Cytoskeleton Architecture of C6 Rat Glioma Cell Subclones Whole Mount Electron Microscopy and Immunogold Labeling

Authors

Wolfgang Bohn, Heinrich-Pette-Institut, Germany
Dörte Etzrodt, Heinrich-Pette-Institut, Germany
Roland Foisner, University of Vienna, Austria
Gerhard Wiche, University of Vienna, Austria
Peter Traub, Max-Planck-Institute of Cell Biology, Germany

Abstract

Whole mount electron microscopy of extracted cells combined with immunogold labeling techniques can be used to characterize the cytoskeletal architecture of cultured cells. As shown with subclones of the C6 rat glioma cell line, heavy metal shadowing was suitable for getting basic information concerning the arrangement of the various filament types within the networks. Pure carbon shadowing combined with immunogold double labeling proved to be optimal to identify linkages between filaments, to localize filament associated proteins and to follow the arrangement of filaments in dense arrays such as lamellipodiae and cell margins. Thin connecting filaments which interact with actin as well as with vimentin filaments and can be labeled with antibodies to the intermediate filament associated protein plectin may play a major role in the structural organization of the cytoskeleton of these cells.

Recommended Citation

Bohn, Wolfgang; Etzrodt, Dörte; Foisner, Roland; Wiche, Gerhard; and Traub, Peter (1996) "Cytoskeleton Architecture of C6 Rat Glioma Cell Subclones Whole Mount Electron Microscopy and Immunogold Labeling," Scanning Microscopy: Vol. 1996: No. 10, Article 23.
Available at: https://digitalcommons.usu.edu/microscopy/vol1996/iss10/23