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beta-Secretase, APP and Abeta in Alzheimer's disease.
Subcell Biochem. 2005; 38:79-103.SB

Abstract

Amyloid plaques, hallmark neuropathological lesions in Alzheimer's disease (AD) brain, are composed of the beta-amyloid peptide (Abeta). A large body of evidence suggests Abeta is central to the pathophysiology of AD and is likely to start this intractable neurodegenerative disorder. Mutations in three genes (amyloid precursor protein/APP, presenilin1, presenilin2) cause early on-set familial AD by increasing synthesis of the toxic 42 amino acid species of Abeta (Abeta42). Fibrillar Abeta in amyloid plaques appears to cause neurodegeneration, although recent studies suggest soluble Abeta oligomers may also be neurotoxic. Regardless, given the strong correlation between Abeta and AD, therapeutic strategies to lower cerebral Abeta levels should prove beneficial for the treatment of AD. Abeta is derived from APP via cleavage by two proteases, beta- and gamma-secretase. beta-secretase, recently identified as the novel aspartic protease BACEI, initiates the formation of Abeta. Consequently, BACE1 in principle is an excellent therapeutic target for strategies to reduce the production of Abeta in AD. However, the discovery of the homologue BACE2 raised the question of whether it too may be a beta-secretase. To settle this issue, our group and others have used gene targeting to generate BACE1 deficient (knockout) mice. These BACEI knockout mice have been instrumental in validating BACEI as the authentic beta-secretase in vivo. Here, I review the roles of BACE1, APP, and Abeta in AD and discuss the implications of therapeutic approaches that target BACE1 for the treatment of AD.

Authors+Show Affiliations

Department of Cell and Molecular Biology, The Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

15709474

Citation

Vassar, Robert. "Beta-Secretase, APP and Abeta in Alzheimer's Disease." Sub-cellular Biochemistry, vol. 38, 2005, pp. 79-103.
Vassar R. Beta-Secretase, APP and Abeta in Alzheimer's disease. Subcell Biochem. 2005;38:79-103.
Vassar, R. (2005). Beta-Secretase, APP and Abeta in Alzheimer's disease. Sub-cellular Biochemistry, 38, 79-103.
Vassar R. Beta-Secretase, APP and Abeta in Alzheimer's Disease. Subcell Biochem. 2005;38:79-103. PubMed PMID: 15709474.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - beta-Secretase, APP and Abeta in Alzheimer's disease. A1 - Vassar,Robert, PY - 2005/2/16/pubmed PY - 2005/4/13/medline PY - 2005/2/16/entrez SP - 79 EP - 103 JF - Sub-cellular biochemistry JO - Subcell Biochem VL - 38 N2 - Amyloid plaques, hallmark neuropathological lesions in Alzheimer's disease (AD) brain, are composed of the beta-amyloid peptide (Abeta). A large body of evidence suggests Abeta is central to the pathophysiology of AD and is likely to start this intractable neurodegenerative disorder. Mutations in three genes (amyloid precursor protein/APP, presenilin1, presenilin2) cause early on-set familial AD by increasing synthesis of the toxic 42 amino acid species of Abeta (Abeta42). Fibrillar Abeta in amyloid plaques appears to cause neurodegeneration, although recent studies suggest soluble Abeta oligomers may also be neurotoxic. Regardless, given the strong correlation between Abeta and AD, therapeutic strategies to lower cerebral Abeta levels should prove beneficial for the treatment of AD. Abeta is derived from APP via cleavage by two proteases, beta- and gamma-secretase. beta-secretase, recently identified as the novel aspartic protease BACEI, initiates the formation of Abeta. Consequently, BACE1 in principle is an excellent therapeutic target for strategies to reduce the production of Abeta in AD. However, the discovery of the homologue BACE2 raised the question of whether it too may be a beta-secretase. To settle this issue, our group and others have used gene targeting to generate BACE1 deficient (knockout) mice. These BACEI knockout mice have been instrumental in validating BACEI as the authentic beta-secretase in vivo. Here, I review the roles of BACE1, APP, and Abeta in AD and discuss the implications of therapeutic approaches that target BACE1 for the treatment of AD. SN - 0306-0225 UR - https://www.unboundmedicine.com/medline/citation/15709474/beta_Secretase_APP_and_Abeta_in_Alzheimer's_disease_ L2 - https://medlineplus.gov/alzheimersdisease.html DB - PRIME DP - Unbound Medicine ER -