Department of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, Minamikogushi 1-1-1, Ube, 755-8505, Japan.
Laboratory of Molecular Developmental Biology, Faculty of Biology-Oriented Science and Technology, Kindai University, Wakayama, 649-6493, Japan.
Commun Biol. 2024 Jul 11;7(1):830. doi: 10.1038/s42003-024-06492-z.
Decidualization of the human endometrium is critical for establishing pregnancy and is entailed by differentiation of endometrial stromal cells (ESCs) into decidual cells. During decidualization, the actin cytoskeleton is dynamically reorganized for the ESCs' morphological and functional changes. Although actin dynamically alters its polymerized state upon external stimuli not only in the cytoplasm, but also in the nucleus, nuclear actin dynamics during decidualization have not been elucidated. Here, we show that nuclear actin was specifically assembled during decidualization of human ESCs. This decidualization-specific formation of nuclear actin filaments was disassembled following the withdrawal of the decidualization stimulus, suggesting its reversible process. Mechanistically, RNA-seq analyses revealed that the forced disassembly of nuclear actin resulted in the suppression of decidualization, accompanied with the abnormal upregulation of cell proliferation genes, leading to incomplete cell cycle arrest. CCAAT/enhancer-binding protein beta (C/EBPβ), an important regulator for decidualization, was responsible for downregulation of the nuclear actin exporter, thus accelerating nuclear actin accumulation and its assembly for decidualization. Taken together, we demonstrate that decidualization-specific nuclear actin assembly induces cell cycle arrest for establishing the decidualized state of ESCs. We propose that not only the cytoplasmic actin, but also nuclear actin dynamics profoundly affect decidualization process in humans for ensuring pregnancy.
人子宫内膜的蜕膜化对于建立妊娠至关重要,它涉及到子宫内膜基质细胞(ESCs)向蜕膜细胞的分化。在蜕膜化过程中,肌动蛋白细胞骨架为 ESCs 的形态和功能变化进行动态重排。尽管肌动蛋白不仅在细胞质中,而且在细胞核中,都会在外来刺激下动态改变其聚合状态,但在蜕膜化过程中细胞核内肌动蛋白的动力学尚未得到阐明。在这里,我们显示细胞核内肌动蛋白在人 ESC 的蜕膜化过程中被特异性组装。这种蜕膜化特异性核肌动蛋白丝的组装在蜕膜化刺激的撤回后被拆卸,表明其是一个可逆的过程。从机制上讲,RNA-seq 分析显示,核肌动蛋白的强制拆卸导致蜕膜化的抑制,伴随着细胞增殖基因的异常上调,导致不完全的细胞周期停滞。CCAAT/增强子结合蛋白β(C/EBPβ)是蜕膜化的重要调节因子,负责下调核肌动蛋白输出蛋白,从而加速核肌动蛋白的积累及其用于蜕膜化的组装。总之,我们证明了蜕膜化特异性核肌动蛋白组装诱导细胞周期停滞,从而建立 ESCs 的蜕膜化状态。我们提出,不仅细胞质肌动蛋白,而且细胞核内肌动蛋白动力学都深刻地影响了人类的蜕膜化过程,以确保妊娠。