Electromagnetic field (50 Hz) enhance metabolic potential and induce adaptive/reprogramming response mediated by the increase of N6-methyladenosine RNA methylation in adipose-derived mesenchymal stem cells in vitro.
Abstract
BACKGROUND: Electromagnetic fields (EMF) have an impact on numerous cellular processes. It can positively and negatively affect adipose-derived stem cells (ASCs) thus their fate through the influence of specific factors and protein secretion. EMF can be a great factor for preconditioning ASCs for regenerative medicine purposes, however, understanding the cell's biological response to its effects in vitro is essential. METHODS: ASCs were exposed to the EMF (50 Hz; 1.5 mT) for 24 and 48 h, and then cell biological response was analyzed. RESULTS: 24 h exposure of ASCs to EMF, significantly increased N6-methyladenosine (mA) RNA methylation, indicating epitranscriptomic changes as an important factor in ASCs preconditioning. Furthermore, the expression of stem cell markers such as Nanog, Oct-4, Sox-2, CD44, and CD105 increased after 24 h of EMF exposure. Besides, western blot analysis showed upregulation of p21 and DNMT2/TRDMT1 protein levels compared to control cells with no differences in the p53 profile. Moreover, after 24 h of exposure to EMF, cell membrane flexibility, the metabolic potential of cells as well as the distribution, morphology, and metabolism of mitochondria were altered. CONCLUSION: ASCs undergo a process of mobilization and adaptation under the EMF influence through the increased mA RNA modifications. These conditions may "force" ASCs to redefine their stem cell fate mediated by RNA-modifying enzymes and alter their reprogramming decision of as differentiation begins.
AI evidence extraction
Main findings
ASCs exposed to 50 Hz, 1.5 mT EMF showed a significant increase in N6-methyladenosine RNA methylation after 24 h. After 24 h exposure, stem cell marker expression increased, p21 and DNMT2/TRDMT1 protein levels were upregulated with no differences in p53 profile, and cell membrane flexibility, metabolic potential, and mitochondrial characteristics were altered.
Outcomes measured
- N6-methyladenosine (mA) RNA methylation
- Stem cell marker expression (Nanog, Oct-4, Sox-2, CD44, CD105)
- Protein levels (p21, DNMT2/TRDMT1, p53)
- Cell membrane flexibility
- Metabolic potential
- Mitochondrial distribution, morphology, and metabolism
Limitations
- In vitro study (cell culture), limiting direct inference to human health outcomes
- Sample size not reported in the abstract
- Results are described primarily for 24 h exposure; findings for 48 h are not detailed in the abstract
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": 0.05000000000000000277555756156289135105907917022705078125,
"sar_wkg": null,
"duration": "24 and 48 h"
},
"population": "Adipose-derived mesenchymal stem cells (ASCs) in vitro",
"sample_size": null,
"outcomes": [
"N6-methyladenosine (mA) RNA methylation",
"Stem cell marker expression (Nanog, Oct-4, Sox-2, CD44, CD105)",
"Protein levels (p21, DNMT2/TRDMT1, p53)",
"Cell membrane flexibility",
"Metabolic potential",
"Mitochondrial distribution, morphology, and metabolism"
],
"main_findings": "ASCs exposed to 50 Hz, 1.5 mT EMF showed a significant increase in N6-methyladenosine RNA methylation after 24 h. After 24 h exposure, stem cell marker expression increased, p21 and DNMT2/TRDMT1 protein levels were upregulated with no differences in p53 profile, and cell membrane flexibility, metabolic potential, and mitochondrial characteristics were altered.",
"effect_direction": "mixed",
"limitations": [
"In vitro study (cell culture), limiting direct inference to human health outcomes",
"Sample size not reported in the abstract",
"Results are described primarily for 24 h exposure; findings for 48 h are not detailed in the abstract"
],
"evidence_strength": "low",
"confidence": 0.7800000000000000266453525910037569701671600341796875,
"peer_reviewed_likely": "yes",
"keywords": [
"electromagnetic field",
"ELF-EMF",
"50 Hz",
"1.5 mT",
"adipose-derived stem cells",
"mesenchymal stem cells",
"N6-methyladenosine",
"m6A",
"RNA methylation",
"epitranscriptomic changes",
"preconditioning",
"mitochondria",
"metabolic potential",
"p21",
"DNMT2/TRDMT1"
],
"suggested_hubs": []
}
AI can be wrong. Always verify against the paper.
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