Related Experiment Video
Updated: Jul 4, 2026

Functionalization of Atomic Force Microscope Cantilevers with Single-T Cells or Single-Particle for Immunological Single-Cell Force Spectroscopy
Published on: July 10, 2019
Intercellular interaction observed by atomic force microscopy
Su-Jin Kim1, Sejin Kim, Hyunjung Shin
1Department of Anatomy, Korea University College of Medicine, Seoul 136-705, Republic of Korea.
Abstract:
The cultured myoblasts, focusing on the microprocesses related to the intercellular interaction, were observed by taking topological images. For atomic force microscopy (AFM), cells were fixed and either dried as in usual scanning electron microscopy or kept in the buffer. The dried cells were used for observing intercellular interactions related to the fusion. The prefusing myoblasts aligned in a chain were mostly spindle in shape and were characterized by the presence of many microprocesses along the facing edges of adjacent aligned myoblasts. The space between fusing myoblasts and between myotubes and myoblasts were often traversed by filopodia and cellular bridges formed by the connection of microvilli. These results suggest that microprocesses may be involved in the fusion of myoblasts. The best images of the fixed cell in liquid were obtained using the contact mode of AFM. AFM observation is an efficient tool in the study on the interaction between cells, and the fixation, imaging in liquid is a good approach to understand the cellular dynamics.
Insights
Microprocesses on cultured myoblasts, observed using atomic force microscopy (AFM), appear crucial for cell fusion. These cellular extensions facilitate intercellular interactions during myoblast fusion, revealing dynamics of cell-cell communication.
Area of Science:
- Cell Biology
- Biophysics
Background:
- Understanding intercellular interactions is key to cell fusion processes.
- Myoblast fusion is essential for muscle development and regeneration.
Purpose of the Study:
- To investigate the role of microprocesses in myoblast fusion.
- To evaluate atomic force microscopy (AFM) for observing cell dynamics.
Main Methods:
- Cultured myoblasts were observed using topological imaging.
- Atomic force microscopy (AFM) was employed on fixed cells, both dried and in buffer.
- Contact mode AFM was used for imaging fixed cells in liquid.
Main Results:
- Prefusing myoblasts formed chains with numerous microprocesses along adjacent edges.
- Filopodia and microvilli-connected cellular bridges spanned spaces between fusing cells.
- AFM in liquid provided optimal imaging of cellular dynamics.
Conclusions:
- Microprocesses likely play a significant role in myoblast fusion.
- AFM is an effective tool for studying cell-cell interactions.
- Imaging fixed cells in liquid is a valuable method for understanding cellular dynamics.
Related Concept Videos
Atomic Force Microscopy
The AFM Probe
The probe is regarded as the heart of any AFM setup and comprises the...
Studying the Cytoskeleton
Overview of Cell-Matrix Interactions

