A novel microdomain-dependent regulatory mechanism of amyloid precursor protein processing
Project/Area Number |
20300125
|
Research Category |
Grant-in-Aid for Scientific Research (B)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Nerve anatomy/Neuropathology
|
Research Institution | Juntendo University |
Principal Investigator |
SAKURAI Takashi Juntendo University, 医学部, 教授 (70225845)
|
Co-Investigator(Kenkyū-buntansha) |
NUKINA Nobuyuki (独)理化学研究所, 構造神経病理研究チーム, チームリーダー (10134595)
|
Co-Investigator(Renkei-kenkyūsha) |
KASHIYAMA Taku 順天堂大学, 医学部, 助教 (90338343)
ARAYA Runa 順天堂大学, 医学部, 助教 (10391848)
KAMIKUBO Yuji 順天堂大学, 医学部, 助教 (80509670)
|
Project Period (FY) |
2008 – 2010
|
Project Status |
Completed (Fiscal Year 2010)
|
Budget Amount *help |
¥18,850,000 (Direct Cost: ¥14,500,000、Indirect Cost: ¥4,350,000)
Fiscal Year 2010: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Fiscal Year 2009: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Fiscal Year 2008: ¥13,130,000 (Direct Cost: ¥10,100,000、Indirect Cost: ¥3,030,000)
|
Keywords | 神経変性疾患 / 痴呆 / 脂質 / 脳神経疾患 |
Research Abstract |
Beta-cleavage of amyloid precursor protein (APP) by β-secretase (BACE1) in a membrane microdomain is thought to be a critical regulatory event in generating β-amyloid which is central to the pathogenesis of Alzheimer's disease. To investigate the underlying molecular mechanisms of this process, we analyzed immunoisolated, APP-containing, detergent-resistant membranes from mouse brains. APP was associated with cholesterol-dependent microdomains through a network of protein interactions involving X11, Munc18 and syntaxin 1, which largely excluded BACE1. APP-X11-Munc18 interaction mediated inhibitory effects on APP-BACE1 interaction and β-cleavage. We propose a novel regulatory mechanism of APP processing involving microdomain segregation that depends on protein-protein interactions and is controlled by cdk5 phosphorylation.
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Report
(4 results)
Research Products
(25 results)