α- and β-secretase:: profound changes in Alzheimer's disease
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作者:
Tyler, SJ
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机构:Univ Bristol, Bristol Royal Infirm, Mol Neurobiol Unit, URCN Care Elderly, Bristol BS2 8HW, Avon, England
Tyler, SJ
Dawbarn, D
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机构:Univ Bristol, Bristol Royal Infirm, Mol Neurobiol Unit, URCN Care Elderly, Bristol BS2 8HW, Avon, England
Dawbarn, D
Wilcock, GK
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机构:Univ Bristol, Bristol Royal Infirm, Mol Neurobiol Unit, URCN Care Elderly, Bristol BS2 8HW, Avon, England
Wilcock, GK
Allen, SJ
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Univ Bristol, Bristol Royal Infirm, Mol Neurobiol Unit, URCN Care Elderly, Bristol BS2 8HW, Avon, EnglandUniv Bristol, Bristol Royal Infirm, Mol Neurobiol Unit, URCN Care Elderly, Bristol BS2 8HW, Avon, England
Allen, SJ
[1
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机构:
[1] Univ Bristol, Bristol Royal Infirm, Mol Neurobiol Unit, URCN Care Elderly, Bristol BS2 8HW, Avon, England
[2] Frenchay Hosp, Dept Care Elderly, Bristol BS16 1LE, Avon, England
The amyloid plaque, a neuropathological hallmark of Alzheimer's disease, is produced by the deposition of beta-amyloid (Abeta) peptide, which is cleaved from Amyloid Precursor Protein (APP) by the enzyme beta-secretase. Only small amounts of Abeta form in normal brain; more typically this is precluded by the processing of APP by alpha-secretase. Here, we describe a decrease in alpha-secretase (81% of normal) and a large increase in beta-secretase activity (185%) in sporadic Alzheimer's disease temporal cortex. Since alpha-secretase is present principally in neurons known to be vulnerable in Alzheimer's disease, and there is known competition between alpha- and beta-secretase for the substrate APP, it is significant that the majority of Alzheimer samples tested here were low in a-secretase. Eighty percent of Alzheimer brains examined had an increase in beta-secretase, a decrease in alpha-secretase, or both; which may account for the means by which the majority of people develop Alzheimer's disease. (C) 2002 Elsevier Science (USA). All rights reserved.
机构:
Mem Sloan Kettering Canc Ctr, Chem Biol Program, New York, NY 10065 USA
Cornell Univ, Weill Grad Sch, Program Pharmacol, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Chem Biol Program, New York, NY 10065 USA
Luo, Joanna E.
Li, Yue-Ming
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Mem Sloan Kettering Canc Ctr, Chem Biol Program, New York, NY 10065 USA
Cornell Univ, Weill Grad Sch, Program Pharmacol, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Chem Biol Program, New York, NY 10065 USA
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Univ La Frontera, Dept Ciencias Basicas, Av Francisco Salazar 01145,Casilla 54-D, Temuco 4811230, ChileUniv La Frontera, Dept Ciencias Basicas, Av Francisco Salazar 01145,Casilla 54-D, Temuco 4811230, Chile
Miranda, Alvaro
Montiel, Enrique
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Univ La Frontera, Dept Ciencias Basicas, Av Francisco Salazar 01145,Casilla 54-D, Temuco 4811230, ChileUniv La Frontera, Dept Ciencias Basicas, Av Francisco Salazar 01145,Casilla 54-D, Temuco 4811230, Chile
Montiel, Enrique
Ulrich, Henning
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Univ Sao Paulo, Inst Quim, Dept Bioquim, Av Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP, BrazilUniv La Frontera, Dept Ciencias Basicas, Av Francisco Salazar 01145,Casilla 54-D, Temuco 4811230, Chile
Ulrich, Henning
Paz, Cristian
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Univ La Frontera, Dept Ciencias Basicas, Av Francisco Salazar 01145,Casilla 54-D, Temuco 4811230, ChileUniv La Frontera, Dept Ciencias Basicas, Av Francisco Salazar 01145,Casilla 54-D, Temuco 4811230, Chile