中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Amyloid deposition and inflammation in appswe/ps1de9 mouse model of alzheimer's disease

文献类型:期刊论文

作者Ruan, Lingfei1; Kang, Zhoujun2; Pei, Gang3; Le, Yingying1
刊名Current alzheimer research
出版日期2009-12-01
卷号6期号:6页码:531-540
关键词Alzheimer's disease Appswe/ps1de9 Transgenic mouse Amyloid deposition Inflammation Microglia Astrocyte Neuron
ISSN号1567-2050
通讯作者Le, yingying(yyle@sibs.ac.cn)
英文摘要Alzheimer's disease (ad) is characterized by amyloid plaques and neurofibrillary tangles associated with chronic inflammation. appswe/ps1de9 is an ad mouse model bearing mutant transgenes of amyloid precursor protein and presenilin-1. amyloid deposition is present in this mouse model at early stage of life. however, the progression of inflammation and its relationship with amyloid deposition have not been characterized. here we showed that amyloid plaques were present at 4 months of age and increased with age. cd11b-positive microglia clusters appeared in hippocampus and neocortex at 4 months of age and increased with age. clustered glial fibrillary acidic protein (gfap)-positive astrocytes were observed in hippocampus and cortex after 6 months of age and increased with age. double staining with cd11b/gfap antibody and thioflavin s showed clustered microglia and astrocytes were in close association with amyloid plaques. expression of tnf-alpha was detected at 8 months of age, while il-1 beta il-6 and mcp-1 at 10 months. these cytokines increased with age. double immunostaining of cell specific marker and cytokine indicated tnf-alpha, il-1 beta, il-6 and mcp-1 were expressed by activated microglia and a small part of activated astrocytes. mcp-1 was also expressed by neurons, which support recent finding that mcp-1 expression was increased in neurons of ad patient. these results demonstrate amyloid plaques and its associated inflammatory response developed at early stage of life and progressively increased with age, both activated glia and neurons are involved in chronic inflammation in ad. appswe/ps1de9 model provides a mean for studying the mechanisms and novel therapeutics for ad.
WOS关键词TUMOR-NECROSIS-FACTOR ; COMPLEMENT CONTROL PROTEIN ; MONOCYTE CHEMOATTRACTANT PROTEIN-1 ; MILD COGNITIVE IMPAIRMENT ; NITRIC-OXIDE SYNTHASE ; A-BETA-DEPOSITION ; TRANSGENIC MICE ; PRECURSOR-PROTEIN ; MEMORY DEFICITS ; IN-VITRO
WOS研究方向Neurosciences & Neurology
WOS类目Clinical Neurology ; Neurosciences
语种英语
WOS记录号WOS:000271344600008
出版者BENTHAM SCIENCE PUBL LTD
URI标识http://www.irgrid.ac.cn/handle/1471x/2405172
专题中国科学院大学
通讯作者Le, Yingying
作者单位1.Chinese Acad Sci, SIBS, Inst Nutr Sci, Grad Sch,Key Lab Nutr & Metab, Shanghai 200031, Peoples R China
2.Second Mil Med Univ, Changhai Hosp, Emergency Dept, Shanghai, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol Cell Biol Lab, Shanghai 200031, Peoples R China
推荐引用方式
GB/T 7714
Ruan, Lingfei,Kang, Zhoujun,Pei, Gang,et al. Amyloid deposition and inflammation in appswe/ps1de9 mouse model of alzheimer's disease[J]. Current alzheimer research,2009,6(6):531-540.
APA Ruan, Lingfei,Kang, Zhoujun,Pei, Gang,&Le, Yingying.(2009).Amyloid deposition and inflammation in appswe/ps1de9 mouse model of alzheimer's disease.Current alzheimer research,6(6),531-540.
MLA Ruan, Lingfei,et al."Amyloid deposition and inflammation in appswe/ps1de9 mouse model of alzheimer's disease".Current alzheimer research 6.6(2009):531-540.

入库方式: iSwitch采集

来源:中国科学院大学

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。