Universally Conserved Relationships between Nuclear Shape and Cytoplasmic Mechanical Properties in Human Stem Cells

Sci Rep. 2016 Mar 15:6:23047. doi: 10.1038/srep23047.

Abstract

The ability of cells to proliferate, differentiate, transduce extracellular signals and assemble tissues involves structural connections between nucleus and cytoskeleton. Yet, how the mechanics of these connections vary inside stem cells is not fully understood. To address those questions, we combined two-dimensional particle-tracking microrheology and morphological measures using variable reduction techniques to measure whether cytoplasmic mechanics allow for discrimination between different human adherent stem cell types and across different culture conditions. Here we show that nuclear shape is a quantifiable discriminant of mechanical properties in the perinuclear cytoskeleton (pnCSK) of various stem cell types. Also, we find the pnCSK is a region with different mechanical properties than elsewhere in the cytoskeleton, with heterogeneously distributed locations exhibiting subdiffusive features, and which obeys physical relations conserved among various stem cell types. Finally, we offer a prospective basis to discriminate between stem cell types by coupling perinuclear mechanical properties to nuclear shape.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actins / metabolism
  • Adipose Tissue / cytology
  • Analysis of Variance
  • Cell Adhesion / physiology
  • Cell Line
  • Cell Nucleus / metabolism
  • Cell Nucleus / physiology*
  • Cells, Cultured
  • Cytoplasm / metabolism
  • Cytoplasm / physiology*
  • Cytoskeleton / metabolism
  • Cytoskeleton / physiology
  • Humans
  • Induced Pluripotent Stem Cells / cytology
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / physiology
  • Mechanotransduction, Cellular / physiology*
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism
  • Mesenchymal Stem Cells / physiology
  • Microscopy, Confocal
  • Prospective Studies
  • Rheology / methods
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Stem Cells / physiology*
  • Time-Lapse Imaging / methods

Substances

  • Actins