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Fractal analysis of cell boundary ultrastructure imaged by atomic force microscopy

Authors
Kim, Yu JinKim, Hee-DaeKim, Hyun HeeShin, Sang-MoKang, Chi JungLee, Kun Ho
Issue Date
4-May-2015
Publisher
TAYLOR & FRANCIS LTD
Keywords
fractal analysis; atomic force microscopy; filopodia; lamellipodia; actin cytoskeleton
Citation
ANIMAL CELLS AND SYSTEMS, v.19, no.3, pp.161 - 167
Indexed
SCIE
SCOPUS
KCI
Journal Title
ANIMAL CELLS AND SYSTEMS
Volume
19
Number
3
Start Page
161
End Page
167
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/93590
DOI
10.1080/19768354.2015.1037347
ISSN
1976-8354
Abstract
Fractal analysis has been widely used to determine the complexity of irregular shapes of various natural objects including biological systems. Here we report an investigation into the nature of the cell boundary nanostructure (less than 200 nm in thickness) in an aqueous environment using atomic force microscopy. The box-counting method revealed the fractal nature of detailed contours of cells cultured on a solid substratum. The fractal dimensions (D-f) of individual cells of the human epithelial cell line MCF10A converged on a narrow range (D-f = 1.352 +/- 0.044) despite their morphological diversity. Treatment with cytochalasin D, an inhibitor of actin polymerization, was shown to decrease both the ruggedness and the D-f of cell boundaries. These findings suggest that the D-f value is a useful parameter for describing the complexity of cellular ultrastructure dependent on the actin cytoskeleton.
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