INCREASED EXPRESSION OF AMYLOID PRECURSOR PROTEIN AND AMYLOID PRECURSOR-LIKE PROTEIN-2 DURING TROPHIC FACTOR WITHDRAWAL-INDUCED DEATH OF NEURONAL PC12 CELLS

Citation
W. Araki et Rj. Wurtman, INCREASED EXPRESSION OF AMYLOID PRECURSOR PROTEIN AND AMYLOID PRECURSOR-LIKE PROTEIN-2 DURING TROPHIC FACTOR WITHDRAWAL-INDUCED DEATH OF NEURONAL PC12 CELLS, Molecular brain research, 56(1-2), 1998, pp. 169-177
Citations number
57
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
0169328X
Volume
56
Issue
1-2
Year of publication
1998
Pages
169 - 177
Database
ISI
SICI code
0169-328X(1998)56:1-2<169:IEOAPP>2.0.ZU;2-7
Abstract
Programmed cell death (PCD) (apoptosis) is implicated in the neuronal cell death of Alzheimer's disease (AD). We investigated expression of amyloid precursor protein (APP) and amyloid precursor-like protein 2 ( APLP2) during trophic factor deprivation-induced PCD of neuronally dif ferentiated PC12 cells. Neuronal PC12 cells underwent PCD within two d ays following withdrawal of nerve growth factor (NGF) from the culture medium. Total APP mRNA levels increased gradually after 24 h, reachin g levels 250% higher than those in control cells at 48 h after NGF wit hdrawal, and total APLP2 mRNA levels also increased similarly at 48 h. Analysis of the three major APP mRNA isoforms APP695, APP751, and APP 770 by reverse transcription polymerase chain reaction showed a substa ntial increase in the proportion of APP770 at 48 h after NGF withdrawa l. Basic fibroblast growth factor, which prevented the appearance of P CD after NGF withdrawal, inhibited the increases in APP and APLP2 mRNA levels as well as the increase in the proportion of APP770. Cellular holoprotein levels of total APP, APP containing the Kunitz protease in hibitor domain, and APLP2 also increased by similar to 60%, 100%, and 30%, respectively, at 48 h after NGF withdrawal. These data indicate t hat in neuronal PC12 cells undergoing PCD following trophic factor wit hdrawal, the syntheses of both APP and APLP2 are upregulated, and the alternative splicing of the APP gene is modified. This implies a linka ge between APP and APLP2 expression and neuronal PCD. (C) 1998 Elsevie r Science B.V.