海马神经发生的转录组分析综述,重点是成体齿状回干细胞。

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-05-30 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1605116
Laura Micheli, Maurizia Caruso, Giorgio D'Andrea, Daniel Volpe, Manuela Ceccarelli, Felice Tirone
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引用次数: 0

摘要

成年哺乳动物的大脑从神经干细胞(NSCs)开始,在两个主要的神经龛中产生新的神经元,海马的齿状回和脑室下区。成人海马神经发生对学习和记忆至关重要,随着年龄的增长而减少。根据小鼠模型的定义,通常处于静止状态的NSCs可发育为增殖祖细胞、成神经细胞以及未成熟和成熟神经元。关于齿状回的NSC自我更新,人们提出了两种观点,一种假设持续的自我更新,即使在老年也有休息和重新激活的周期,另一种则提出了一个短暂的NSC模型。本综述讨论了单细胞RNA测序和克隆研究,揭示了神经源性细胞的发育步骤和自我更新的方式,揭示了NSC异质群体在成年齿状回中的存在,一个长寿命,另一个在早期迅速耗尽。另一个相关的问题是成人神经发生是否发生在人类身上。少数单细胞RNA-seq研究表明,随着神经元成熟时间的延长,干细胞/祖细胞以低频率不断产生新的神经元,导致未成熟颗粒细胞神经元的积累。这表明这些细胞在人类神经发生中起着重要作用,因此在神经发生过程动力学中存在物种间差异。本文通过分析海马神经发生的特定实验环境中神经细胞的发育轨迹和NSCs基因表达谱,以及在缺失或过度表达特定基因以重现神经病变的小鼠模型中,重点关注转录组学研究,这些研究已经面临这些和其他NSC问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Survey of transcriptome analyses of hippocampal neurogenesis with focus on adult dentate gyrus stem cells.

Adult mammalian brains generate new neurons throughout life in two main niches, the dentate gyrus of the hippocampus and the subventricular zone, starting from neural stem cells (NSCs). Adult hippocampal neurogenesis is crucial for learning and memory and decreases during aging. As defined in mouse models, NSCs, which are prevalently quiescent, develop into proliferating progenitor cells, neuroblasts, and immature and mature neurons. Two visions for NSC self-renewal in the dentate gyrus have been proposed, one postulating persistent self-renewal, with cycles of rest and reactivation even in old age, and the other proposing a short-lived NSC model. Single-cell RNA sequencing and clonal studies, discussed in this review, have shed light on the developmental steps of neurogenic cells and the modality of self-renewal, revealing the presence in the adult dentate gyrus of NSC heterogeneous populations, one long-lived and another rapidly depleted at an early age. Another relevant question is whether adult neurogenesis occurs in humans. A few single-cell RNA-seq studies show that new neurons, with prolonged neuronal maturation, are continuously generated at low frequency from stem/progenitor cells, which results in the accumulation of immature granule cell neurons. This suggests an important role of these cells in human neurogenesis and hence interspecies differences in the neurogenic process dynamics. This review is focused on transcriptomic studies that have faced these and other NSC issues by analyzing developmental trajectories of neural cells and NSCs gene expression profiles in specific experimental settings of hippocampal neurogenesis, and also in mouse models with deletion or overexpression of specific genes to reproduce neural pathologies.

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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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