4.8 Article

Image-Based Elastography of Heterochromatin and Euchromatin Domains in the Deforming Cell Nucleus

Journal

SMALL
Volume 17, Issue 5, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202006109

Keywords

chromatin; inverse methods; LINC complex; mechanobiology; nuclear mechanics

Funding

  1. National Science Foundation [CAREER 1349735]
  2. National Institutes of Health [R01 AR063712]

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The study introduces nuclear elastography technology to quantify the relative elasticity of heterochromatin and euchromatin domains within the cell nucleus; experiments reveal rapid changes in relative elasticity between these two regions during cellular deformation; disruption of specific nuclear membrane proteins affects intranuclear elasticity distribution, leading to similarities between heterochromatin and euchromatin.
Chromatin of the eukaryotic cell nucleus comprises microscopically dense heterochromatin and loose euchromatin domains, each with distinct transcriptional ability and roles in cellular mechanotransduction. While recent methods are developed to characterize the mechanics of nucleus, measurement of intranuclear mechanics remains largely unknown. Here, the development of nuclear elastography, which combines microscopic imaging and computational modeling to quantify the relative elasticity of the heterochromatin and euchromatin domains, is described. Using contracting murine embryonic cardiomyocytes, nuclear elastography reveals that the heterochromatin is almost four times stiffer than the euchromatin at peak deformation. The relative elasticity between the two domains changes rapidly during the active deformation of the cardiomyocyte in the normal physiological condition but progresses more slowly in cells cultured in a mechanically stiff environment, although the relative stiffness at peak deformation does not change. Further, it is found that the disruption of the Klarsicht, ANC-1, Syne Homology domain of the Linker of Nucleoskeleton and Cytoskeleton complex compromises the intranuclear elasticity distribution resulting in elastically similar heterochromatin and euchromatin. These results provide insight into the elastography dynamics of heterochromatin and euchromatin domains and provide a noninvasive framework to further investigate the mechanobiological function of subcellular and subnuclear domains limited only by the spatiotemporal resolution of the acquired images.

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