Electromagnetic wireless remote control of mammalian transgene expression
← Research streamMultiferroic nanoparticles (chitosan-coated) generated cytoplasmic ROS in response to a low-frequency (1-kHz) magnetic field, which was detected by ROS-responsive KEAP1/NRF2 biosensors linked to synthetic promoters to drive transgene expression. In a proof-of…
Study snapshot
Abstract
Category: Nanotechnology, Biomedical Engineering Tags: electromagnetic fields, transgene expression, wireless control, nanotechnology, ROS, gene therapy, biosensors DOI: 10.1038/s41565-025-01929-w URL: nature.com Overview Communication between wireless field receivers and biological sensors remains a key constraint in the development of wireless electronic devices for minimally invasive medical monitoring and biomedical applications involving gene and cell therapies. Innovation This study describes a nanoparticle-cell interface that enables electromagnetic programming of wireless expression regulation (EMPOWER) of transgenes. This is achieved via the biosafe generation of cellular reactive oxygen species (ROS). - Multiferroic nanoparticles are coated with chitosan to improve biocompatibility. - These nanoparticles generate ROS in the cytoplasm of cells in response to a low-frequency (1-kHz) magnetic field. - Overexpressed ROS-responsive KEAP1/NRF2 biosensors detect the generated ROS and are connected to synthetic ROS-responsive promoters to drive transgene expression. Findings In a proof-of-concept study, subcutaneously implanted alginate-microencapsulated cells stably expressing an EMPOWER-controlled insulin expression system successfully normalized blood-glucose levels in a mouse model of type 1 diabetes in response to a weak magnetic field. Conclusion The research demonstrates a wireless and minimally invasive approach to regulate gene expression in vivo using electromagnetic fields, mediated by biocompatible nanoparticles and ROS-sensitive biosensors. This highlights a direct link between electromagnetic field exposure and physiological regulation at the molecular and cellular level, underscoring the potential health and therapeutic implications of EMF exposure.
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
Multiferroic nanoparticles (chitosan-coated) generated cytoplasmic ROS in response to a low-frequency (1-kHz) magnetic field, which was detected by ROS-responsive KEAP1/NRF2 biosensors linked to synthetic promoters to drive transgene expression. In a proof-of-concept mouse model of type 1 diabetes, implanted cells with an EMPOWER-controlled insulin system normalized blood-glucose levels in response to a weak magnetic field.
Outcomes measured
- Transgene expression regulation (insulin expression)
- Blood-glucose levels normalization
- Cellular reactive oxygen species (ROS) generation
Limitations
- Sample size not reported in provided abstract/metadata
- Exposure intensity and duration not specified in provided abstract/metadata
- Proof-of-concept design; generalizability beyond the described model not stated
View raw extracted JSON
{
"study_type": "animal",
"exposure": {
"band": "ELF",
"source": "other",
"frequency_mhz": null,
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},
"population": "Mouse model of type 1 diabetes (subcutaneously implanted alginate-microencapsulated cells)",
"sample_size": null,
"outcomes": [
"Transgene expression regulation (insulin expression)",
"Blood-glucose levels normalization",
"Cellular reactive oxygen species (ROS) generation"
],
"main_findings": "Multiferroic nanoparticles (chitosan-coated) generated cytoplasmic ROS in response to a low-frequency (1-kHz) magnetic field, which was detected by ROS-responsive KEAP1/NRF2 biosensors linked to synthetic promoters to drive transgene expression. In a proof-of-concept mouse model of type 1 diabetes, implanted cells with an EMPOWER-controlled insulin system normalized blood-glucose levels in response to a weak magnetic field.",
"effect_direction": "benefit",
"limitations": [
"Sample size not reported in provided abstract/metadata",
"Exposure intensity and duration not specified in provided abstract/metadata",
"Proof-of-concept design; generalizability beyond the described model not stated"
],
"evidence_strength": "low",
"confidence": 0.74,
"peer_reviewed_likely": "yes",
"keywords": [
"electromagnetic fields",
"magnetic field",
"1-kHz",
"ELF",
"wireless control",
"transgene expression",
"nanoparticles",
"multiferroic nanoparticles",
"chitosan",
"reactive oxygen species",
"ROS",
"KEAP1",
"NRF2",
"biosensor",
"synthetic promoter",
"insulin",
"type 1 diabetes",
"mouse"
],
"suggested_hubs": [
{
"slug": "other",
"weight": 0.4,
"reason": "Biomedical/therapeutic use of low-frequency magnetic fields to control gene expression via nanoparticles; no specific portal hub provided in prompt matches this topic."
}
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}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: 10.1038/s41565-025-01929-w
PubMed: Not supplied
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