Abstract

ABSTRACTMigrating cells have to cross many physical barriers and confined in 3D environments. The surrounding environment promotes mechano- and biological signals that orchestrate cellular changes, such as cytoskeletal and adhesion rearrangements and proteolytic digestion. Recent studies provide new insights into how the nucleus must alter its shape, localization and mechanical properties in order to promote nuclear deformability, chromatin compaction and gene reprogramming. It is known that the chromatin structure contributes directly to genomic and non-genomic functions, such as gene transcription and the physical properties of the nucleus. Here, we appraise paradigms and novel insights regarding the functional role of chromatin during nuclear deformation. In so doing, we review how constraint and mechanical conditions influence the structure, localization and chromatin decompaction. Finally, we highlight the emerging roles of mechanogenomics and the molecular basis of nucleoskeletal components, which open unexplored territory to understand how cells regulate their chromatin and modify the nucleus.

Highlights

  • Migrating cells have to cross many physical barriers and confined in 3D environments

  • The structure of chromatin is regulated by epigenetic changes, which are defined as non-genomic modifications that alter chromatin compaction and configuration [14]

  • Others previously showed that chromatin condensation is associated with lower nuclear deformability in mesenchymal stem cells (MSCs), which reinforces the idea that chromatin controls a different biomechanical response than lamins [10,19]

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Summary

Introduction

Migrating cells have to cross many physical barriers and confined in 3D environments. KEYWORDS Epigenetics; mechanogenomics; chromatin; cell migration; nuclear mechanics We will review recent studies that describe the influence of chromatin on the mechanical properties of the nucleus.

Results
Conclusion

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