نتایج جستجو برای: secretase

تعداد نتایج: 3434  

2005
Kulandaivelu S. Vetrivel Haipeng Cheng Seong-Hun Kim Ying Chen Natalie Y. Barnes Angèle T. Parent Sangram S. Sisodia Gopal Thinakaran

-Secretase facilitates the regulated intramembrane proteolysis of select type I membrane proteins that play diverse physiological roles in multiple cell types and tissue. In this study, we used biochemical approaches to examine the distribution of amyloid precursor protein (APP) and several additional -secretase substrates in membrane microdomains. We report that APP C-terminal fragments (CTFs)...

Journal: :Neuron 2006
Laura E. Doglio Ritu Kanwar George R. Jackson Mar Perez Jesús Avila Colin Dingwall Carlos G. Dotti Mark E. Fortini Fabián Feiguin

Genetic analysis of familial Alzheimer's disease has revealed that mutations in the gamma-secretase enzyme presenilin promote toxic Abeta secretion; however, presenilin mutations might also influence tau hyperphosphorylation and neurodegeneration through gamma-secretase-independent mechanisms. To address this possibility and determine whether other components of the gamma-secretase complex poss...

2016
David M Bolduc Daniel R Montagna Matthew C Seghers Michael S Wolfe Dennis J Selkoe

γ-secretase is responsible for the proteolysis of amyloid precursor protein (APP) into short, aggregation-prone amyloid-beta (Aβ) peptides, which are centrally implicated in the pathogenesis of Alzheimer's disease (AD). Despite considerable interest in developing γ-secretase targeting therapeutics for the treatment of AD, the precise mechanism by which γ-secretase produces Aβ has remained elusi...

2017
Frank Raven Joseph F. Ward Katarzyna M. Zoltowska Yu Wan Enjana Bylykbashi Sean J. Miller Xunuo Shen Se Hoon Choi Kevin D. Rynearson Oksana Berezovska Steven L. Wagner Rudolph E. Tanzi Can Zhang

A central pathogenic event of Alzheimer's disease (AD) is the accumulation of the Aβ42 peptide, which is generated from amyloid-β precursor protein (APP) via cleavages by β- and γ-secretase. We have developed a class of soluble 2-aminothiazole γ-secretase modulators (SGSMs) that preferentially decreases Aβ42 levels. However, the effects of SGSMs in AD animals and cells expressing familial AD mu...

2014
Xian Zhang Yanfang Li Huaxi Xu Yun-wu Zhang

One of the most critical pathological features of Alzheimer's disease (AD) is the accumulation of β-amyloid (Aβ) peptides that form extracellular senile plaques in the brain. Aβ is derived from β-amyloid precursor protein (APP) through sequential cleavage by β- and γ-secretases. γ-secretase is a high molecular weight complex minimally composed of four components: presenilins (PS), nicastrin, an...

2012
Jung-Soon Mo Ji-Hye Yoon Ji-Ae Hong Mi-Yeon Kim Eun-Jung Ann Ji-Seon Ahn Su-Man Kim Hyeong-Jin Baek Florian Lang Eui-Ju Choi Hee-Sae Park

The gamma-secretase complex is involved in the intramembranous proteolysis of a variety of substrates, including the amyloid precursor protein and the Notch receptor. Nicastrin (NCT) is an essential component of the gamma-secretase complex and functions as a receptor for gamma-secretase substrates. In this study, we determined that serum- and glucocorticoid-induced protein kinase 1 (SGK1) marke...

Journal: :Cell 2005
Sanjiv Shah Sheu-Fen Lee Katsuhiko Tabuchi Yi-Heng Hao Cong Yu Quincey LaPlant Haydn Ball Charles E. Dann Thomas Südhof Gang Yu

-secretase catalyzes the intramembrane cleavage of amyloid precursor protein (APP) and Notch after their extracellular domains are shed by site-specific proteolysis. Nicastrin is an essential glycoprotein component of the -secretase complex but has no known function. We now show that the ectodomain of nicastrin binds the new amino terminus that is generated upon proteolysis of the extracellular...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
S Sinha I Lieberburg

The major constituent of senile plaques in Alzheimer's disease is a 42-aa peptide, referred to as beta-amyloid (Abeta). Abeta is generated from a family of differentially spliced, type-1 transmembrane domain (TM)-containing proteins, called APP, by endoproteolytic processing. The major, relatively ubiquitous pathway of APP metabolism in cell culture involves cleavage by alpha-secretase, which c...

Journal: :iranian journal of child neurology 0
adwait bhadbhade graduate student, department of biology, california state university, fresno, ca,usa davis weizhong cheng research associate professor, medical research infrastructure for minority institutions & department of biology, california state university, fresno, usa

how to cite this article: bhadbhade a, cheng dw. amyloid precursor protein processing in alzheimer’s disease. iranian journal of child neurology2012;6(1):1-5. alzheimer’s disease (ad) is a progressive neurodegenerative disorder and a leading cause of dementia. the ad is characterized by presence of intraneuronal tangles and extracellular plaques in the brain. the plaques are composed of dense a...

2008
Michael S Wolfe

The amyloid-β peptide (Aβ), implicated in the pathogenesis of Alzheimer's disease (AD), is produced through sequential proteolysis of the Aβ precursor protein (APP) by βand γ-secretases. Thus, blocking either of these two proteases, directly or indirectly, is potentially worthwhile toward developing AD therapeutics. β-Secretase is a membrane-tethered pepsin-like aspartyl protease suitable for s...

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