Human HL-60 cells were exposed for 20 min to an electromagnetic field at frequencies ranging from 15 to 150 Hz and at densities from 0.2 to 2.3 mT (2 to 23 gauss). Following each exposure, quantitative levels of c-myc and histone H2B transcripts were determined by dot-blot hybridization analyses and
Changes in polyamines, c-myc and c-fos gene expression in osteoblast-like cells exposed to pulsed electromagnetic fields
✍ Scribed by Monica De Mattei; Nicoletta Gagliano; Claudia Moscheni; Claudia Dellavia; Carla Calastrini; Agnese Pellati; Magda Gioia; Angelo Caruso; Giordano Stabellini
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 137 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0197-8462
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✦ Synopsis
Abstract
Pulsed electromagnetic field (PEMF) stimulation promotes the healing of fractures in humans, though its effect is little known. The processes of tissue repair include protein synthesis and cell differentiation. The polyamines (PA) are compounds playing a relevant role in both protein synthesis processes and cell differentiation through c‐myc and c‐fos gene activation. Since several studies have demonstrated that PEMF acts on embryonic bone cells, human osteoblast‐like cells and osteosarcoma TE‐85 cell line, in this study we analyzed the effect on cell PAs, proliferation, and c‐myc and c‐fos gene expression of MG‐63 human osteoblast‐like cell cultures exposed to a clinically useful PEMF. The cells were grown in medium with 0.5 or 10% fetal calf serum (FCS). c‐myc and c‐fos gene expressions were determined by RT‐PCR. Putrescine (PUT), spermidine (SPD), or spermine (SPM) levels were evaluated by HPLC. [^3^H]‐thymidine was added to cultures for DNA analysis. The PEMF increased [^3^H]‐thymidine incorporation (P ≤ .01), while PUT decreased after treatment (P ≤ .01); SPM and SPD were not significantly affected. c‐myc was activated after 1 h and downregulated thereafter, while c‐fos mRNA levels increased after 0.5 h and then decreased. PUT, SPD, SPM trends, and [^3^H]‐thymidine incorporation were significantly related to PEMF treatment. These results indicate that exposure to PEMF exerts biological effects on the intracellular PUT of MG‐63 cells and DNA synthesis, influencing the genes encoding c‐myc and c‐fos gene expression. These observations provide evidence that in vitro PEMF affects the mechanisms involved in cell proliferation and differentiation. Bioelectromagnetics 26:207–214, 2005. © 2005 Wiley‐Liss, Inc.
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