The cytoplasmic sequence of E‐cadherin promotes non‐amyloidogenic degradation of Aβ precursors

• Published in: Journal of neurochemistry Vol. 96; no. 4; pp. 1182 - 1188
• Main Authors: Agiostratidou, Georgia, Muros, Rosa Miñana, Shioi, Junichi, Marambaud, Philippe, Robakis, Nikolaos K.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Ltd 01-02-2006; Blackwell
• Subjects: Abeta; Alzheimer's disease; Amyloid beta-Protein Precursor - metabolism; Amyloid Precursor Protein Secretases; Animals; Binding Sites; Biological and medical sciences; Cadherins - chemistry; Cadherins - physiology; Cell physiology; CHO Cells; Cricetinae; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Endopeptidases - metabolism; E‐cadherin; Fundamental and applied biological sciences. Psychology; lysosomal/endosomal system; Medical sciences; Miscellaneous; Molecular and cellular biology; Neurology; presenilin; Recombinant Proteins - metabolism; Transfection; γ‐secretase; Transmembrane protein; lysosomal/endosomal system; Nervous system diseases; Peptides; Alzheimer disease; Cadherin; Precursor; E-cadherin; Amyloid precursor protein; Cerebral disorder; Abeta; presenilin; Central nervous system disease; Degenerative disease; Intracellular; γ-secretase; Alzheimer's disease; Biological receptor
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1111/j.1471-4159.2005.03616.x

The presenilin (PS)/γ‐secretase system promotes production of the Abeta (Aβ) peptides by mediating cleavage of amyloid precursor protein (APP) at the γ‐sites. This system is also involved in the processing of type‐I transmembrane proteins, including APP, cadherins and Notch1 receptors, at the ɛ‐cleavage site, resulting in the production of peptides containing the intracellular domains (ICDs) of the cleaved proteins. Emerging evidence shows that these peptides have important biological functions, raising the possibility that their inhibition by γ‐secretase inhibitors may be detrimental to the cell. Here, we show that peptide E‐Cad/CTF2, produced by the PS1/γ‐secretase processing of E‐cadherin, promotes the lysosomal/endosomal degradation of the transmembrane APP derivatives, C99 and C83, and inhibits production of the APP ICD (AICD). In addition, E‐Cad/CTF2 decreases accumulation of total secreted Aβ. These data suggest a novel method to promote the non‐amyloidogenic degradation of Aβ precursors and to inhibit Aβ production.