Methylation differences in Alzheimer's disease neuropathologic change in the aged human brain.

Methylation differences in Alzheimer's disease neuropathologic change in the aged human brain.
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DOI:
10.1186/s40478-022-01470-0
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发表时间:
2022-11-29
影响因子:
7.1
通讯作者:
--
中科院分区:
医学2区
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--
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阿尔茨海默病(AD)是痴呆症的最常见原因,年龄增长是其最大的风险因素。AD神经病理学改变(ADNC)已知与人类大脑中的许多DNA甲基化改变相关,但迄今为止,在ADNC的表观遗传学研究中,年龄最大的老年人(> 90岁)的代表性不足。我们的研究参与者是来自90+研究的90岁以上的个体(n = 47)。我们分析了8个精确解剖的人脑区域的大量样本的DNA甲基化:额中回,扣带回,内嗅皮层,齿状回,CA 1,黑质,蓝斑和小脑皮层。我们使用计算方法将批量数据解卷积为细胞类型特异性(CTS)信号。在不同水平的ADNC中分析CTS甲基化差异。在齿状回中发现了最高量的ADNC相关甲基化差异,这是迄今为止在大规模多组学研究中代表性不足的区域。在齿状回神经元中,随着β淀粉样蛋白(Aβ)斑块负荷的增加,蛋白编码基因5897个启动子区域的DNA甲基化显著不同。其中,较高的Aβ斑块负荷与早老素增强子2(PEN-2)基因的启动子低甲基化相关,该基因是γ-分泌酶形成的限速基因之一,γ-分泌酶是一种多组分复合物,部分负责淀粉样前体蛋白内切蛋白水解裂解为Aβ肽。除了新的ADNC相关的DNA甲基化变化,我们目前最详细的阵列为基础的甲基化调查的老年人大脑的日期。我们的开源数据集可以作为未来研究的大脑区域参考面板,并帮助推进衰老和神经退行性疾病的研究。在线版本包含补充材料,可通过10.1186/s40478-022-01470-0获得。
Alzheimer’s disease (AD) is the most common cause of dementia with advancing age as its strongest risk factor. AD neuropathologic change (ADNC) is known to be associated with numerous DNA methylation changes in the human brain, but the oldest old (> 90 years) have so far been underrepresented in epigenetic studies of ADNC. Our study participants were individuals aged over 90 years (n = 47) from The 90+ Study. We analyzed DNA methylation from bulk samples in eight precisely dissected regions of the human brain: middle frontal gyrus, cingulate gyrus, entorhinal cortex, dentate gyrus, CA1, substantia nigra, locus coeruleus and cerebellar cortex. We deconvolved our bulk data into cell-type-specific (CTS) signals using computational methods. CTS methylation differences were analyzed across different levels of ADNC. The highest amount of ADNC related methylation differences was found in the dentate gyrus, a region that has so far been underrepresented in large scale multi-omic studies. In neurons of the dentate gyrus, DNA methylation significantly differed with increased burden of amyloid beta (Aβ) plaques at 5897 promoter regions of protein-coding genes. Amongst these, higher Aβ plaque burden was associated with promoter hypomethylation of the Presenilin enhancer 2 (PEN-2) gene, one of the rate limiting genes in the formation of gamma-secretase, a multicomponent complex that is responsible in part for the endoproteolytic cleavage of amyloid precursor protein into Aβ peptides. In addition to novel ADNC related DNA methylation changes, we present the most detailed array-based methylation survey of the old aged human brain to date. Our open-sourced dataset can serve as a brain region reference panel for future studies and help advance research in aging and neurodegenerative diseases. The online version contains supplementary material available at 10.1186/s40478-022-01470-0.
DOI: 10.1038/nbt.1533
发表时间: 2009-04
影响因子: 46.9
作者:
Ball, Madeleine P.;Li, Jin Billy;Gao, Yuan;Lee, Je-Hyuk;LeProust, Emily M.;Park, In-Hyun;Xie, Bin;Daley, George Q.;Church, George M.
通讯作者: Church, George M.
DOI: 10.1038/s41588-022-01024-z
发表时间: 2022-04
期刊: NATURE GENETICS
影响因子: 30.8
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DOI: 10.1093/nar/gku1305
发表时间: 2015-01
影响因子: 14.9
作者:
Illingworth RS;Gruenewald-Schneider U;De Sousa D;Webb S;Merusi C;Kerr AR;James KD;Smith C;Walker R;Andrews R;Bird AP
通讯作者: Bird AP
DOI: 10.1016/j.jalz.2016.04.006
发表时间: 2016-08
期刊: Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子: --
作者:
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通讯作者: Kawas CH
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发表时间: 2006-03-01
影响因子: 4.7
作者:
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通讯作者: Xia, WM