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Expression of human beta-secretase in the mouse brain increases the steady-state level of beta-amyloid.

beta-Site APP-cleaving enzyme (BACE) initiates the processing of the amyloid precursor protein (APP) leading to the generation of beta-amyloid, the main component of Alzheimer's disease senile plaques. BACE (Asp2, memapsin 2) is a type I transmembrane aspartyl protease and is responsible for the beta-secretase cleavage of APP producing different endoproteolytic fragments referred to as the carboxy-terminal C99, C89 and the soluble ectodomain sAPPbeta. Here we describe two transgenic mouse lines expressing human BACE in the brain. Overexpression of BACE augments the amyloidogenic processing of APP as demonstrated by decreased levels of full-length APP and increased levels of C99 and C89 in vivo. In mice expressing huBACE in addition to human APP wild-type or carrying the Swedish mutation, the induction of APP processing characterized by elevated C99, C89 and sAPPbeta, results in increased brain levels of beta-amyloid peptides Abeta40 and Abeta42 at steady-state.

Pubmed ID: 11948243


  • Bodendorf U
  • Danner S
  • Fischer F
  • Stefani M
  • Sturchler-Pierrat C
  • Wiederhold KH
  • Staufenbiel M
  • Paganetti P


Journal of neurochemistry

Publication Data

March 11, 2002

Associated Grants


Mesh Terms

  • Amyloid Precursor Protein Secretases
  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Animals
  • Aspartic Acid Endopeptidases
  • Blotting, Western
  • Brain
  • Endopeptidases
  • Gene Expression
  • Humans
  • In Situ Hybridization
  • Mice
  • Mice, Transgenic
  • Mutation
  • Neurons
  • Peptide Fragments
  • Protein Processing, Post-Translational
  • RNA, Messenger
  • Transgenes