High Activities of BACE1 in Brains with Mild Cognitive Impairment

被引:78
作者
Cheng, Xin [1 ,2 ]
He, Ping [2 ,3 ,4 ]
Lee, Taehee [2 ]
Yao, Hailan [3 ]
Li, Rena [4 ]
Shen, Yong [1 ,2 ,3 ,5 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Neurol, State Key Lab Med Neurobiol, Shanghai 200433, Peoples R China
[2] Sun Hlth Res Inst, Haldeman Lab Mol & Cellular Neurobiol, Sun City, AZ USA
[3] Roskamp Inst, Ctr Adv Therapeut Strategies Brain Disorders, Sarasota, FL 34243 USA
[4] Roskamp Inst, Sarasota, FL 34243 USA
[5] Univ Florida, Coll Med, Dept Neurol, Gainesville, FL 32611 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
AMYLOID PRECURSOR PROTEIN; BETA-SECRETASE ACTIVITY; NECROSIS-FACTOR DEATH; ALZHEIMERS-DISEASE; NEURONAL-ACTIVITY; CONSORTIUM; EXPRESSION; DIAGNOSIS; INSTITUTE; ESTABLISH;
D O I
10.1016/j.ajpath.2013.10.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We recently discovered elevated B-secretase 1 (BACE1) activity in brains with sporadic Alzheimer disease (AD). Moreover, we also found high Levels of BACE1 enzymatic activity in the cerebrospinal fluid from patients with both mild cognitive impairment (MCI) and AD. These results suggest that elevation of BACE1 enzymatic activity may occur early or may contribute to AD. We therefore examined whether BACE1 enzymatic activity was changed in MCI brains. BACE1 activity and tumor necrosis factor (TNF)-alpha Levels were measured by enzymatic assay and ELISA in the temporal cortex from 18 patients with clinically well-characterized AD, 18 patients with MCI, and 18 healthy controls. We found a significant increase in BACE1 activity and protein Level in brains of MCI and AD patients. Moreover, increased BACE1 activity correlated with plaque numbers and cognition status. We also found an increase in TNF-alpha in MCI brains. In vitro study revealed that TNF-alpha rather than other cytokines can up-regulate BACE1 protein expression. These findings suggest that BACE1 increase occurs early in MCI and is possibly induced by TNF-alpha and that BACE1 enzymatic activity may be important for conversion of MCI to AD.
引用
收藏
页码:141 / 147
页数:7
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