School of Medicine, Life and Health Sciences Research Institute (ICVS), University of Minho, Braga, Portugal.
ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Cell Prolif. 2021 Jul;54(7):e13027. doi: 10.1111/cpr.13027. Epub 2021 May 14.
The area of the subventricular zone (SVZ) in the adult brain exhibits the highest number of proliferative cells, which, together with the olfactory bulb (OB), maintains constant brain plasticity through the generation, migration and integration of newly born neurons. Despite Tau and its malfunction is increasingly related to deficits of adult hippocampal neurogenesis and brain plasticity under pathological conditions [e.g. in Alzheimer's disease (AD)], it remains unknown whether Tau plays a role in the neurogenic process of the SVZ and OB system under conditions of chronic stress, a well-known sculptor of brain and risk factor for AD.
Different types of newly born cells in SVZ and OB were analysed in animals that lack Tau gene (Tau-KO) and their wild-type littermates (WT) under control or chronic stress conditions.
We demonstrate that chronic stress reduced the number of proliferating cells and neuroblasts in the SVZ leading to decreased number of newborn neurons in the OB of adult WT, but not Tau-KO, mice. Interestingly, while stress-evoked changes were not detected in OB granular cell layer, Tau-KO exhibited increased number of mature neurons in this layer indicating altered neuronal migration due to Tau loss.
Our findings suggest the critical involvement of Tau in the neurogenesis suppression of SVZ and OB neurogenic niche under stressful conditions highlighting the role of Tau protein as an essential regulator of stress-driven plasticity deficits.
成年大脑的侧脑室下区 (SVZ) 具有数量最多的增殖细胞,与嗅球 (OB) 一起,通过新生神经元的产生、迁移和整合,维持大脑的持续可塑性。尽管 Tau 及其功能障碍与病理性条件下成年海马神经发生和大脑可塑性的缺陷密切相关[例如在阿尔茨海默病 (AD) 中],但仍不清楚 Tau 是否在 SVZ 和 OB 系统的神经发生过程中发挥作用在慢性应激的条件下,慢性应激是大脑的一个重要塑造者,也是 AD 的一个风险因素。
在缺乏 Tau 基因 (Tau-KO) 的动物和它们的野生型同窝仔鼠 (WT) 中,分析了 SVZ 和 OB 中的不同类型的新生细胞,分别在对照或慢性应激条件下。
我们证明慢性应激减少了 SVZ 中增殖细胞和神经前体细胞的数量,导致成年 WT 小鼠 OB 中新生神经元的数量减少,但 Tau-KO 小鼠则没有。有趣的是,虽然在 OB 的颗粒细胞层中没有检测到应激引起的变化,但 Tau-KO 显示该层中成熟神经元的数量增加,表明由于 Tau 缺失导致神经元迁移改变。
我们的研究结果表明 Tau 在内侧脑室下区 (SVZ) 和 OB 神经发生龛的神经发生抑制中具有关键作用,强调了 Tau 蛋白作为应激驱动的可塑性缺陷的重要调节因子的作用。