AFM visualization of cortical filaments/network under cell-bound membrane vesicles

Biochim Biophys Acta. 2015 Oct;1848(10 Pt A):2225-32. doi: 10.1016/j.bbamem.2015.06.025. Epub 2015 Jul 2.

Abstract

While circulating/plasma membrane vesicles have been extensively characterized, due to the lack of effective methods cell-bound membrane vesicles are poorly understood including their shape and correlation with the intracellular cytoskeleton. In this study, we focused on cell-bound membrane vesicles and individual vesicle-derived pits on endothelial cells by using confocal microscopy and atomic force microscopy (AFM). For the first time, we found that cell-bound membrane vesicles are hemisphere-shaped and that the actin cortical filaments/network lies at the cytosolic opening of a vesicle instead of being closely attached to the inner side of the vesicle membrane. This structure of cell-bound membrane vesicles may be beneficial to their movement in, or release from, the plasma membrane of cells due to less membrane-cytoskeleton coupling to be broken therefore probably minimizing energy consumption and time usage. Further study indicates that TNF-α activation induced a significant increase in average number/size of cell-bound vesicles and the local disruption of the actin network at the cytosolic opening of cell-bound vesicles.

Keywords: Atomic force microscopy (AFM); Cortical filaments/network; Endothelial cells; Membrane vesicles; TNF-α; Vesicle-derived pits.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / drug effects
  • Actin Cytoskeleton / ultrastructure*
  • Cell Membrane / drug effects
  • Cell Membrane / ultrastructure*
  • Cells, Cultured
  • Endothelial Cells / drug effects
  • Endothelial Cells / ultrastructure*
  • Humans
  • Membrane Fluidity / drug effects
  • Microscopy, Atomic Force / methods*
  • Transport Vesicles / drug effects
  • Transport Vesicles / ultrastructure*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Tumor Necrosis Factor-alpha