Increased cystatin C in astrocytes of transgenic mice expressing the K670N-M671L mutation of the amyloid precursor protein and deposition in brain amyloid plaques

Cystatin C is an essential secretory cofactor for neurogenesis with potent protease inhibitor activities. Polymorphisms of cystatin C are genetically associated with Alzheimer's disease (AD), and the L68Q mutation causes here ditary cerebral hemorrhage with amyloidosis of the Icelandic type, in which cystatin C and beta -amyloid are colocalized in cortical blood vessels. To determine whether cystatin C and beta -amyloid also colocalize in brain am yloid plaques, we analyzed transgenic mice expressing the Swedish APP (SweA PP) mutation. We found high levels of cystatin C in astrocytes surrounding beta -amyloid plaques, and discrete layers of cystatin C attached to amyloi d plaque cores covered by a layer of beta -amyloid. In addition, cystatin C accumulated in reactive astrocytes throughout the brain, independently of, and before the onset of, amyloid plaque formation. These results show that expression of SweAPP is associated with increased cystatin C in reactive a strocytes, and they suggest an early role of cystatin C in appositional amy loid plaque growth. (C) 2001 Academic Press.