Niels Bohr Institute, University of Copenhagen, 2100 Copenhagen, Denmark.
The Novo Nordisk Foundation Center for Stem Cell Biology, 2200 Copenhagen, Denmark.
Cells. 2021 Oct 23;10(11):2859. doi: 10.3390/cells10112859.
The cellular cytoskeleton provides the cell with a mechanical rigidity that allows mechanical interaction between cells and the extracellular environment. The actin structure plays a key role in mechanical events such as motility or the establishment of cell polarity. From the earliest stages of development, as represented by the ex vivo expansion of naïve embryonic stem cells (ESCs), the critical mechanical role of the actin structure is becoming recognized as a vital cue for correct segregation and lineage control of cells and as a regulatory structure that controls several transcription factors. Naïve ESCs have a characteristic morphology, and the ultrastructure that underlies this condition remains to be further investigated. Here, we investigate the 3D actin cytoskeleton of naïve mouse ESCs using super-resolution optical reconstruction microscopy (STORM). We investigate the morphological, cytoskeletal, and mechanical changes in cells cultured in 2i or Serum/LIF media reflecting, respectively, a homogeneous preimplantation cell state and a state that is closer to embarking on differentiation. STORM imaging showed that the peripheral actin structure undergoes a dramatic change between the two culturing conditions. We also detected micro-rheological differences in the cell periphery between the cells cultured in these two media correlating well with the observed nano-architecture of the ESCs in the two different culture conditions. These results pave the way for linking physical properties and cytoskeletal architecture to cell morphology during early development.
细胞骨架为细胞提供机械刚性,允许细胞与细胞外环境之间进行机械相互作用。肌动蛋白结构在运动或细胞极性建立等机械事件中发挥关键作用。从早期发育阶段(如幼稚胚胎干细胞 (ESC) 的体外扩增)开始,肌动蛋白结构的关键机械作用被认为是细胞正确分离和谱系控制的重要线索,也是控制几个转录因子的调节结构。幼稚 ESC 具有独特的形态,其基础的超微结构仍有待进一步研究。在这里,我们使用超高分辨率光学重构显微镜 (STORM) 研究了幼稚小鼠 ESC 的 3D 肌动蛋白细胞骨架。我们研究了在 2i 或血清/LIF 培养基中培养的细胞的形态、细胞骨架和机械变化,分别反映了同质的植入前细胞状态和更接近开始分化的状态。STORM 成像显示,在两种培养条件下,外周肌动蛋白结构发生了剧烈变化。我们还检测到在这两种培养基中培养的细胞之间细胞边缘的微流变学差异,这与在两种不同培养条件下观察到的 ESC 的纳米结构很好地相关。这些结果为在早期发育过程中连接物理特性和细胞骨架结构与细胞形态铺平了道路。