Correlative light and electron microscopy reveals fork-shaped structures at actin entry sites of focal adhesions

Journal Article (2022)
Authors

Karin Legerstee (Erasmus MC)

Josey Sueters (ImPhys/Microscopy Instrumentation & Techniques)

Tsion E. Abraham (Erasmus MC)

J. A. Slotman (Erasmus MC)

G. J. Kremers (Erasmus MC)

Jacob Hoogenboom (ImPhys/Microscopy Instrumentation & Techniques)

A.B. Houtsmuller (Erasmus MC)

Research Group
ImPhys/Microscopy Instrumentation & Techniques
Copyright
© 2022 Karin Legerstee, J. Sueters, Tsion E. Abraham, Johan A. Slotman, Gert Jan Kremers, J.P. Hoogenboom, A.B. Houtsmuller
To reference this document use:
https://doi.org/10.1242/bio.059417
More Info
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Publication Year
2022
Language
English
Copyright
© 2022 Karin Legerstee, J. Sueters, Tsion E. Abraham, Johan A. Slotman, Gert Jan Kremers, J.P. Hoogenboom, A.B. Houtsmuller
Research Group
ImPhys/Microscopy Instrumentation & Techniques
Issue number
11
Volume number
11
DOI:
https://doi.org/10.1242/bio.059417
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Abstract

Focal adhesions (FAs) are the main cellular structures to link the intracellular cytoskeleton to the extracellular matrix. FAs mediate cell adhesion, are important for cell migration and are involved in many (patho)-physiological processes. Here we examined FAs and their associated actin fibres using correlative fluorescence and scanning electron microscopy (SEM). We used fluorescence images of cells expressing paxillin-GFP to define the boundaries of FA complexes in SEM images, without using SEM contrast enhancing stains. We observed that SEM contrast was increased around the actin fibre entry site in 98% of FAs, indicating increases in protein density and possibly also phosphorylation levels in this area. In nearly three quarters of the FAs, these nanostructures had a fork shape, with the actin forming the stem and the high-contrast FA areas the fork. In conclusion, the combination of fluorescent and electron microscopy allowed accurate localisation of a highly abundant, novel fork structure at the FA-actin interface.

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