Study type: Medical/biological study (experimental study)

17-Estradiol Counteracts the Effects of High Frequency Electromagnetic Fields on Trophoblastic Connexins and Integrins med./bio.

Published in: Oxid Med Cell Longev 2013: 280850

Aim of study (acc. to author)

To examine whether radiofrequency electromagnetic fields and estradiol regulate cell-cell and cell-extracellular matrix interactions in a trophoblast cell line as a model for the early development of the placenta during gestation.

Background/further details

A critical step in the development of the human placenta is the differentiation of trophoblast stem cells. In this process the trophoblast cells and the extracellular matrix are included, which interact with diverse adhesion molecules such as connexins and integrins. Integrins are transmembrane proteins that mediate the attachment between cells as well as between cells and the extracellular matrix. Therefore, the effects of radiofrequency fields and estradiol on connexins, integrins and estrogen receptor gene expression and protein expression were studied, as well as on ultrastructural cell features in gestational tissue (trophoblast cell line).
Cell cultures were subjected to different treatment conditions: 1.) sham exposure, 2.) radiofrequency exposure, 3.) addition of 17-estradiol into the culture medium (10-6 M) and 4.) combination of radiofrequency exposure + addition of 17-estradiol (10-6 M).



Exposure Parameters
Exposure 1: 1,800 MHz
Modulation type: pulsed
Exposure duration: continuous for 1 h
  • SAR: 2 W/kg average over time

General information

Cells were exposed in 4 groups: 1.) sham exposure, 2.) radiofrequency exposure, 3.) addition of 17-estradiol into the culture medium, 4.) co-exposure of radiofrequency exposure + addition of 17-estradiol.

Exposure 1

Main characteristics
Frequency 1,800 MHz
Exposure duration continuous for 1 h
Modulation type pulsed
Repetition frequency 217 Hz
Pulse type rectangular
Exposure setup
Exposure source
Setup two 128.5 mm x 65 mm x 424 mm brass single mode waveguide resonators; 6 petri dishes kept on plastic holders inside the resonators at the H-field maximum of the standing wave
Sham exposure A sham exposure was conducted.
Measurand Value Type Method Mass Remarks
SAR 2 W/kg average over time measured - -

Reference articles

  • Valbonesi P et al. (2008): Evaluation of HSP70 expression and DNA damage in cells of a human trophoblast cell line exposed to 1.8 GHz amplitude-modulated radiofrequency fields

Exposed system:

Methods Endpoint/measurement parameters/methodology

Investigated system:
Time of investigation:
  • after exposure

Main outcome of study (acc. to author)

Radiofrequency exposure, an addition of estradiol and their combination significantly increased gene expression of connexin 40 and connexin 43 in comparison to the control group. Radiofrequency exposure alone significantly decreased the gene expression of integrins (alpha1, alpha5, beta1) and estrogen receptor beta compared to the control group, while an addition of estradiol or a combination of estradiol with radiofrequency exposure led to a significant increase. No changes occurred regarding protein expression.
In the sham exposed and the radiofrequency exposed cell cultures, the estrogen receptor beta was mainly localized in the cytoplasm, while in the cell cultures treated with estradiol and with a combination of estradiol and radiofrequency exposure, it was mainly concentrated in the nuclear region.
Electron microscopy showed a decrease in cellular adhesion in the radiofrequency exposed cell culture compared to the sham exposed cultures, while an addition of estradiol prevented this effect.
The data indicate that exposure of trophoblasts to radiofrequency electromagnetic fields could modify gene expression and cellular ultrastructure. However, an addition of 17-estradiol could prevent these effects.

Study character:

Study funded by

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