Monocyte Chemoattractant Protein-1 Plays a Dominant Role in the Chronic Inflammation Observed in Alzheimer's Disease

被引:190
作者
Sokolova, Anna [1 ]
Hill, Michelle D. [1 ]
Rahimi, Farid [1 ]
Warden, Lolita A. [1 ]
Halliday, Glenda M. [1 ]
Shepherd, Claire E. [1 ]
机构
[1] Prince Wales Med Res Inst, Sydney, NSW 2031, Australia
基金
英国医学研究理事会;
关键词
Alzheimer's Disease; inflammation; Monocyte Chemotactic Protein-1; MILD COGNITIVE IMPAIRMENT; NECROSIS-FACTOR-ALPHA; GENE-EXPRESSION; PRESENILIN-1; MUTATIONS; RECEPTOR ANTAGONIST; PLAQUE-FORMATION; NEURONAL LOSS; BRAIN; CHEMOKINE; BETA;
D O I
10.1111/j.1750-3639.2008.00188.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic neuroinflammation correlates with cognitive decline and brain atrophy in Alzheimer's disease (AD), and cytokines and chemokines mediate the inflammatory response. However, quantitation of cytokines and chemokines in AD brain tissue has only been carried out for a small number of mediators with variable results. We simultaneously quantified 17 cytokines and chemokines in brain tissue extracts from controls (n = 10) and from patients with and without genetic forms of AD (n = 12). Group comparisons accounting for multiple testing revealed that monocyte chemoattractant protein-1 (MCP-1), interleukin-6 (IL-6) and interleukin-8 (IL-8) were consistently upregulated in AD brain tissue. Immunohistochemistry for MCP-1, IL-6 and IL-8 confirmed this increase and determined localization of these factors in neurons (MCP-1, IL-6, IL-8), astrocytes (MCP-1, IL-6) and plaque pathology (MCP-1, IL-8). Logistic linear regression modeling determined that MCP-1 was the most reliable predictor of disease. Our data support previous work on significant increases in IL-6 and IL-8 in AD but indicate that MCP-1 may play a more dominant role in chronic inflammation in AD.
引用
收藏
页码:392 / 398
页数:7
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