Improved method for visualizing coated pits, microfilaments, and microtubules in cryofixed and freeze-substituted plant cells

J Electron Microsc (Tokyo). 2002;51(2):133-6. doi: 10.1093/jmicro/51.2.133.

Abstract

We have optimized the conditions for visualizing microfilaments, microtubules, and coated pits in the cortical cytoplasm of high-pressure frozen and freeze-substituted plant cells, in both tobacco root tips and onion cotyledons, individual microfilaments and the supramolecular structure of coated pits can be seen clearly in freeze-substituted samples treated with OsO4 at 40 degrees C followed by 5% uranyl acetate. Treatment with uranyl acetate alone resulted in poorly stained cytoplasmic organelles, whereas microfilaments were difficult to discern in specimen treated with OsO4 alone. The combination of a 40 degrees C OsO4 staining step followed by staining with uranyl acetate at 4 degrees C should prove useful for more detailed plant cytoskeletal/membrane studies in the future.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actin Cytoskeleton / ultrastructure*
  • Coated Pits, Cell-Membrane / ultrastructure*
  • Cotyledon / ultrastructure
  • Cryopreservation
  • Freeze Substitution
  • Microscopy, Electron / methods
  • Microtubules / ultrastructure*
  • Nicotiana / ultrastructure*
  • Onions / ultrastructure*
  • Organometallic Compounds
  • Osmium Tetroxide
  • Plant Roots / ultrastructure
  • Staining and Labeling / methods

Substances

  • Organometallic Compounds
  • uranyl acetate
  • Osmium Tetroxide