Effects of exposure to a time-varying 1.5 T magnetic field on the neurotransmitter-activated increase in intracellular Ca(2+) in relation to actin fiber and mitochondrial functions in bovine adrenal chromaffin cells

Biochim Biophys Acta. 2010 Dec;1800(12):1221-30. doi: 10.1016/j.bbagen.2010.09.001. Epub 2010 Sep 9.

Abstract

Background: It has been reported that exposure to electromagnetic fields influences intracellular signal transduction. We studied the effects of exposure to a time-varying 1.5 T magnetic field on membrane properties, membrane cation transport and intracellular Ca(2+) mobilization in relation to signals. We also studied the mechanism of the effect of exposure to the magnetic field on intracellular Ca(2+) release from Ca(2+) stores in adrenal chromaffin cells.

Methods: We measured the physiological functions of ER, actin protein, and mitochondria with respect to a neurotransmitter-induced increase in Ca(2+) in chromaffin cells exposed to the time-varying 1.5 T magnetic field for 2h.

Results: Exposure to the magnetic field significantly reduced the increase in [Ca(2+)]i. The exposure depolarized the mitochondria membrane and lowered oxygen uptake, but did not reduce the intracellular ATP content. Magnetic field-exposure caused a morphological change in intracellular F-actin. F-actin in exposed cells seemed to be less dense than in control cells, but the decrease was smaller than that in cytochalasin D-treated cells. The increase in G-actin (i.e., the decrease in F-actin) due to exposure was recovered by jasplakinolide, but inhibition of Ca(2+) release by the exposure was unaffected.

Conclusions and general significance: These results suggest that the magnetic field-exposure influenced both the ER and mitochondria, but the inhibition of Ca(2+) release from ER was not due to mitochondria inhibition. The effect of eddy currents induced in the culture medium may indirectly influence intracellular actin and suppress the transient increase in [Ca(2+)]i.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology*
  • Actin Cytoskeleton / drug effects*
  • Actin Cytoskeleton / metabolism
  • Actins / metabolism
  • Adenosine Triphosphate / metabolism
  • Adrenal Glands / cytology
  • Animals
  • Calcium / metabolism*
  • Cattle
  • Cells, Cultured
  • Chromaffin Cells / cytology
  • Chromaffin Cells / drug effects*
  • Chromaffin Cells / metabolism
  • Colchicine / pharmacology
  • Cytochalasin D / pharmacology
  • Depsipeptides / pharmacology
  • Electromagnetic Fields*
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / metabolism
  • Immunoblotting
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism
  • Membrane Potential, Mitochondrial / drug effects
  • Microscopy, Confocal
  • Mitochondria / drug effects
  • Mitochondria / physiology
  • Neurotransmitter Agents / pharmacology
  • Nucleic Acid Synthesis Inhibitors / pharmacology
  • Oxygen Consumption / drug effects
  • Time Factors
  • Tubulin Modulators / pharmacology

Substances

  • Actins
  • Depsipeptides
  • Neurotransmitter Agents
  • Nucleic Acid Synthesis Inhibitors
  • Tubulin Modulators
  • jasplakinolide
  • Cytochalasin D
  • Adenosine Triphosphate
  • Acetylcholine
  • Colchicine
  • Calcium