I Hrazdira1, J Skorpíková, M Dolníková. 1. Department of Biophysics, Faculty of Medicine, Masaryk University, Jostova 10, CZ 662 43 Brno, Czech Republic.
Abstract
OBJECTIVE: The aim of this study was to establish: (i) which phase of the cell cycle is most sensitive to ultrasonic action; and (ii) whether and in which way ultrasound can influence components of the cytoskeleton. METHODS: HeLa cell monolayers grown on glass cover-slips in DEM medium were used in all experiments. For proliferation studies, the cell monolayers were trypsinized and the cells were resuspended in fresh medium. The structure of the cytoskeleton was studied by means of the indirect immunofluorescence method. The cells were sonicated by a cw ultrasound of 0.8 MHz at low SA intensities (50, 100 and 500 mW/cm2) for 5 and 10 min. RESULTS: The analysis of proliferation demonstrated that cells were most sensitive when undergoing M- and S-phases of the cell cycle. The ultrasonically induced disassembly of cytoskeleton components was most marked in microtubules and microfilaments due to depolymerization of basic proteins (tubulin and actin). The reaction of intermediate filaments was distinctly weaker. CONCLUSIONS: In-vitro treatment of tumour cells with low intensity ultrasound results in partial inhibition of proliferation as well as in partial disassembly of all components of the cytoskeleton. Ultrasonically induced changes of the cytoskeleton seem to be non-specific and temporary. Copyright 1998 Elsevier Science Ireland Ltd.
OBJECTIVE: The aim of this study was to establish: (i) which phase of the cell cycle is most sensitive to ultrasonic action; and (ii) whether and in which way ultrasound can influence components of the cytoskeleton. METHODS: HeLa cell monolayers grown on glass cover-slips in DEM medium were used in all experiments. For proliferation studies, the cell monolayers were trypsinized and the cells were resuspended in fresh medium. The structure of the cytoskeleton was studied by means of the indirect immunofluorescence method. The cells were sonicated by a cw ultrasound of 0.8 MHz at low SA intensities (50, 100 and 500 mW/cm2) for 5 and 10 min. RESULTS: The analysis of proliferation demonstrated that cells were most sensitive when undergoing M- and S-phases of the cell cycle. The ultrasonically induced disassembly of cytoskeleton components was most marked in microtubules and microfilaments due to depolymerization of basic proteins (tubulin and actin). The reaction of intermediate filaments was distinctly weaker. CONCLUSIONS: In-vitro treatment of tumour cells with low intensity ultrasound results in partial inhibition of proliferation as well as in partial disassembly of all components of the cytoskeleton. Ultrasonically induced changes of the cytoskeleton seem to be non-specific and temporary. Copyright 1998 Elsevier Science Ireland Ltd.
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