Proteomic Analysis of the Response of Human Endothelial
Cell Line EA.hy926 to 1800 GSM Mobile Phone Radiation |
| Reetta Nylund1, Hanna Tammio1, Niels Kuster2, Dariusz Leszczynski1,* |
1STUK - Radiation and Nuclear Safety Authority, Helsinki, Finland |
2IT’IS Foundation, Swiss Federal Institute of Technology, Zurich, Switzerland |
| *Corresponding author: |
Dr. Dariusz Leszczynski, PhD,
STUK-Radiation
and Nuclear Safety Authority,
Laippatie 4, 00880 Helsinki, Finland,
E-mail: dariusz.leszczynski@stuk.fi |
|
| Received September 22, 2009; Accepted October 26, 2009; Published
October 26, 2009 |
Citation: Nylund R, Tammio H, Kuster N, Leszczynski D (2009) Proteomic
Analysis of the Response of Human Endothelial Cell Line EA.hy926 to
1800 GSM Mobile Phone Radiation. J Proteomics Bioinform 2: 455-462. doi:10.4172/jpb.1000105 |
Copyright: ©2009 Nylund R, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author
and source are credited. |
| Abstract |
Background: We have earlier shown that exposure of
human endothelial cell line EA.hy926 to 900 MHz GSM
mobile phone radiation causes changes in the expression
of numerous proteins. Here, we have examined the effects
of 1800 MHz GSM mobile phone signal on the proteome
of the same cell line.
Results: EA.hy926 cells were exposed for one hour to
1800 MHz GSM signal, simulating mobile phone talking
conditions, at an average specific absorption rate (SAR)
of 2.0 W/kg at 37±0.3°C. Sham samples were produced
simultaneously in the same conditions but without the
radiation exposure. Cells were harvested immediately after
1-hour exposure to the radiation, and proteins were
extracted and separated using 2-dimensional
electrophoresis (2DE). In total, 10 experimental replicates
were generated from both exposed and sham samples.
About 900 protein spots were detected in the 2DE-gels
using PDQuest software and eight of them were found to
be differentially expressed in exposed cells (p<0.05, t-test).
Three out of these eight proteins were identified using
Maldi-ToF mass spectrometry (MS). These proteins are:
spermidine synthase (SRM), 78 kDa glucose-regulated
protein (55 kDa fragment) (GRP78) and proteasome
subunit alpha type 1 (PSA1). Due to the lack of the
availability of commercial antibodies we were able to
further examine expression of only GRP78. Using SDSPAGE
and western blot method we were not able to confirm
the result obtained for GRP78 using 2DE. Additionally,
we have not seen any effect of 1800GSM exposure on the
expression of vimentin and Hsp27 - proteins that were
affected by the 900 MHz GSM exposure in our earlier
studies.
Conclusions: Our results suggest that the 900GSM and
1800GSM exposures might affect the expression of some
proteins in the EA.hy926 cell line. The observed here
discrepancy between the expression changes of GRP78
detected with 1DE and 2DE confirms the importance of
validation of the results obtained with 2DE using other
methods, e.g. western blot. |
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