期刊论文详细信息
FEBS Letters
The amyloid precursor protein of Alzheimer disease is expressed as a 130 kDa polypeptide in various cultured cell types
Schaetzle, B.1  Greenberg, B.2  Morandi, A.1  Gambetti, P.1  Perry, G.1  Kovacs, D.1  Autilio-Gambetti, L.1  Tabaton, M.1 
[1] Division of Neuropathology, Institute of Pathology, Case Western Reserve University, Cleveland, OH 44106 USA;The UpJohn Company, 301 Henrietta Street, Kalamazoo, MI 49001, USA
关键词: Amyloid;    Amyloid precursor protein;    Alzheimer's disease;    (Cell culture);   
DOI  :  10.1016/0014-5793(88)81038-X
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
PDF
【 摘 要 】

The vascular and parenchymal amyloid deposits in Alzheimer disease (AD), normal aging and Down syndrome are mainly composed of a 4 kDa polypeptide (A4), which derives from a larger precursor protein (APP). There is evidence that APP is a transmembrane glycoprotein present in most tissues, but the characteristics of APP in intact cells are not yet known. In order to investigate this issue, we examined the immunoreactivity of fibroblasts of human and nonhuman cell lines with antisera raised to synthetic peptides corresponding to A4 and to two other domains of the APP. All three antisera recognized a 130 kDa polypeptide (APP-130) in immunoblots from all cell lines. In fibroblasts, an additional polypeptide of 228 kDa (APP-228) was recognized by the antiserum to A4. In immunoblots of two dimensional gels, APP-130 showed a pI of 6.2, while APP-228 failed to focus in the pH range of 4.7–7.0. Sequential extractions of cells with buffer and with Triton X-100 indicate that APP-130 is extractable with nonionic detergents at high ionic strength, whereas 228 kDa APP is a cystolic component. Immunofluorescence staining is consistent with an intracellular perinuclear and plasma membrane localization. It is concluded that APP-130 and APP-228 are two forms of the APP which result from extensive posttranslational modifications of a smaller original gene product. It is likely that APP undergoes similar posttranslational modifications in different cell types.

【 授权许可】

Unknown   

【 预 览 】
附件列表
Files Size Format View
RO201912020291354ZK.pdf 426KB PDF download
  文献评价指标  
  下载次数:9次 浏览次数:9次