Author/Authors :
J.A. Johnston، نويسنده , , W.W. Liu، نويسنده , , D.T.R. Coulson، نويسنده , , S. Todd، نويسنده , , S. Murphy، نويسنده , , S. Brennan، نويسنده , , C.J. Foy، نويسنده , , D. Craig، نويسنده , , G.B. Irvine، نويسنده , , A.P. Passmore، نويسنده ,
Abstract :
β-Secretase activity is the rate-limiting step in Aβ peptide production from amyloid precursor protein. Aβ is a major component of Alzheimerʹs disease (AD) cortical amyloid plaques. β-Secretase activity is elevated in post mortem brain tissue in AD. The current study investigated whether β-secretase activity was also elevated in peripheral blood platelets. We developed a novel fluorimetric β-secretase activity assay to investigate platelets isolated from individuals with AD (n = 86), and age-matched controls (n = 115). Platelet membrane β-secretase activity (expressed as initial rate) varied over fourfold between individuals, raising important questions about in vivo regulation of this proteolytic activity. Nonetheless, we identified a significant 17% increase in platelet membrane β-secretase activity in individuals with AD compared to controls (p = 0.0003, unpaired t-test). Platelet membrane β-secretase activity did not correlate with mini-mental state examination (MMSE) score in the AD group (mean MMSE = 17.7, range 1–23), indicating that the increase did not occur as a secondary result of the disease process, and may even have preceded symptom onset.
Keywords :
protease , blood , amyloid precursor protein , Neurodegeneration , biomarker , a