Hostname: page-component-7bb8b95d7b-dvmhs Total loading time: 0 Render date: 2024-10-05T23:11:38.193Z Has data issue: false hasContentIssue false

Immunoelectron Microscopy of Keratinocytes: an Improved Protocol for Flat Embedding of Cultured Cells Using Lowicryl K4M

Published online by Cambridge University Press:  02 July 2020

C. Bauer
Affiliation:
Department of Molecular Genetics and Cell Biology Howard Hughes Medical Institute The University of ChicagoChicago, II60637
V. Vasioukhin
Affiliation:
Department of Molecular Genetics and Cell Biology Howard Hughes Medical Institute The University of ChicagoChicago, II60637
M. Yin
Affiliation:
Department of Molecular Genetics and Cell Biology Howard Hughes Medical Institute The University of ChicagoChicago, II60637
E. Fuchs
Affiliation:
Department of Molecular Genetics and Cell Biology Howard Hughes Medical Institute The University of ChicagoChicago, II60637
Get access

Extract

In cell culture models various and distinct manipulations can be performed in a defined environment. This makes cell cultures very popular for immunohistochemical studies. Such studies are mostly performed at the light microscopic level where fluorescent probes and confocal microscopy provide detailed insights into the distribution and localization of antigens inside cells. In many such cases further studies at the electron microscopic level would give additional information and an often more detailed view. As compared to light microscopy not only is the resolution much higher, but also and even more importantly labeling information is completed with a wealth of cytological details.

This said it is surprising that studies on cell cultures using immunoelectron microscopy are rarely seen. Even more rare are reports in which monolayer cells are fixed and processed in situ without prior trypsinization. Such studies are essential though when cytoarchitecture is of importance or especially when cell-cell adhesion is an issue.

Type
Labeling for Microscopy and Correlative Microscopy
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References:

Vasioukhin, V., Bauer, C., Yin, M. and Fuchs, E.: Directed Actin Polymerization is the Driving Force for Epithelial Cell-Cell Adhesion. Cell, Vol. 100, (2000), 209219CrossRefGoogle ScholarPubMed