Enhanced growth and osteogenic differentiation of Induced Pluripotent Stem cells by Extremely Low-Frequency Electromagnetic Field.
← Research streamCultured iPSCs exposed to pulsed ELF-EMF (50 Hz, 1.5 mT) showed a significantly increased proliferation rate by MTT assay. Osteogenic differentiation measures were significantly increased when cells were cultured under both ELF-EMF and osteogenic medium compa…
Study snapshot
Abstract
It is accepted that induced pluripotent stem cells (iPSCs) have a great osteogenic potential differentiation, in the present study, we tried to improve this potentials using mechanical and biological stimulation. To achieve this goal, the influence of prolonged pulsed extremely low frequency electromagnetic field (ELF—EMF) (50 Hz and 1.5 mT) was investigated on cultured iPSCs. After evaluation of iPSCs biological behavior under radiation using MTT assay, osteogenic differentiation of stem cells was investigated via common important osteogenic markers such as alkaline phosphatase (ALP) activity, calcium mineral deposition and important bone—related genes. MTT result showed that proliferation rate of iPSCs significantly increased followed by stimulate with ELF—EMF. Osteogenic differentiation characterization demonstrated that potential of stem cells also was significantly increased while these cells cultured under both ELF—EMF and osteogenic medium (OM) in comparison to cultured under ELF—EMF or OM alone. According to the results, concluded that combination of OM and ELF—EMF can be a great supplement for bone differentiation of stem cells and appropriate candidate for use in the treatment of bone defects and osteoporosis patients by accelerating healing process.
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
Cultured iPSCs exposed to pulsed ELF-EMF (50 Hz, 1.5 mT) showed a significantly increased proliferation rate by MTT assay. Osteogenic differentiation measures were significantly increased when cells were cultured under both ELF-EMF and osteogenic medium compared with ELF-EMF alone or osteogenic medium alone.
Outcomes measured
- Cell proliferation (MTT assay)
- Osteogenic differentiation markers (alkaline phosphatase activity, calcium mineral deposition)
- Bone-related gene expression
Limitations
- Sample size not reported in the provided abstract/metadata
- Exposure duration details not specified beyond 'prolonged pulsed'
- In vitro study; clinical relevance not established in the provided abstract
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": null,
"sar_wkg": null,
"duration": "prolonged pulsed exposure"
},
"population": "Cultured induced pluripotent stem cells (iPSCs)",
"sample_size": null,
"outcomes": [
"Cell proliferation (MTT assay)",
"Osteogenic differentiation markers (alkaline phosphatase activity, calcium mineral deposition)",
"Bone-related gene expression"
],
"main_findings": "Cultured iPSCs exposed to pulsed ELF-EMF (50 Hz, 1.5 mT) showed a significantly increased proliferation rate by MTT assay. Osteogenic differentiation measures were significantly increased when cells were cultured under both ELF-EMF and osteogenic medium compared with ELF-EMF alone or osteogenic medium alone.",
"effect_direction": "benefit",
"limitations": [
"Sample size not reported in the provided abstract/metadata",
"Exposure duration details not specified beyond 'prolonged pulsed'",
"In vitro study; clinical relevance not established in the provided abstract"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"induced pluripotent stem cells",
"iPSCs",
"extremely low-frequency electromagnetic field",
"ELF-EMF",
"50 Hz",
"1.5 mT",
"pulsed exposure",
"osteogenic differentiation",
"alkaline phosphatase",
"calcium mineral deposition",
"bone-related genes",
"MTT assay"
],
"suggested_hubs": []
}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: Not supplied
PubMed: 25817344
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