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Effects of Alcohol Abuse on Proliferating Cells Stem/Progenitor Cells and Immature Neurons in the Adult Human Hippocampus

机译:酗酒对成年人类海马细胞增殖干/祖细胞和未成熟神经元的影响

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摘要

In animal studies, impaired adult hippocampal neurogenesis is associated with behavioral pathologies including addiction to alcohol. We hypothesize that alcohol abuse may have a detrimental effect on the neurogenic pool of the dentate gyrus in the human hippocampus. In this study we investigate whether alcohol abuse affects the number of proliferating cells, stem/progenitor cells, and immature neurons in samples from postmortem human hippocampus. The specimens were isolated from deceased donors with an on-going alcohol abuse, and from controls with no alcohol overconsumption. Mid-hippocampal sections were immunostained for Ki67, a marker for cell proliferation, Sox2, a stem/progenitor cell marker, and DCX, a marker for immature neurons. Immunoreactivity was counted in alcoholic subjects and compared with controls. Counting was performed in the three layers of dentate gyrus: the subgranular zone, the granular cell layer, and the molecular layer. Our data showed reduced numbers of all three markers in the dentate gyrus in subjects with an on-going alcohol abuse. This reduction was most prominent in the subgranular zone, and uniformly distributed across the distances from the granular cell layer. Furthermore, alcohol abusers showed a more pronounced reduction of Sox2-IR cells than DCX-IR cells, suggesting that alcohol primarily causes a depletion of the stem/progenitor cell pool and that immature neurons are secondarily affected. These results are in agreement with observations of impaired adult hippocampal neurogenesis in animal studies and lend further support for the association between hippocampal dysfunction and alcohol abuse.
机译:在动物研究中,成年海马神经发生受损与包括酒精成瘾在内的行为病理有关。我们假设酗酒可能会对人海马中齿状回的神经源池产生不利影响。在这项研究中,我们调查了酗酒是否会影响死后人类海马样本中增殖细胞,干/祖细胞和未成熟神经元的数量。这些标本是从持续饮酒的死者捐赠者和没有过量饮酒的对照组中分离出来的。对海马中部进行免疫染色,以检测Ki67(细胞增殖的标志物),Sox2(干/祖细胞标志物)和DCX(未成熟神经元的标志物)。对酒精受试者的免疫反应性进行计数,并与对照组进行比较。在齿状回的三层中进行计数:亚颗粒区,颗粒细胞层和分子层。我们的数据显示,在持续酗酒的受试者中,齿状回中所有三个标记物的数量均减少。这种减少在亚颗粒区最为明显,并且在与颗粒细胞层的距离上均匀分布。此外,酗酒者显示出Sox2-IR细胞比DCX-IR细胞更明显地减少,这表明酒精主要导致干/祖细胞池的消耗,而未成熟的神经元则受到了进一步的影响。这些结果与动物研究中成人海马神经发生受损的观察结果一致,并进一步支持了海马功能障碍与酗酒之间的关联。

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