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Acceleration of amyloidogenesis and memory impairment by estrogen deficiency through NF-kappa B dependent beta-secretase activation in presenilin 2 mutant mice

机译:早老素2突变小鼠中通过NF-κB依赖的β-分泌酶激活,雌激素缺乏引起的淀粉样蛋白生成和记忆障碍

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Nearly 7-10 million people are living with Alzheimer's disease (AD) worldwide. Senile plaques composed of beta-amyloid (A beta) are a pathological hallmark of Alzheimer's disease. Presenilin 2 (PS2) mutations increase A beta generation in the brains of AD patients. The A beta is generated through the sequential cleavage of amyloid precursor protein by beta- and gamma-secretases. Additionally, increasing evidences suggest that estrogen can reduce the development of AD via regulation of beta-secretases activity and beta-site APP-cleaving enzyme (BACE1) expression. But the underlying correlation mechanism of A beta generation by PS2 mutations and estrogen remains to be clarified. To investigate the anti-amyloidogenesis effect of estrogen in a PS2 mutative condition, we examined memory impairment in ovariectomized PS2 mutation (N141I) mice in which cognitive function was assessed by the Morris water maze test and passive avoidance test. In addition, Western blot analysis, immunostaining, immunofluorescence staining, ELISA and enzyme activity assays were used to examine the degree of A beta deposition in the brains. In the present study, A beta accumulated more in the ovariectomized PS2 mutant mice brain, and greatly worsened memory impairment and glial activation as well as neurogenic inflammation. In parallel with increased memory impairment, activity of beta-secretase and expression of the BACE1 increased in ovariectomized PS2 mutant mice. Much higher activity of NF-kappa B was observed by EMSA in ovariectomized PS2 mutant mice. In addition, the A beta level was decreased by treatment of beta-estradiol through inhibiting BACE1 expression in PS2 transfacted PC12 cells. These results suggest that mutation of PS2 can lead to NF-kappa B mediate amyloidogensis, and this effect can be amplified by the absence of estrogen. (C) 2015 Elsevier Inc. All rights reserved.
机译:全世界有将近7-10百万人患有阿尔茨海默氏病(AD)。由β-淀粉样蛋白(A beta)组成的老年斑是阿尔茨海默氏病的病理标志。早老素2(PS2)突变增加AD患者大脑中的A beta生成。通过β-和γ-分泌酶顺序切割淀粉样蛋白前体蛋白来生成Aβ。此外,越来越多的证据表明,雌激素可以通过调节β-分泌酶活性和β-位APP裂解酶(BACE1)的表达来减少AD的发展。但是,由PS2突变和雌激素产生A beta的潜在相关机制尚待阐明。为了研究雌激素在PS2突变条件下的抗淀粉样蛋白生成作用,我们检查了卵巢切除的PS2突变(N141I)小鼠的记忆障碍,其中莫里斯水迷宫测试和被动回避测试评估了认知功能。另外,使用蛋白质印迹分析,免疫染色,免疫荧光染色,ELISA和酶活性测定法检查大脑中Aβ沉积的程度。在本研究中,Aβ在去卵巢的PS2突变小鼠的大脑中积聚更多,大大恶化了记忆障碍和神经胶质激活以及神经源性炎症。与增加的记忆障碍同时,在卵巢切除的PS2突变小鼠中,β-分泌酶的活性和BACE1的表达增加。 EMSA在去卵巢的PS2突变小鼠中观察到了更高的NF-κB活性。此外,通过抑制PS2转染的PC12细胞中BACE1的表达,通过治疗β-雌二醇可降低A beta的水平。这些结果表明,PS2的突变可导致NF-κB介导淀粉样蛋白生成,并且这种作用可因缺乏雌激素而放大。 (C)2015 Elsevier Inc.保留所有权利。

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