Matsumoto A
Department of Radiation Biophysics and Genetics, Kobe University School of Medicine, Japan.
Biochim Biophys Acta. 1994 Feb 22;1225(3):304-10. doi: 10.1016/0925-4439(94)90011-6.
By pulse-chase analysis of cytosol and extracellular proteins, lymphoblastoid cells derived from patients with early- and late-onset familial Alzheimer's disease exhibit delayed and deficient processing characteristics of beta-amyloid precursor protein and its fragments. During 120 min chase incubation, 70-80% of the 16-kDa fragment with beta/A4-amyloid and cytoplasmic domains is removed in both cytosol and serum-free media of normal cells, whereas it remained unprocessed or even accumulated in familial Alzheimer's disease cells. Two-dimensional gel analysis further clarified that the 16-kDa peptide in familial Alzheimer's disease cells is highly phosphorylated compared with normals, and almost all of the accumulated 16-kDa preamyloid after 60 min chase incubation is phosphorylated in these cells. Tris-tricine gel analysis revealed a difference of processing characteristics between cytosol and extracellular beta/A4-containing peptides. Cytosol APP as the 16-kDa band in Tris-glycine gel was further separated into five peptides with molecular mass of 11 kDa-16.5 kDa, and some early-onset familial Alzheimer's disease cells contain 3-6 kDa peptides with beta/A4 domain, that are generated by proteolysis around transmembrane domain. Extracellular APP secreted during 24 h serum-free culture, however, exhibits only beta/A4-cytoplasmic domain-containing peptides with 12 kDa band as major component, but no 3-6 kDa peptides both in normal and familial Alzheimer's disease cells. These findings suggest that familial Alzheimer's disease lymphoblastoid cells harbour biochemical abnormality in the APP processing step to generate beta/A4-cytoplasmic domain peptides, and intracellular processing is crucial for eventual accumulation of beta/A4-amyloid in lymphoblastoid cells.
通过对胞质溶胶和细胞外蛋白质进行脉冲追踪分析,早发性和晚发性家族性阿尔茨海默病患者来源的淋巴母细胞样细胞表现出β-淀粉样前体蛋白及其片段的加工延迟和缺陷特征。在120分钟的追踪孵育过程中,正常细胞的胞质溶胶和无血清培养基中,70%-80%带有β/A4淀粉样蛋白和细胞质结构域的16 kDa片段被去除,而在家族性阿尔茨海默病细胞中,该片段未被加工甚至积累。二维凝胶分析进一步表明,与正常细胞相比,家族性阿尔茨海默病细胞中的16 kDa肽高度磷酸化,在追踪孵育60分钟后,这些细胞中几乎所有积累的16 kDa淀粉样前体蛋白都被磷酸化。Tris-三羟甲基氨基甲烷凝胶分析揭示了胞质溶胶和细胞外含β/A4肽的加工特征存在差异。Tris-甘氨酸凝胶中作为16 kDa条带的胞质溶胶APP进一步分离为5种分子量在11 kDa-16.5 kDa之间的肽,一些早发性家族性阿尔茨海默病细胞含有带有β/A4结构域的3 kDa-6 kDa肽,这些肽是由跨膜结构域周围的蛋白水解产生的。然而,在无血清培养24小时期间分泌的细胞外APP,在正常细胞和家族性阿尔茨海默病细胞中均仅以12 kDa条带的含β/A4-细胞质结构域的肽为主要成分,没有3 kDa-6 kDa的肽。这些发现表明,家族性阿尔茨海默病淋巴母细胞样细胞在APP加工步骤中存在生化异常,以产生β/A4-细胞质结构域肽,并且细胞内加工对于淋巴母细胞样细胞中β/A4淀粉样蛋白的最终积累至关重要。