| Literature DB >> 29172001 |
Ramasamy Thangavel1,2, Sachin M Bhagavan1, Swathi Beladakere Ramaswamy1, Spurthi Surpur1, Raghav Govindarajan1, Duraisamy Kempuraj1,2, Smita Zaheer1, Sudhanshu Raikwar1, Mohammad E Ahmed1, Govindhasamy Pushpavathi Selvakumar1,2, Shankar S Iyer1, Asgar Zaheer1,2.
Abstract
Apolipoprotein E4 (ApoE4) is a major genetic risk factor for Alzheimer's disease (AD). The E4 allele of ApoE plays a crucial role in the inflammatory and neurodegenerative processes associated with AD. This is evident from the multiple effects of the ApoE isoforms in amyloid-β (Aβ) aggregation. Glia maturation factor (GMF) is a brain-specific neuroinflammatory protein that we have previously demonstrated to be significantly upregulated in various regions of AD brains compared to non-AD control brains and that it induces neurodegeneration. We have previously reported that GMF is predominantly expressed in the reactive astrocytes surrounding amyloid plaques (APs) in AD brain. In the present study, using immunohistochemical and dual immunofluorescence staining, we show the expression and colocalization of GMF and ApoE4 in AD brains. Our results show that ApoE4 is present within the APs of AD brain. Further, we found that GMF and ApoE4 were strongly expressed and co-associated in APs and in the reactive astrocytes surrounding APs in AD. An increased expression of GMF in APs and neurofibrillary tangles in the AD brain, and the co-localization of GMF and ApoE4 in APs suggest that GMF and ApoE4 together should be contributing to the neuropathological changes associated with AD.Entities:
Keywords: Alzheimer’s disease; amyloid plaques; apolipoprotein E4; neurofibrillary tangles; neuroinflammation
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Year: 2018 PMID: 29172001 PMCID: PMC5770144 DOI: 10.3233/JAD-170777
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472