Cerebral Microemboli Increase β-amyloid Protein Deposition, MMP-9, and GFAP Expression in the Alzheimer`s Model of APP/PS1 Double Transgenic Mice

ISSN: 1875-5739 (Online)
ISSN: 1567-2026 (Print)

Volume 14, 4 Issues, 2017

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Current Neurovascular Research

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Cerebral Microemboli Increase β-amyloid Protein Deposition, MMP-9, and GFAP Expression in the Alzheimer`s Model of APP/PS1 Double Transgenic Mice

Current Neurovascular Research, 11(3): 190-201.

Author(s): Min Ning, Yiying Wu, Xiushi Ni, Yanling Zhao and Rujing Ling.

Affiliation: Department of Geriatrics, Shanghai First People's Hospital, Shanghai Jiao Tong University, No. 100 Haining Road, Shanghai 200080, China.


We investigated the effects of cerebral arterial microemboli on amyloid β protein (A β) deposition in the hippocampal region of amyloid precursor protein/presenilin 1 (APP/PS1) double transgenic mice and evaluated the role of cerebral arterial microemboli in Alzheimer's disease (AD) pathogenesis.

The mice were divided into a wild-type sham surgery group (n = 15), a wild-type coupled with microemboli group (n =15), an APP/PS1 double transgenic sham surgery group (n =15) and an APP/PS1 double transgenic coupled with microemboli group (n =15). The microemboli mice were injected via the left internal carotid artery with 300 µ L of a normal saline suspension containing 100 whole blood clot-derived microemboli (25-50 µ m). The sham surgery mice were injected with equal volumes of saline. After the mouse model was established for 1, 2 or 4 weeks, the Aβ 1-42 deposition in the left hippocampal region and the matrix metalloproteinase-9 (MMP-9) and glial fibrillary acidic protein (GFAP) expression levels were determined through immunohistochemical staining.

The Aβ 1-42 deposition level in the left hippocampi of transgenic microemboli group was significantly greater than in the transgenic sham group at week 1 and 2 (P< 0.001) but not at week 4. No Aβ 1-42 deposition was detected in the wild-type groups. Only sporadic MMP-9- and GFAP-positive cells were observed in the wild-type sham group. Significantly more MMP-9- and GFAP-positive cells were detected in the transgenic groups (P<0.001), particularly in the transgenic microemboli group. An intragroup analysis of the time factor for the microemboli groups showed significantly more MMP-9- and GFAP-positive cells at week 1 than at week 2 or 4 (P< 0.001). No difference was detected between time points in the sham groups.

Cerebral microemboli increased Aβ deposition in the hippocampal region of APP/PS1 double transgenic mice. MMP-9 and GFAP expression may play an important role in excess A β deposition, which is caused by an imbalance between the protein’s synthesis and removal.


Amyloid &#946; protein, APP/PS1 double transgenic mouse, astrocyte, matrix metalloproteinase-9, microemboli.

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Article Details

Volume: 11
Issue Number: 3
First Page: 190
Last Page: 201
Page Count: 12
DOI: 10.2174/1567202611666140606104132
Price: $58

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