TY - JOUR
T1 - Static magnetic fields affect calcium fluxes and inhibit stress-induced apoptosis in human glioblastoma cells
AU - Teodori, Laura
AU - Göhde, Wolfgang
AU - Valente, Maria Giovanna
AU - Tagliaferri, Fausto
AU - Coletti, Dario
AU - Perniconi, Barbara
AU - Bergamaschi, Antonio
AU - Cerella, Claudia
AU - Ghibelli, Lina
PY - 2002/12/1
Y1 - 2002/12/1
N2 - Background: Epidemiologic data revealed increased brain tumor incidence in workers exposed to magnetic fields (MFs), raising concerns about the possible link between MF exposure and cancer. However, MFs seem to be neither mutagenic nor tumorigenic. The mechanism of their tumorigenic effect has not been elucidated. Methods: To evaluate the interference of MFs with physical (heat shock, HS) and chemical (etoposide, VP16) induced apoptoses, respectively, we exposed a human glioblastoma primary culture to 6 mT static MF. We investigated cytosolic Ca2+ ([Ca2+]i) fluxes and extent of apoptosis as key endpoints. The effect of MFs on HS- and VP16-induced apoptoses in primary glioblastoma cultures from four patients was also tested. Results: Static MFs increased the [Ca2+]i from a basal value of 124 ± 4 nM to 233 ± 43 nM (P < 0.05). MF exposure dramatically reduced the extent of HS- and VP16-induced apoptoses in all four glioblastoma primary cultures analyzed by 56% (range, 28-87%) and 44% (range, 38-48%), respectively. However, MF alone did not exert any apoptogenic activity. Differences were observed across the four cultures with regard to apoptotic induction by HS and VP16 and to MF apoptotic reduction, with an individual variability with regard to apoptotic sensitivity. Conclusion: The ability of static MFs to reduce the extent of damage-induced apoptosis in glioblastoma cells might allow the survival of damaged and possibly mutated cells.
AB - Background: Epidemiologic data revealed increased brain tumor incidence in workers exposed to magnetic fields (MFs), raising concerns about the possible link between MF exposure and cancer. However, MFs seem to be neither mutagenic nor tumorigenic. The mechanism of their tumorigenic effect has not been elucidated. Methods: To evaluate the interference of MFs with physical (heat shock, HS) and chemical (etoposide, VP16) induced apoptoses, respectively, we exposed a human glioblastoma primary culture to 6 mT static MF. We investigated cytosolic Ca2+ ([Ca2+]i) fluxes and extent of apoptosis as key endpoints. The effect of MFs on HS- and VP16-induced apoptoses in primary glioblastoma cultures from four patients was also tested. Results: Static MFs increased the [Ca2+]i from a basal value of 124 ± 4 nM to 233 ± 43 nM (P < 0.05). MF exposure dramatically reduced the extent of HS- and VP16-induced apoptoses in all four glioblastoma primary cultures analyzed by 56% (range, 28-87%) and 44% (range, 38-48%), respectively. However, MF alone did not exert any apoptogenic activity. Differences were observed across the four cultures with regard to apoptotic induction by HS and VP16 and to MF apoptotic reduction, with an individual variability with regard to apoptotic sensitivity. Conclusion: The ability of static MFs to reduce the extent of damage-induced apoptosis in glioblastoma cells might allow the survival of damaged and possibly mutated cells.
KW - Apoptosis
KW - Calcium fluxes
KW - Chemical and physical stresses
KW - Flow cytometry
KW - Human glioblastoma cells
KW - Microfluorometry
KW - Static magnetic fields
UR - http://www.scopus.com/inward/record.url?scp=0042738014&partnerID=8YFLogxK
U2 - 10.1002/cyto.10172
DO - 10.1002/cyto.10172
M3 - Article
C2 - 12454977
AN - SCOPUS:0042738014
SN - 0196-4763
VL - 49
SP - 143
EP - 149
JO - Cytometry
JF - Cytometry
IS - 4
ER -