Specific low-frequency electromagnetic fields induce expression of active KDM6B associated with functional changes in U937 cells

Abstract

In this study, we investigated the effects of specific low frequency electromagnetic fields sequences on U937 cells, an in vitro model of human monocyte/macrophage differentiation. U937 cells were exposed to electromagnetic stimulation by means of the SynthéXer ® system using two similar sequences, XR-BC31 and XR-BC31/F. Each sequence was a time series of twenty-nine wave segments. Here, we report that exposure (4 days, once a day) of U937 cells to the XR-BC31 setting, but not to the XR-BC31/F, resulted in increased expression of the histone demethylase KDM6B along with a global reduction in histone H3 lysine 27 (H3K27) tri-methylation. Furthermore, exposure to the XR-BC31 sequence induced differentiation of U937 cells towards a macrophage-like phenotype displaying a KDM6B dependent increase in expression and secretion of the anti-inflammatory interleukins (ILs), IL-10 and IL-4. Importantly, all the observed changes were highly dependent on the sequence's nature. Our results open a new way of interpretation for the effects of low frequency electromagnetic fields observed in vivo. Indeed, it is conceivable that a specific low frequency electromagnetic fields treatment may cause changes in chromatin accessibility and consequently in the expression of anti-inflammatory mediators and in cell differentiation.

Magnetic Stimulation Drives Macrophage Polarization in Cell to–Cell Communication with IL-1β Primed Tendon Cells

“…Together with complex dynamics of regulatory signals, modulation of tendon immune biology events, including the switch of macrophage functional phenotypes, may be assisted by external triggers [ 12 ]. Research has shown that the pulsed electromagnetic field (PEMF), a biophysical form of stimulation, accelerates cell differentiation, increases deposition of collagen, and modulates the activation of cell surface receptors, thereby holding relevant contributions for the re-establishment of homeostatic cell functions [ 13 ].…”