Continuous exposure to 900MHz GSM-modulated EMF alters morphological maturation of neural cells

Neurosci Lett. 2009 May 22;455(3):173-7. doi: 10.1016/j.neulet.2009.03.061. Epub 2009 Mar 24.

Abstract

The effects of radiofrequency electromagnetic field (RF-EMF) exposure on neuronal phenotype maturation have been studied in two different in vitro models: murine SN56 cholinergic cell line and rat primary cortical neurons. The samples were exposed at a dose of 1W/kg at 900 MHz GSM modulated. The phenotype analysis was carried out at 48 and 72 h (24 and 48 h of SN56 cell line differentiation) or at 24, 72, 120 h (2, 4 and 6 days in vitro for cortical neurons) of exposure, on live and immunolabeled neurons, and included the morphological study of neurite emission, outgrowth and branching. Moreover, cortical neurons were studied to detect alterations in the expression pattern of cytoskeleton regulating factors, e.g. beta-thymosin, and of early genes, e.g. c-Fos and c-Jun through real-time PCR on mRNA extracted after 24h exposure to EMF. We found that RF-EMF exposure reduced the number of neurites generated by both cell systems, and this alteration correlates to increased expression of beta-thymosin mRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / radiation effects
  • Cell Line
  • Central Nervous System / growth & development*
  • Central Nervous System / pathology
  • Central Nervous System / radiation effects*
  • Electromagnetic Fields / adverse effects*
  • Mice
  • Neurites / metabolism
  • Neurites / pathology
  • Neurites / radiation effects
  • Neurogenesis / physiology
  • Neurogenesis / radiation effects*
  • Neurons / metabolism
  • Neurons / pathology
  • Neurons / radiation effects*
  • Proto-Oncogene Proteins c-fos / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cells / metabolism
  • Stem Cells / pathology
  • Stem Cells / radiation effects*
  • Thymosin / analogs & derivatives
  • Thymosin / metabolism
  • Ubiquitins / metabolism

Substances

  • Proto-Oncogene Proteins c-fos
  • RNA, Messenger
  • Ubiquitins
  • thymosin beta(1)
  • Thymosin