Nuclear Factor-Kappa B and Alzheimer Disease, Unifying Genetic and Environmental Risk Factors from Cell to Humans

被引:103
作者
Jones, Simon Vann [1 ]
Kounatidis, Ilias [2 ]
机构
[1] Univ Oxford, Warneford Hosp, Dept Psychiat, Oxford, England
[2] Univ Oxford, Dept Biochem, Lab Cell Biol Dev & Genet, Oxford, England
基金
欧洲研究理事会;
关键词
nuclear factor-kappa B; Alzheimer; dementia; cell lines; invertebrate models; rodents; humans; INDUCED OXIDATIVE STRESS; TRAUMATIC BRAIN-INJURY; APOLIPOPROTEIN-E; CYTOKINE PRODUCTION; INSULIN-RESISTANCE; BINDING PROTEIN; FATTY-ACIDS; EXPRESSION; BETA; INFLAMMATION;
D O I
10.3389/fimmu.2017.01805
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Alzheimer's disease (AD) is the most common form of dementia, an eversible, progressive disease that causes problems with memory, thinking, language, planning, and behavior. There are a number of risk factors associated with developing AD but the exact cause remains unknown. The predominant theory is that excessive build-up of amyloid protein leads to cell death, brain atrophy, and cognitive and functional decline. However, the amyloid hypothesis has not led to a single successful treatment. The recent failure of Solanezumab, a monoclonal antibody to amyloid, in a large phase III trial was emblematic of the repeated failure of anti-amyloid therapeutics. New disease targets are urgently needed. The innate immune system is increasingly being implicated in the pathology of number of chronic diseases. This focused review will summarize the role of transcription factor nuclear factor-kappa B (NF-kappa B), a key regulator of innate immunity, in the major genetic and environmental risk factors in cellular, invertebrate and vertebrate models of AD. The paper will also explore the relationship between NF-kappa B and emerging environmental risk factors in an attempt to assess the potential for this transcription factor to be targeted for disease prevention.
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页数:9
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