Elevation of beta-amyloid peptide 2-42 in sporadic and familial Alzheimer's disease and its generation in PS1 knockout cells

Urea-based beta -amyloid (A beta) SDS-polyacrylamide gel electrophoresis an d immunoblots were used to analyze the generation of A beta peptides in con ditioned medium from primary mouse neurons and a neuroglioma cell line, as well as in human cerebrospinal fluid. A comparable and highly conserved pat tern of A beta peptides, namely, 1-40/42 and carboxyl-terminal-truncated 1- 37, 1-38, and 1-39, was found. Besides A beta1-42, we also observed a consi stent elevation of amino-terminal-truncated A beta2-42 in a detergent-solub le pool in brains of subjects with Alzheimer's disease. A beta2-42 was also specifically elevated in cerebrospinal fluid samples of Alzheimer's diseas e patients. To decipher the contribution of potential different gamma -secr etases (presenilins (PSs)) in generating the amino-terminal- and carboxyl-t erminal-truncated A beta peptides, we overexpressed. beta -amyloid precurso r protein (APP)-trafficking mutants in PS1+/+ and PS1-/- neurons. As compar ed with APP-WT (primary neurons from control or PS1-deficient mice infected with Semliki Forest virus), PS1-/- neurons and PS1+/+ neurons overexpressi ng APP-Delta ct (a slow-internalizing mutant) show a decrease of all secret ed A beta peptide species, as expected, because this mutant is processed ma inly by alpha -secretase. This drop is even more pronounced for the APP-KK construct (APP mutant carrying an endoplasmic reticulum retention motif). S urprisingly, A beta2-42 is significantly less affected in PS1-/- neurons an d in neurons transfected with the endocytosis-deficient APP-Delta ct constr uct. Our data confirm that PS1 is closely involved in the production of A b eta1-40/42 and the carboxyl-terminal-truncated A beta1-37, A beta1-38, and A beta1-39, but the amino-terminal-truncated and carboxyl-terminal-elongate d A beta2-42 seems to be less affected by PS1 deficiency. Moreover, our res ults indicate that the latter A beta peptide species could be generated by a beta (Asp/Ala)-secretase activity.