Vimentin Association with Nuclear Grooves in Normal MEF 3T3 Cells

Int J Mol Sci. 2020 Oct 10;21(20):7478. doi: 10.3390/ijms21207478.

Abstract

Vimentin, an intermediate filament protein present in leukocytes, blood vessel endothelial cells, and multiple mesenchymal cells, such as mouse embryonic fibroblasts (MEF 3T3), is crucial for various cellular processes, as well as for maintaining the integrity and durability (stability) of the cell cytoskeleton. Vimentin intermediate filaments (VIFs) adhere tightly to the nucleus and spread to the lamellipodium and tail of the cell, serving as a connector between the nucleus, and the cell's edges, especially in terms of transferring mechanical signals throughout the cell. How these signals are transmitted exactly remains under investigation. In the presented work, we propose that vimentin is involved in that transition by influencing the shape of the nucleus through the formation of nuclear blebs and grooves, as demonstrated by microscopic observations of healthy MEF (3T3) cells. Grooved, or "coffee beans" nuclei, have, to date, been noticed in several healthy cells; however, these structures are especially frequent in cancer cells-they serve as a significant marker for recognition of multiple cancers. We observed 288 MEF3T3 cells cultured on polyhydroxyoctanoate (PHO), polylactide (PLA), and glass, and we identified grooves, coaligned with vimentin fibers in the nuclei of 47% of cells cultured on PHO, 50% of cells on glass, and 59% of cells growing on PLA. We also observed nuclear blebs and associated their occurrence with the type of substrate used for cell culture. We propose that the higher rate of blebs in the nuclei of cells, cultured on PLA, is related to the microenvironmental features of the substrate, pH in particular.

Keywords: cancer; cytoskeleton; fibroblasts; grooved nuclei; intermediate filaments; polyhydroxyoctanoate (PHO); polylactide (PLA); vimentin.

MeSH terms

  • 3T3 Cells
  • Actin Cytoskeleton / metabolism
  • Animals
  • Cell Nucleus / metabolism*
  • Cells, Cultured
  • Fibroblasts / metabolism*
  • Gene Expression
  • Humans
  • Immunohistochemistry
  • Mice
  • Microtubules / metabolism
  • Protein Binding
  • Protein Transport
  • Vimentin / genetics
  • Vimentin / metabolism*

Substances

  • Vimentin