Inability of 50 Hz magnetic fields to regulate PKC- and Ca(2+)-dependent gene expression in Jurkat cells.
← Research streamIn transiently transfected Jurkat cells carrying calcium-ion dependent luciferase reporter constructs, exposure to a sinusoidal 50 Hz magnetic field showed no indication of influencing reporter activity, either alone or combined with ionomycin, phorbol ester,…
Study snapshot
Abstract
We have previously reported that the T cell line Jurkat registers the exposure of a sinusoidal extremely low frequency magnetic field at the level of the plasma membrane, resulting in activation of the tyrosine kinase p56(lck), increase in inositol-3-phosphate levels and increase in intracellular calcium concentration within minutes. To elucidate if these events associated with changes in intracellular calcium ion levels were biologically significant, transient transfections of Jurkat cells were performed with calcium-ion dependent reporter constructs. Three different enhancer/promoter constructs were studied coupled to the luciferase reporter gene. The luciferase activity of each construct was measured after treatment of transfected cells to EMF exposure alone, or in combination with ionomycin, phorbol ester or cross-linking anti-CD3 antibodies. There was no indication that the used EMFs could influence any of these reporter constructs.
AI evidence extraction
Structured fields below were generated from the paper’s abstract and metadata to make the evidence easier to inspect. Automated extraction may be incomplete or incorrect; verify important details against the original paper.
Main findings
In transiently transfected Jurkat cells carrying calcium-ion dependent luciferase reporter constructs, exposure to a sinusoidal 50 Hz magnetic field showed no indication of influencing reporter activity, either alone or combined with ionomycin, phorbol ester, or anti-CD3 cross-linking.
Outcomes measured
- Luciferase reporter activity from Ca(2+)-dependent enhancer/promoter constructs (gene expression reporters)
Limitations
- Exposure parameters beyond frequency (e.g., field strength, duration) not reported in the abstract
- Sample size and replication details not reported in the abstract
- Only reporter constructs in Jurkat cells were assessed; generalizability to other cell types/endpoints is not addressed in the abstract
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": 0.05,
"sar_wkg": null,
"duration": null
},
"population": "Jurkat T cell line (Jurkat cells)",
"sample_size": null,
"outcomes": [
"Luciferase reporter activity from Ca(2+)-dependent enhancer/promoter constructs (gene expression reporters)"
],
"main_findings": "In transiently transfected Jurkat cells carrying calcium-ion dependent luciferase reporter constructs, exposure to a sinusoidal 50 Hz magnetic field showed no indication of influencing reporter activity, either alone or combined with ionomycin, phorbol ester, or anti-CD3 cross-linking.",
"effect_direction": "no_effect",
"limitations": [
"Exposure parameters beyond frequency (e.g., field strength, duration) not reported in the abstract",
"Sample size and replication details not reported in the abstract",
"Only reporter constructs in Jurkat cells were assessed; generalizability to other cell types/endpoints is not addressed in the abstract"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"extremely low frequency",
"ELF",
"50 Hz",
"magnetic field",
"Jurkat cells",
"T cell line",
"calcium-dependent gene expression",
"PKC",
"Ca2+",
"luciferase reporter",
"transient transfection",
"ionomycin",
"phorbol ester",
"anti-CD3",
"p56(lck)"
],
"suggested_hubs": [
{
"slug": "occupational-exposure",
"weight": 0.2,
"reason": "Study involves 50 Hz ELF magnetic fields, which are commonly discussed in occupational ELF exposure contexts, though no specific occupational setting is described."
}
]
}AI-extracted fields are generated from the abstract and metadata and may be incomplete or incorrect. This material is for informational purposes and is not medical advice.
Identifiers and source
DOI: 10.1006/cbir.2001.0837
PubMed: 11846450
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