在健康和阿尔茨海默病中,神经发生驱动海马形成范围的空间转录改变。

Frontiers in dementia Pub Date : 2025-04-16 eCollection Date: 2025-01-01 DOI:10.3389/frdem.2025.1546433
Zachery D Morrissey, Pavan Kumar, Trongha X Phan, Mark Maienschein-Cline, Alex Leow, Orly Lazarov
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引用次数: 0

摘要

神经发生调节海马形成中神经元和神经胶质的机制尚不清楚。此外,神经发生对阿尔茨海默病(AD)内嗅皮层神经元易感性特征的影响尚不清楚。在这里,我们使用原位测序来研究表达不同水平神经发生的野生型小鼠和家族性AD (FAD)小鼠海马回路中神经元和胶质细胞的空间转录谱。该方法显示,除了齿状回外,神经发生还调节了海马内嗅皮质和CA区域的细胞谱。值得注意的是,FAD小鼠的神经发生增强导致这些大脑区域的神经元和细胞特征部分恢复,类似于野生型小鼠的特征。这种方法为检查健康和阿尔茨海默病患者海马形成中的细胞动力学提供了一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurogenesis drives hippocampal formation-wide spatial transcription alterations in health and Alzheimer's disease.

The mechanism by which neurogenesis regulates the profile of neurons and glia in the hippocampal formation is not known. Further, the effect of neurogenesis on neuronal vulnerability characterizing the entorhinal cortex in Alzheimer's disease (AD) is unknown. Here, we used in situ sequencing to investigate the spatial transcription profile of neurons and glia in the hippocampal circuitry in wild-type mice and in familial AD (FAD) mice expressing varying levels of neurogenesis. This approach revealed that in addition to the dentate gyrus, neurogenesis modulates the cellular profile in the entorhinal cortex and CA regions of the hippocampus. Notably, enhancing neurogenesis in FAD mice led to partial restoration of neuronal and cellular profile in these brain areas, resembling the profile of their wild-type counterparts. This approach provides a platform for the examination of the cellular dynamics in the hippocampal formation in health and in AD.

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