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急性膳食蛋氨酸限制会引发新皮质中的细胞周期停滞和可逆性生长缺陷。

Acute dietary methionine restriction triggers cell cycle arrest and reversible growth defects in the neocortex.

作者信息

Saha Sulov, Debacq Clémence, Audouard Christophe, Jungas Thomas, Dupré Pierrick, Mohamad-Ali Fawal, Chapat Clément, Michaud Henri-Alexandre, Le Cam Laurent, Lacroix Matthieu, Ohayon David, Davy Alice

机构信息

Molecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.

Institut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Université de Montpellier, Institut Régional du Cancer de Montpellier (ICM), 34298 Montpellier, France.

出版信息

iScience. 2025 May 21;28(6):112705. doi: 10.1016/j.isci.2025.112705. eCollection 2025 Jun 20.

Abstract

Methionine is indispensable for cell proliferation, stem cell maintenance, and epigenetic regulation, three processes that are central to embryonic development. Here, we assessed the consequences of short-term dietary methionine restriction (MR) on mouse embryonic organ growth. In comparison with growth of the liver and heart which was unaffected, MR for 5 days led to a severe reduction in neuronal production and neocortex growth. Progenitor cohort labeling revealed a time-dependent sensitivity to MR and cell cycle analysis indicated that progenitors are stalled in S/G2 phases following MR. Unexpectedly, neuronal production was completely rescued at birth when switching the dam back to control diet, uncovering a mechanism of catch-up growth. We used imaging mass cytometry to probe metabolic and epigenetic markers in neural progenitors following MR and during catch-up growth. Altogether, our data uncover a reversible state of quiescence in S/G2 which is metabolically distinct from G0 quiescence and associated with efficient catch-up growth of the neocortex.

摘要

甲硫氨酸对于细胞增殖、干细胞维持和表观遗传调控不可或缺,而这三个过程是胚胎发育的核心。在此,我们评估了短期饮食中甲硫氨酸限制(MR)对小鼠胚胎器官生长的影响。与未受影响的肝脏和心脏生长相比,5天的MR导致神经元生成和新皮质生长严重减少。祖细胞群体标记显示对MR存在时间依赖性敏感性,细胞周期分析表明祖细胞在MR后停滞于S/G2期。出乎意料的是,当将母鼠换回对照饮食时,出生时神经元生成完全恢复,揭示了一种追赶生长机制。我们使用成像质谱流式细胞术来探测MR后及追赶生长期间神经祖细胞中的代谢和表观遗传标记。总之,我们的数据揭示了S/G2期一种可逆的静止状态,其在代谢上不同于G0期静止,且与新皮质的有效追赶生长相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f192/12167773/2aac8e23f477/fx1.jpg

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