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Intercellular interaction observed by atomic force microscopy

Authors
Kim, Su-JinKim, SejinShin, HyunjungUhm, Chang-Sub
Issue Date
9월-2008
Publisher
ELSEVIER SCIENCE BV
Keywords
scanning probe microscopy; biological materials; sensors; nanostructures; biochips; culture; cellular interaction
Citation
ULTRAMICROSCOPY, v.108, no.10, pp.1148 - 1151
Indexed
SCIE
SCOPUS
Journal Title
ULTRAMICROSCOPY
Volume
108
Number
10
Start Page
1148
End Page
1151
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/122776
DOI
10.1016/j.ultramic.2008.04.081
ISSN
0304-3991
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 good approach to understand the cellular dynamics. (C) 2008 Elsevier B.V. All rights reserved.
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의과대학 (의학과)
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