Departments of Genetics, Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Cell and Developmental Biology, The Alexander Silberman Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Mol Biol Cell. 2020 Aug 1;31(17):1943-1950. doi: 10.1091/mbc.E20-01-0085. Epub 2020 Jun 17.
Nuclei within cells are constantly subjected to compressive, tensile, and shear forces, which regulate nucleoskeletal and cytoskeletal remodeling, activate signaling pathways, and direct cell-fate decisions. Multiple rheological methods have been adapted for characterizing the response to applied forces of isolated nuclei and nuclei within intact cells. However, in vitro measurements fail to capture the viscoelastic modulation of nuclear stress-strain relationships by the physiological tethering to the surrounding cytoskeleton, extracellular matrix and cells, and tissue-level architectures. Using an equiaxial stretching apparatus, we applied a step stress and measured nucleus deformation dynamics within living nematodes. Nuclei deformed nonmonotonically under constant load. Nonmonotonic deformation was conserved across tissues and robust to nucleoskeletal and cytoskeletal perturbations, but it required intact linker of nucleoskeleton and cytoskeleton complex attachments. The transition from creep to strain recovery fits a tensile-compressive linear viscoelastic model that is indicative of nucleoskeletal-cytoskeletal decoupling under high load. Ce-lamin () knockdown softened the nucleus, whereas nematode aging stiffened the nucleus and decreased deformation recovery rate. Recovery lasted minutes rather than seconds due to physiological damping of the released mechanical energy, thus protecting nuclear integrity and preventing chromatin damage.
细胞内的核体会不断受到压缩、拉伸和剪切力的作用,这些力调节核骨架和细胞骨架的重塑,激活信号通路,并指导细胞命运的决定。已经有多种流变学方法被用于描述分离核和完整细胞内核对施加力的响应。然而,体外测量无法捕捉到核的粘弹性调制,而这种调制是由与周围细胞骨架、细胞外基质和组织水平结构的生理连接引起的。我们使用等轴拉伸装置,在活线虫中施加阶跃应力,并测量细胞核的变形动力学。在恒载下,细胞核的变形是非单调的。非单调变形在组织间是保守的,并且对核骨架和细胞骨架的扰动具有鲁棒性,但它需要完整的核骨架-细胞骨架连接复合物的附着。从蠕变到应变恢复的转变符合拉伸-压缩线性粘弹性模型,表明在高负荷下核骨架-细胞骨架的解耦。Ce-层粘连蛋白()的敲低使核变软,而线虫的衰老使核变硬,并降低了变形恢复速率。由于释放的机械能的生理阻尼,恢复持续数分钟而不是数秒,从而保护了核的完整性并防止了染色质损伤。