Brigham and Women's Hospital/Harvard Medical School, Cambridge, Massachusetts, USA.
Compr Physiol. 2011 Apr;1(2):783-807. doi: 10.1002/cphy.c100038.
The nucleus is the distinguishing feature of eukaryotic cells. Until recently, it was often considered simply as a unique compartment containing the genetic information of the cell and associated machinery, without much attention to its structure and mechanical properties. This article provides compelling examples that illustrate how specific nuclear structures are associated with important cellular functions, and how defects in nuclear mechanics can cause a multitude of human diseases. During differentiation, embryonic stem cells modify their nuclear envelope composition and chromatin structure, resulting in stiffer nuclei that reflect decreased transcriptional plasticity. In contrast, neutrophils have evolved characteristic lobulated nuclei that increase their physical plasticity, enabling passage through narrow tissue spaces in their response to inflammation. Research on diverse cell types further demonstrates how induced nuclear deformations during cellular compression or stretch can modulate cellular function. Pathological examples of disturbed nuclear mechanics include the many diseases caused by mutations in the nuclear envelope proteins lamin A/C and associated proteins, as well as cancer cells that are often characterized by abnormal nuclear morphology. In this article, we will focus on determining the functional relationship between nuclear mechanics and cellular (dys-)function, describing the molecular changes associated with physiological and pathological examples, the resulting defects in nuclear mechanics, and the effects on cellular function. New insights into the close relationship between nuclear mechanics and cellular organization and function will yield a better understanding of normal biology and will offer new clues into therapeutic approaches to the various diseases associated with defective nuclear mechanics.
细胞核是真核细胞的显著特征。直到最近,人们通常认为细胞核仅仅是一个包含细胞遗传信息和相关机制的独特隔室,而很少关注其结构和力学性质。本文提供了令人信服的例子,说明特定的核结构如何与重要的细胞功能相关联,以及核力学的缺陷如何导致多种人类疾病。在分化过程中,胚胎干细胞改变其核膜组成和染色质结构,导致核变硬,反映出转录可塑性降低。相比之下,中性粒细胞已经进化出特征性的分叶核,增加了物理可塑性,使其能够在响应炎症时通过狭窄的组织间隙。对不同细胞类型的研究进一步表明,细胞在受到压缩或拉伸时诱导的核变形如何调节细胞功能。核力学紊乱的病理实例包括许多由核膜蛋白 lamin A/C 和相关蛋白突变引起的疾病,以及通常具有异常核形态的癌细胞。在本文中,我们将重点研究核力学与细胞(功能)障碍之间的功能关系,描述与生理和病理实例相关的分子变化、核力学的相应缺陷以及对细胞功能的影响。对核力学与细胞组织和功能之间密切关系的新认识将更好地理解正常生物学,并为与核力学缺陷相关的各种疾病的治疗方法提供新的线索。