Generation of the β-Amyloid Peptide and the Amyloid Precursor Protein C-terminal Fragment γ Are Potentiated by FE65L1

• Published in: The Journal of biological chemistry Vol. 278; no. 51; pp. 51100 - 51107
• Main Authors: Chang, Yang, Tesco, Giuseppina, Jeong, William J., Lindsley, Loren, Eckman, Elizabeth A., Eckman, Christopher B., Tanzi, Rudolph E., Guénette, Suzanne Y.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 19.12.2003
• Subjects: Adaptor Proteins, Signal Transducing; Amino Acid Sequence; Amyloid beta-Peptides - biosynthesis; Amyloid beta-Protein Precursor - biosynthesis; Amyloid beta-Protein Precursor - metabolism; Amyloid Precursor Protein Secretases; Aspartic Acid Endopeptidases; Carrier Proteins - metabolism; Carrier Proteins - physiology; Cell Line, Tumor; Endopeptidases - metabolism; endosomes; Endosomes - metabolism; FE65 protein; FE65L1 protein; Humans; Membrane Proteins - biosynthesis; Organelles - metabolism; Protein Binding; Protein Processing, Post-Translational; Receptors, Notch
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M309561200

Members of the FE65 family of adaptor proteins, FE65, FE65L1, and FE65L2, bind the C-terminal region of the amyloid precursor protein (APP). Overexpression of FE65 and FE65L1 was previously reported to increase the levels of α-secretase-derived APP (APPsα). Increased β-amyloid (Aβ) generation was also observed in cells showing the FE65-dependent increase in APPsα. To understand the mechanism for the observed increase in both Aβ and APPsα given that α-secretase cleavage of a single APP molecule precludes Aβ generation, we examined the effects of FE65L1 overexpression on APP C-terminal fragments (APP CTFs). Our data show that FE65L1 potentiates γ-secretase processing of APP CTFs, including the amyloidogenic CTF C99, accounting for the ability of FE65L1 to increase generation of APP C-terminal domain and Aβ40. The FE65L1 modulation of these processing events requires binding of FE65L1 to APP and APP CTFs and is not because of a direct effect on γ-secretase activity, because Notch intracellular domain generation is not altered by FE65L1. Furthermore, enhanced APP CTF processing can be detected in early endosome vesicles but not in endoplasmic reticulum or Golgi membranes, suggesting that the effects of FE65L1 occur at or near the plasma membrane. Finally, although FE65L1 increases APP C-terminal domain production, it does not mediate the APP-dependent transcriptional activation observed with FE65.