• 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