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Journal ArticleDOI

Mechanisms and functions of nuclear envelope remodelling

Rosemarie Ungricht, +1 more
- 01 Apr 2017 - 
- Vol. 18, Iss: 4, pp 229-245
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TLDR
The nuclear envelope is shown to be a dynamic and highly adaptable boundary that changes composition during differentiation, deforms in response to mechanical challenges, can be repaired upon rupture and even rapidly disassembles and reforms during open mitosis.
Abstract
As a compartment border, the nuclear envelope (NE) needs to serve as both a protective membrane shell for the genome and a versatile communication interface between the nucleus and the cytoplasm. Despite its important structural role in sheltering the genome, the NE is a dynamic and highly adaptable boundary that changes composition during differentiation, deforms in response to mechanical challenges, can be repaired upon rupture and even rapidly disassembles and reforms during open mitosis. NE remodelling is fundamentally involved in cell growth, division and differentiation, and if perturbed can lead to devastating diseases such as muscular dystrophies or premature ageing.

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Citations
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Emerging roles for the nucleus during neutrophil signal relay and NETosis.

TL;DR: This review presents emerging evidence suggesting that a unique, ambiguous cell-cycle state is critical for NETosis and migration, and discusses how the mechanisms underlying migration and NETosis are evolutionarily conserved.
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Mechanisms of allelic and clinical heterogeneity of lamin A/C phenotypes.

TL;DR: Experimental support has been provided for different models of cellular pathogenesis in nuclear envelope diseases, including changes in heterochromatin formation at the nuclear membrane (epigenomics), changes in the timing of steps during terminal differentiation of cells, and structural abnormalities of the nuclear membranes.
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Three‐Dimensional Visualization of Subcellular Dynamics of Cancer Cell Destruction on Therapeutic Nanodrug Treatment

TL;DR: The deleterious repercussions of the therapeutic gold nanocages (TANs) on the subcellular organelles of MCF7 cells are studied and a previously unknown systemic degradation process of mitochondria and the structure of autolysosome is revealed.
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Physiochemical Effects of Nanoparticles on Cell Nuclear Complex Pore Transport: A Coarse-Grained Computational Model.

TL;DR: This work provides a systematic understanding for nuclear uptake of nanoparticles, viruses, and bacteria, and opens up a controllable design strategy for manipulating nanoparticle-nucleus interaction, with numerous applications in medicine, bio-imaging, and bio-sensing.
Journal ArticleDOI

Toward an Axial Nanoscale Ruler for Fluorescence Microscopy.

TL;DR: Fluorescence lifetime imaging can be used as an axial ruler with nanometer precision and metal-enhanced energy transfer is applied, recently extended to multicolor distance measurements and applied to study the topography of the nuclear membrane.
References
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Journal ArticleDOI

Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions

TL;DR: A high-resolution map of the interaction sites of the entire genome with NL components in human fibroblasts is constructed and demonstrates that the human genome is divided into large, discrete domains that are units of chromosome organization within the nucleus.
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Nuclear lamin-A Scales With Tissue Stiffness and Enhances Matrix-Directed Differentiation

TL;DR: In this article, proteomics analyses revealed that levels of the nucleoskeletal protein lamin-A scaled with tissue elasticity, as did levels of collagens in the extracellular matrix that determine E.
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