Influence of inhibited α7 nicotinic acetylcholine receptor gene expression on the production of β-amyloid peptide in SH-SY5Y cells.
- Author:
Kai OUYANG
1
;
Xiao-lan QI
;
Zhi-zhong GUAN
Author Information
- Publication Type:Journal Article
- MeSH: Amyloid Precursor Protein Secretases; genetics; metabolism; Amyloid beta-Peptides; metabolism; Aspartic Acid Endopeptidases; genetics; metabolism; Cell Line, Tumor; Humans; Neuroblastoma; metabolism; pathology; Peptide Fragments; metabolism; RNA Interference; RNA, Messenger; metabolism; RNA, Small Interfering; genetics; Receptors, Nicotinic; genetics; metabolism; Transfection; alpha7 Nicotinic Acetylcholine Receptor
- From: Chinese Journal of Pathology 2012;41(12):837-841
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the influence of inhibited α7 neuronal nicotinic acetylcholine receptor (nAChR) by small interference RNA (siRNA) in SH-SY5Y cells and to explore the connection of these changes with the β-amyloid precursor protein (APP) metabolism and the pathogenesis of Alzheimer's disease (AD).
METHODSThe siRNA of α7 nAChR was transfected into SH-SY5Y cells, and the expression of α7 nAChR and two subtypes of β-secretases (BACE1 and BACE2) at mRNA and protein levels was studied by real-time PCR and Western blot, respectively. The variation of Aβ(1-42) content was detected by ELISA.
RESULTSAs compared with controls, the expression of α7 nAChR at mRNA and protein levels in the SH-SY5Y cells transfected with the α7 nAChR siRNA were decreased by 84% and 79% (P < 0.01), respectively. The expressions of BACE1 mRNA and protein levels was increased by 527% and 71% (P < 0.01), respectively, while the expression of BACE2 decreased by 58% and 75% (P < 0.01), respectively. The Aβ(1-42) content increased by 208% (P < 0.01).
CONCLUSIONSAn inhibited α7 nAChR mRNA induced by siRNA may markedly stimulate the production of Aβ through the mechanism of increased expression of BACE1 and inhibited expression of BACE2, which may be related to the pathogenesis of AD.
