Open AccessThe deletion of the C‐terminal tail and addition of an endoplasmic reticulum targeting signal to Alzheimer's amyloid precursor protein change its localization, secretion, and intracellular proteolysis
Author(s) -
Kouchi Zen,
Kinouchi Tadatoshi,
Sorimachi Hiroyuki,
Ishiura Shoichi,
Suzuki Koichi
Publication year - 1998
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1046/j.1432-1327.1998.2580291.x
Subject(s) - endoplasmic reticulum , secretion , amyloid precursor protein , intracellular , proteolysis , microbiology and biotechnology , secretory pathway , signal peptide , biochemistry , golgi apparatus , er retention , immunoprecipitation , biology , secretory protein , amyloid precursor protein secretase , internalization , p3 peptide , chemistry , peptide sequence , cell , alzheimer's disease , enzyme , medicine , mutant , disease , gene
The metabolic pathway of Alzheimer's amyloid precursor protein (APP) involves restricted intracellular proteolysis by secretases, which leads to the secretion of the N‐terminal soluble APP (sAPP) and the generation of a cell‐associated C‐terminal fragment. The precise cellular sites at which these processes occur remain unknown. In this report, we describe the route of APP sorting and the processing site using novel systems with and without sorting signals on the APP molecule. One system involves the replacement of the C‐terminal ten amino acids of APP with Adenoviral E19 protein containing an endoplasmic reticulum (ER) retrieval signal (APPE19); the other involves deleting the last ten amino acids correponding to the replaced site (APPdeltaC10). APPE19 localized mainly within the cis/medial Golgi compartment and exclusively suppresses the secretion of APP. In contrast, deletion of the C‐terminal tail promotes sAPP secretion by a constitutive secretion pathway. Metabolic labeling followed by immunoprecipitation with anti‐APP antibody revealed that APPE19 is rapidly degraded within 30 min and that the subsequent intracellular turnover rate is decreased with 40 % of the protein retained within the cells even after a chase period a 3 h. In contrast, APPdeltaC10 is rapidly eliminated from the intracellular compartments and secreted into the culture medium. The surface internalization and recycling processes of this protein are relatively impaired compared with wild‐type APP. The ratios of the levels of production to secretion of sAPPα, the N‐terminal, soluble APP fragment released by α‐secretase, are proportional to the secretion efficiencies among APP species, suggesting the localization of α‐secretase within a compartment late in the constitutive secretion pathway. These secretion mutants which utilize ER targeting signals are useful tools for analyzing the location of secretases and the intracellular degradation system within a constitutive secretion pathway such as ER quality control.