We investigated whether static electromagnetic fields (EMFs) at a flux density of 4.75 T, generated by
an NMR apparatus (NMRF), could promote movements of Ca2þ, cell proliferation, and the eventual
production of proinflammatory cytokines in human peripheral blood mononuclear cells (PBMC) as
well as in Jurkat cells, after exposure to the field for 1 h. The same study was also performed after
activation of cells with 5 mg/ml phytohaemagglutinin (PHA). Our results clearly demonstrate that
static NMRF exposure has neither proliferative, nor activating, nor proinflammatory effects on both
normal and PHA activated PBMC. Moreover, the concentration of interleukin-1b, interleukin-2,
interleukin-6, interferon, and tumour necrosis factor a (TNFa) remained unvaried in exposed cells.
Exposure of Jurkat cells statistically decreased the proliferation and the proliferation indexes, which
24 and 48 h after exposure were 0.70.29 and 0.870.12, respectively. Moreover, in Jurkat cells
the [Ca2þ]i was higher than in PBMC and was reduced significantly to about one half after exposure.
This is consistent with the decrease of proliferation and with the low levels of IL-2 measured. On the
whole, our data suggest that NMRF exposure failed to affect the physiologic behaviour of normal
lymphomonocytes. Instead in Jurkat cells, by changing the properties of cell membranes, NMRF can
influence Ca2þ transport processes, and hence Ca2þ homeostasis with improvement of proliferation
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