Peripheral immune system and neuroimmune communication impairment in a mouse model of Alzheimer's disease
Neurodegenerative diseases such as Alzheimer's disease (AD) can be understood in the context of the aging of neuroimmune communication. Although the contribution to AD of the immune cells present in the brain is accepted, the role of the peripheral immune system is less well known. The present...
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Published in | Annals of the New York Academy of Sciences Vol. 1262; no. 1; pp. 74 - 84 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Malden, USA
Blackwell Publishing Inc
01.07.2012
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0077-8923 1749-6632 1749-6632 |
DOI | 10.1111/j.1749-6632.2012.06639.x |
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Summary: | Neurodegenerative diseases such as Alzheimer's disease (AD) can be understood in the context of the aging of neuroimmune communication. Although the contribution to AD of the immune cells present in the brain is accepted, the role of the peripheral immune system is less well known. The present review examines the behavior and the function and redox state of peripheral immune cells in a triple‐transgenic mouse model (3×Tg‐AD). These animals develop both beta‐amyloid plaques and neurofibrillary tangles with a temporal‐ and regional‐specific profile that closely mimics their development in the human AD brain. We have observed age and sex‐related changes in several aspects of behavior and immune cell functions, which demonstrate premature aging. Lifestyle strategies such as physical exercise and environmental enrichment can improve these aspects. We propose that the analysis of the function and redox state of peripheral immune cells can be a useful tool for measuring the progression of AD. |
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Bibliography: | ark:/67375/WNG-D5J4WWQJ-3 ArticleID:NYAS6639 istex:81B33DEE775576EEE1EFA8C47E9A0B1940A4A5EA ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ISSN: | 0077-8923 1749-6632 1749-6632 |
DOI: | 10.1111/j.1749-6632.2012.06639.x |