenile and juvenile types, SCMAS storage was generalized neurovisceral, with considerable difference in the visceral storage pattern between the types. In late infantile NCL the SCMAS storage was intensive and corresponded to the generalized, autofluorescent, uniformly curvilinear material, irrespective of the cell type affected. In both early juvenile and juvenile NCLs the SCMAS storage was strong and almost uniform in brain neurons, but did not correlate entirely with the visceral autofluorescent storage pool, being undetectable in autofluorescent storage deposits in a constant set of tissues. In the adult (Kufs) type, the brain neurons were stained with various intensity. In infantile NCL, SCMAS storage was restricted to some of the persisting neurons. In a series of inherited lysosomal enzymopathies and acquired lysosomal disorders, excessive SCMAS accumulation was found only in secondary neuronal lipopigments. It occurred as an early and more uniform phenomenon in mucopolysaccharidosis types I, II, IIIA and in polysulphatase deficiency, or as a delayed varied phenomenon in protracted variants of mucolipidosis I, Niemann-Pick types A and C, and GM2 and GM1 gangliosidoses. Neuronal ageing led to an irregular increase in immunodetectable SCMAS epitope in some neuronal lipofuscin granules. There was no evidence of significant SCMAS lysosomal accumulation in non-neural cells in the whole group, regardless of whether lipofuscin or ceroid accumulation occurred or not. The neuronal SCMAS storage is thus nosologically a common unspecific phenomenon, which is especially amplified in NCL. The specificity of the NCL storage process is shown by the fact that even lysosomes of non-neuronal cells in NCL accumulate SCMAS.

摘要

对线粒体ATP合酶亚基c(SCMAS)储存进行了免疫组织化学和生化研究,研究对象为神经元蜡样脂褐质沉积症(NCL)以及一系列不相关的遗传性和获得性溶酶体疾病。在以晚婴儿型、早青少年型和青少年型为代表的NCL组中,SCMAS储存呈全身性神经内脏性,各类型之间内脏储存模式存在显著差异。在晚婴儿型NCL中,SCMAS储存强烈,对应于全身性、自发荧光、均匀曲线状物质,与受影响的细胞类型无关。在早青少年型和青少年型NCL中,SCMAS储存在脑神经元中均较强且几乎均匀,但与内脏自发荧光储存池并不完全相关,在一组恒定组织的自发荧光储存沉积物中无法检测到。在成人(Kufs)型中,脑神经元染色强度各异。在婴儿型NCL中,SCMAS储存仅限于一些残留的神经元。在一系列遗传性溶酶体酶病和获得性溶酶体疾病中,仅在继发性神经元脂褐素中发现SCMAS过度积累。它在I型、II型、IIIA型黏多糖贮积症和多硫酸酯酶缺乏症中作为早期且更均匀的现象出现,或在I型黏脂贮积症、尼曼-匹克病A和C型以及GM2和GM1神经节苷脂病的迁延型中作为延迟的多样现象出现。神经元衰老导致一些神经元脂褐质颗粒中免疫可检测的SCMAS表位不规则增加。在整个组的非神经细胞中,无论是否发生脂褐素或类蜡质积累,均无明显的SCMAS溶酶体积累证据。因此,神经元SCMAS储存从病因学角度来看是一种常见的非特异性现象,在NCL中尤其明显。NCL储存过程的特异性表现为,即使是NCL中非神经细胞的溶酶体也会积累SCMAS。

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