Rat livers were perfused with 0.5% Triton X-100 for 30 to 60 min and studied by scanning electron microscope. Three-dimensional filamentous networks were visualized in the cytoplasm of hepatocytes in situ. Branching and end-to-side contacts of intermediate filaments, and intermediate filaments which
Transmission electron microscopy of the cytoskeleton of migratory and invasive cells
β Scribed by McGarvey, Terence ;Persky, Bruce
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1989
- Tongue
- English
- Weight
- 310 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0741-0581
No coin nor oath required. For personal study only.
β¦ Synopsis
INTRODUCTION.
The recent development of Transwell cell culture chamber inserts (Costar Co., Cambridge, MA; cat. nos. 3421 & 3422) permits analysis of cellular migration and invasion. Transwell inserts contain a porous polycarbonate membrane and fit into 6 and 24 well cluster plates. Although cellular migration and invasion through polycarbonate membranes have been quantitated by routine LM, SEM and radiolabel techniques, few reports have focused on the cytoskeleton of cells in the process of moving through pores. This communication reports a methodology to evaluate the cytoskeleton of both migratory and invasive tumor cells within 5 and 8 um diameter pore Transwell membranes.
π SIMILAR VOLUMES
## Abstract Examination of whole mount cells in the transmission electron microscope has been useful in studies of cellular architecture. The common technique is to grow cells directly on formvarβcoated, gold grids for direct observation through a cell. We report a technique for obtaining whole mou
## Abstract Primordial germ cells (PGCs) from the dorsal side of midgut endoderm and from within the dorsal mesentery were examined by transmission and scanning electron microscopy. During migration of these cells, lamellipodia and filopodia, develop in a polarized pattern. Large amounts of extrace