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1.
Radiat Res ; 172(6): 725-36, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19929419

RESUMO

Intracellular calcium oscillations have long been recognized as a principal mediator of many vital cellular activities. Furthermore, Ca(2+) dynamics can be modulated by external physical cues, including electromagnetic fields. While cellular responses to low-frequency electric fields have been established, the possible non-thermal effects of millimeter-wave (MMW) radiation are still a subject of discussion and debate. We used mouse embryonic stem cell-derived neuronal cells and a custom-built 94 GHz applicator to examine in real time the altered Ca(2+) oscillations associated with MMW stimulation. MMW irradiation at 18.6 kW/m(2) nominal power density significantly increased the Ca(2+) spiking frequency in the cells exhibiting Ca(2+) activity. The N-type calcium channels, phospholipase C enzyme, and actin cytoskeleton appear to be involved in mediating increased Ca(2+) spiking. Reorganization of the actin microfilaments by a 94 GHz field seems to play a crucial role in modulating not only Ca(2+) activity but also cell biomechanics. Many but not all observed cellular responses to MMW were similar to thermally induced effects. For example, cell exposure to a 94 GHz field induced nitric oxide production in some morphologically distinct neuronal cells that could not be reproduced by thermal heating of the cells up to 42 degrees C. The highest observed average temperature rise in the MMW exposure chamber was approximately 8 degrees C above the room temperature, with possible complex non-uniform microscopic distribution of heating rates at the cell level. Our findings may be useful to establish quantitative molecular benchmarks for elucidation of nociception mechanisms and evaluation of potential adverse bioeffects associated with MMW exposure. Moreover, control of Ca(2+) dynamics by MMW stimulation may offer new tools for regulation of Ca(2+)-dependent cellular and molecular activities, for example, in tissue engineering applications.


Assuntos
Cálcio/metabolismo , Neurônios/efeitos da radiação , Animais , Linhagem Celular Tumoral , Camundongos , Microscopia de Força Atômica , Microscopia Confocal , Neurônios/metabolismo , Óxido Nítrico/biossíntese
2.
Radiat Res ; 169(3): 319-29, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18302487

RESUMO

Intracellular Ca(2+) spikes trigger cell proliferation, differentiation and cytoskeletal reorganization. In addition to Ca(2+) spiking that can be initiated by a ligand binding to its receptor, exposure to electromagnetic stimuli has also been shown to alter Ca(2+) dynamics. Using neuronal cells differentiated from a mouse embryonic stem cell line and a custom-built, frequency-tunable applicator, we examined in real time the altered Ca(2+) dynamics and observed increases in the cytosolic Ca(2+) in response to nonthermal radiofrequency (RF)-radiation exposure of cells from 700 to 1100 MHz. While about 60% of control cells (not exposed to RF radiation) were observed to exhibit about five spontaneous Ca(2+) spikes per cell in 60 min, exposure of cells to an 800 MHz, 0.5 W/kg RF radiation, for example, significantly increased the number of Ca(2+) spikes to 15.7+/-0.8 (P<0.05). The increase in the Ca(2+) spiking activities was dependent on the frequency but not on the SAR between 0.5 to 5 W/kg. Using pharmacological agents, it was found that both the N-type Ca(2+) channels and phospholipase C enzymes appear to be involved in mediating increased Ca(2+) spiking. Interestingly, microfilament disruption also prevented the Ca(2+) spikes. Regulation of Ca(2+) dynamics by external physical stimulation such as RF radiation may provide a noninvasive and useful tool for modulating the Ca(2+)-dependent cellular and molecular activities of cells seeded in a 3D environment for which only a few techniques are currently available to influence the cells.


Assuntos
Sinalização do Cálcio/fisiologia , Sinalização do Cálcio/efeitos da radiação , Cálcio/metabolismo , Neurônios/citologia , Neurônios/fisiologia , Células-Tronco/citologia , Células-Tronco/fisiologia , Animais , Canais de Cálcio Tipo L/fisiologia , Canais de Cálcio Tipo L/efeitos da radiação , Diferenciação Celular/efeitos da radiação , Proliferação de Células/efeitos da radiação , Células Cultivadas , Relação Dose-Resposta à Radiação , Temperatura Alta , Taxa de Depuração Metabólica/efeitos da radiação , Camundongos , Neurônios/efeitos da radiação , Doses de Radiação , Ondas de Rádio , Células-Tronco/efeitos da radiação
3.
ASAIO J ; 47(1): 11-7, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11199307

RESUMO

The influence of surface energy and structural properties of carbon coated polyethylene (PE) on the human platelet adhesion was studied. Three types of amorphous carbon coating were obtained by plasma pulse discharge, with the number of pulses grading as 10, 50, 100. Human serum albumin adsorption experiments have been carried out with all samples in vitro. Platelet adhesion analysis by SEM included determination of total quantity of adherent platelets, and respective quantities of platelets at different stages of activation (single, spread, aggregates). Surface topographies ranged from bare PE and such (10 pulses), to globular 0.5 microm in size (50 pulses), and complex fibrillar 3-4 microm structures (100 pulses). Surface free energy varies from 31.7 +/- 0.6 to 40.4 +/- 0.6 mN/m for uncoated PE and 10 pulse coatings, respectively, as determined by contact angle techniques. All studied coatings demonstrate weaker platelet activation properties in comparison with untreated PE. Among all studied coatings, the 50 pulse coated surface seems to be the least suitable for contact with platelets, mainly due to its structural rather than to its energy properties. These data are related to a sharp decrease in the adsorbed protein level for the samples with 50 pulse coatings. The applied analysis of platelet activation enables more accurate characterization of platelet-biomaterial interaction.


Assuntos
Carbono/farmacologia , Adesividade Plaquetária/efeitos dos fármacos , Polietileno/farmacologia , Propriedades de Superfície/efeitos dos fármacos , Adsorção/efeitos dos fármacos , Humanos , Técnicas In Vitro , Cinética , Teste de Materiais , Albumina Sérica/farmacocinética
4.
Med Tekh ; (1): 6-9, 1998.
Artigo em Russo | MEDLINE | ID: mdl-9560811

RESUMO

The paper deals with the methodological features of investigations of the interaction of cells and foreign material surfaces by scanning electron microscopy. The proposed technique for obtaining electron microscopic images results in their easy binarization and further treatment using computer software. The specificity of obtaining electron microphotographs permits detailed quantitative image analysis. This approach enables one to study both quantity of objects and their individual morphologies, as well as to define distributions of objects by their diameter, area, etc. Human platelet adhesion to glass and metal is considered as an example.


Assuntos
Adesão Celular , Processamento de Imagem Assistida por Computador , Microscopia Eletrônica de Varredura , Adesividade Plaquetária , Alumínio , Vidro , Humanos , Fotomicrografia , Software , Fatores de Tempo
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