DocumentCode :
1447575
Title :
Fractal Dimension as a Measure of Altered Actin Cytoskeleton in MC3T3-E1 Cells Under Simulated Microgravity Using 3-D/2-D Clinostats
Author :
Qian, A.R. ; Li, D. ; Han, J. ; Gao, X. ; Di, S.M. ; Zhang, W. ; Hu, L.F. ; Shang, Peng
Author_Institution :
Key Lab. for Space Biosci. & Biotechnol., Northwestern Polytech. Univ., Xi´´an, China
Volume :
59
Issue :
5
fYear :
2012
fDate :
5/1/2012 12:00:00 AM
Firstpage :
1374
Lastpage :
1380
Abstract :
Osteoblasts, the bone-forming cells, respond to various mechanical forces, such as stretch and fluid shear force in essentially similar ways. The cytoskeleton, as the load-bearing architecture of the cell, is sensitive to altered inertial forces. Disruption of the cytoskeleton will result in alteration of cellular structure and function. However, it is difficult to quantitatively illustrate cytoskeletal rearrangement because of the complexity of cytoskeletal structure. Usually, the morphological changes in actin organization caused by external stimulus are basically descriptive. In this study, fractal dimensions (D) analysis was used to quantify the morphological changes in the actin cytoskeleton of osteoblast-like cells (MC3T3-E1) under simulated microgravity using 3-D/2-D clinostats. The ImageJ software was used to count the fractal dimension of actin cytoskeleton by box-counting methods. Real-time PCR and immunofluroscent assays were used to further confirm the results obtained by fractal dimension analysis. The results showed significant decreases in D value of actin cytoskeleton, β-actin mRNA expression, and the mean fluorescence intensity of F-actin in osteoblast-like cells after 24 or 48 h of incubation under 3-D/2-D clinorotation condition compared with control. The findings indicate that 3-D/2-D clinorotation affects both actin cytoskeleton architecture and mRNA expression, and fractal may be a promising approach for quantitative analysis of the changes in cytoskeleton in different environments.
Keywords :
RNA; biomechanics; bone; cellular biophysics; fluorescence; fractals; molecular biophysics; shear flow; zero gravity experiments; β-actin mRNA expression; 3-D-2-D clinostats; ImageJ software; MC3T3-E1 cells; altered actin cytoskeleton; bone-forming cells; box-counting methods; cellular function; cellular structure; fluid shear force; fractal dimension; immunofluroscent assays; mean fluorescence intensity; mechanical forces; osteoblasts; simulated microgravity; time 24 hr; time 48 hr; Cells (biology); Complexity theory; Fluorescence; Fractals; Gravity; Real time systems; Software; Actin cytoskeleton; clinorotation; fractal dimension; osteoblast; simulated microgravity; Actin Cytoskeleton; Actins; Animals; Cell Culture Techniques; Cell Line; Fractals; Mice; Microscopy, Confocal; Microscopy, Fluorescence; Osteoblasts; Real-Time Polymerase Chain Reaction; Weightlessness;
fLanguage :
English
Journal_Title :
Biomedical Engineering, IEEE Transactions on
Publisher :
ieee
ISSN :
0018-9294
Type :
jour
DOI :
10.1109/TBME.2012.2187785
Filename :
6151816
Link To Document :
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