Bingyue Cao, Fengling Luo, Wenwen Zhang, Renwei Luo, Lile Cai, Yongchang Wei, Yanqing Wang, Pan Liu
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引用次数: 0
摘要
近年来,人们从不同方面研究了组蛋白乙酰化在大脑中的作用。然而,组蛋白 H3 乙酰化在人类海马中的解剖分布及其与三重突触回路的潜在相关性尚不清楚。作为表观遗传重塑方式之一,组蛋白的修饰涉及神经元功能和发育的多个方面,也是阿尔茨海默病(AD)发病和发展的关键过程。在我们的研究中,我们比较了 AD 患者和非 AD 患者海马不同区域组蛋白 H3 的乙酰化水平。我们发现,在人类海马的齿状回(DG)、CA4、CA3、CA2、CA1 和下 Toya 区可以检测到组蛋白 H3 乙酰化。海马中乙酰化程度最高的是DG,乙酰化水平沿着三重突触回路逐渐系统地变化。此外,组蛋白乙酰化在AD组和非AD组之间无明显差异。
Anatomical distribution of histone H3 acetylation in human hippocampus
In recent years, the role of histone acetylation in the brain has been studied from different aspects. However, the anatomical distribution of histone H3 acetylation in the human hippocampus and its potential relevance to triple synaptic circuits are unknown. As one of epigenetic remodeling ways, the modification of histones is involved in multiple aspects of neuronal function and development and is a key process in the onset and development of Alzheimer’s disease (AD). In our study, we compared acetylation levels of histone H3 at different regions of the hippocampus in AD and non-AD patients. We found that histone H3 acetylation can be detected in the dentate gyrus (DG), CA4, CA3, CA2, CA1, and lower Toya regions of the human hippocampus. The highest degree of acetylation in the hippocampus is in DG, and the level of acetylation changes gradually and systematically along the triple synaptic circuit. Besides, there were no significant differences in histone acetylation between AD and non-AD groups.