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Histochemically reactive zinc in plaques of the Swedish mutant beta-amyloid precursor protein transgenic mice.

Authors
Lee, JY; Mook-Jung, I; Koh, JY
Citation
The Journal of neuroscience : the official journal of the Society for Neuroscience, 19(11):RC10-RC10, 1999
Journal Title
The Journal of neuroscience : the official journal of the Society for Neuroscience
ISSN
0270-64741529-2401
Abstract
Endogenous metals such as zinc may contribute to beta-amyloid (Abeta) aggregation and hence the plaque formation. In the present study, we examined brains of four Swedish mutant amyloid precursor protein (APP) transgenic mice at 12 months of age for histochemically reactive zinc in the plaques. Here, we report that all the Congo red (+) mature plaques contained chelatable zinc, as demonstrated by staining with the zinc-specific fluorescent dye 6-methoxy-8-quinolyl-para-toluenesulfonamide (TSQ). On the other hand, Congo red (-) preamyloid Abeta deposits were not stained with TSQ. Interestingly, although cerebellum contained similar degree of preamyloid Abeta deposits as cerebral cortex, it was completely devoid of Congo red- or TSQ-stained mature plaques. Although zinc from plaques was only slowly and partially removed by a specific zinc remover, dithizone, treatment of brain sections with heparinase-III, which degrades heparan sulfate proteoglycan (HSPG), another major constituent of plaques, greatly fastened the zinc removal with dithizone. The present study has demonstrated the presence of histochemically reactive zinc in plaques, but not preamyloid Abeta deposits, of the Swedish mutant APP transgenic mice. Because preamyloid Abeta deposits fail to develop into congophilic plaques in cerebellum where synaptic vesicle zinc is deficient, the synaptic zinc may be a necessary element in the plaque formation. In holding zinc inside plaques, HSPG may contribute in addition to Abeta.
MeSH terms
AminoquinolinesAmyloid beta-Protein Precursor/geneticsAmyloid beta-Protein Precursor/metabolism*AnimalsColoring AgentsCongo RedFluorescent DyesImmunohistochemistryMiceMice, TransgenicMicroscopy, FluorescenceMutationPlaque, Amyloid/metabolism*Tosyl CompoundsZinc/metabolism*
PMID
10341271
Appears in Collections:
Journal Papers > Research Organization > Brain Disease Research Center
AJOU Authors
묵, 인희
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