β-Amyloid deposition and tau phosphorylation in clinically characterized aged cats

The current study describes both Aβ and tau abnormalities that accumulate in the brains of aged (16–21 years), but not young (<4 years) clinically characterized cats. Diffuse plaques that were morphologically different from what is typically observed in the human brain could be detected with 4G8 (Aβ17–24) or an Aβ1–42-specific antibody but not with N-terminal Aβ or an Aβ1–40-specific antibody. SELDI-TOF mass spectrometry experiments indicated that cat brain Aβ consisted almost entirely of Aβ1–42. Markers of tau hyperphosphorylation (AT8 and PHF-1) labeled a subset of neurons in two aged animals. In the hilus of the hippocampus, a subset of AT8 positive neurons showed a sprouting morphology similar to that observed in human brain. Western blot analysis with antibodies against hyperphosphorylated tau indicated that tau is hyperphosphorylated in the aged cat and contains many of the same epitopes found in Alzheimerʹs disease (AD) brain. Thus, the aged cat brain develops AD-related lesions with important morphological and biochemical differences compared to human brain.