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Measuring nucleus mechanics within a living multicellular organism: Physical decoupling and attenuated recovery rate are physiological protective mechanisms of the cell nucleus under high mechanical load

机译:测量活性多细胞生物内的核力学:物理去耦和减毒回收率是在高机械载荷下细胞核的生理保护机制

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摘要

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 Caenorhabditis elegans 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 (lmn-1) 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.
机译:细胞内的核常常经常进行压缩,拉伸和剪切力,其调节核骨骼和细胞骨骼重塑,激活信号通路和直接细胞命运决策。已经调整了多种流变方法,用于表征对完整细胞内分离核和核的施加力的响应。然而,在体外测量不能通过生理系列到周围的细胞骨架,细胞外基质和细胞和组织级架构来捕获核应激关系的粘弹性调节。使用等轴拉伸装置,我们在生活中施加了阶梯应力和测量的核心变形动态,生活中的秀丽隐杆线虫线虫内部。细胞核在恒定载荷下非语文学变形。非单调变形在组织中保守并鲁棒到核骨骼和细胞骨骼扰动,但它需要完整的核心骨骼和细胞骨架复合物附着的接头。从蠕变到应变恢复的过渡适用于拉伸压缩线性粘弹性模型,其指示在高负荷下的核骨骼细胞骨骼去耦。 CE-LAMIN(LMN-1)敲低软化核,而NEMATODE老化加强核并降低变形回收率。恢复持续的分钟而不是秒,因为释放的机械能的生理阻尼,从而保护核完整性并防止染色质损伤。

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