Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL; Department of Developmental and Stem Cell Biology, Institut Pasteur, Université de Paris Cité, CNRS.
Center for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS, INSERM, Université PSL.
J Vis Exp. 2024 Jan 12(203). doi: 10.3791/65976.
A major challenge in understanding the causes of female infertility is to elucidate mechanisms governing the development of female germ cells, named oocytes. Their development is marked by cell growth and subsequent divisions, two critical phases that prepare the oocyte for fusion with sperm to initiate embryogenesis. During growth, oocytes reorganize their cytoplasm to position the nucleus at the cell center, an event predictive of successful oocyte development in mice and humans and, thus, their embryogenic potential. In mouse oocytes, this cytoplasmic reorganization was shown to be driven by the cytoskeleton, the activity of which generates mechanical forces that agitate, reposition, and penetrate the nucleus. Consequently, this cytoplasmic-to-nucleoplasmic force transmission tunes the dynamics of nuclear RNA-processing organelles known as biomolecular condensates. This protocol provides an experimental framework to document, with high temporal resolution, the impact of the cytoskeleton on the nucleus across spatial scales in mouse oocytes. It details the imaging and image analysis steps and tools necessary to evaluate i) cytoskeletal activity in the oocyte cytoplasm, ii) cytoskeleton-based agitation of the oocyte nucleus, and iii) its effects on biomolecular condensate dynamics in the oocyte nucleoplasm. Beyond oocyte biology, the methods elaborated here can be adapted for use in somatic cells to similarly address cytoskeleton-based tuning of nuclear dynamics across scales.
理解女性不孕原因的一个主要挑战是阐明调控雌性生殖细胞(即卵母细胞)发育的机制。卵母细胞的发育过程以细胞生长和随后的分裂为标志,这两个关键阶段为卵母细胞与精子融合并启动胚胎发生做好了准备。在生长过程中,卵母细胞会重新组织细胞质,将细胞核定位在细胞中心,这一事件可以预测小鼠和人类卵母细胞的发育是否成功,从而预测其胚胎发生的潜力。在小鼠卵母细胞中,这种细胞质的重新组织被证明是由细胞骨架驱动的,细胞骨架的活动产生机械力,从而搅动、重新定位和穿透细胞核。因此,这种细胞质到核质的力传递可以调节核内 RNA 处理细胞器(称为生物分子凝聚物)的动力学。本方案提供了一个实验框架,可在高时间分辨率下记录细胞骨架对小鼠卵母细胞中核的空间尺度的影响。它详细说明了成像和图像分析步骤以及必要的工具,以评估 i)卵母细胞质中的细胞骨架活性,ii)卵母细胞核基于细胞骨架的搅动,以及 iii)其对卵母细胞核质中生物分子凝聚物动力学的影响。除了卵母细胞生物学之外,这里阐述的方法可以适应用于体细胞,以类似的方式解决核动力学的基于细胞骨架的跨尺度调节。