Electromagnetic fields enhance chondrogenesis of human adipose-derived stem cells in a chondrogenic microenvironment in vitro.
← Research streamPEMF and SPEMF stimulation modules did not cause cytotoxicity or alter cell viability in ADSCs. Both PEMF and SPEMF increased chondrogenic gene expression and sulfated glycosaminoglycan deposition in ADSCs in 2D-HA and 3D-pellet cultures. Bone matrix gene exp…
Study snapshot
Abstract
We tested the hypothesis that electromagnetic field (EMF) stimulation enhances chondrogenesis in human adipose-derived stem cells (ADSCs) in a chondrogenic microenvironment. A two-dimensional hyaluronan (HA)-coated well (2D-HA) and a three-dimensional pellet culture system (3D-pellet) were used as chondrogenic microenvironments. The ADSCs were cultured in 2D-HA or 3D-pellet, and then treated with clinical-use pulse electromagnetic field (PEMF) or the innovative single-pulse electromagnetic field (SPEMF) stimulation. The cytotoxicity, cell viability, and chondrogenic and osteogenic differentiations were analyzed after PEMF or SPEMF treatment. The modules of PEMF and SPEMF stimulations used in this study did not cause cytotoxicity or alter cell viability in ADSCs. Both PEMF and SPEMF enhanced the chondrogenic gene expression (SOX-9, collagen type II, and aggrecan) of ADSCs cultured in 2D-HA and 3D-pellet. The expressions of bone matrix genes (osteocalcin and collagen type I) of ADSCs were not changed after SPEMF treatment in 2D-HA and 3D-pellet; however, they were enhanced by PEMF treatment. Both PEMF and SPEMF increased the cartilaginous matrix (sulfated glycosaminoglycan) deposition of ADSCs. However, PEMF treatment also increased mineralization of ADSCs, but SPEMF treatment did not. Both PEMF and SPEMF enhanced chondrogenic differentiation of ADSCs cultured in a chondrogenic microenvironment. SPEMF treatment enhanced ADSC chondrogenesis, but not osteogenesis, when the cells were cultured in a chondrogenic microenvironment. However, PEMF enhanced both osteogenesis and chondrogenesis under the same conditions. Thus the combination of a chondrogenic microenvironment with SPEMF stimulation can promote chondrogenic differentiation of ADSCs and may be applicable to articular cartilage tissue engineering.
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
PEMF and SPEMF stimulation modules did not cause cytotoxicity or alter cell viability in ADSCs. Both PEMF and SPEMF increased chondrogenic gene expression and sulfated glycosaminoglycan deposition in ADSCs in 2D-HA and 3D-pellet cultures. Bone matrix gene expression and mineralization were increased with PEMF but not with SPEMF.
Outcomes measured
- Cytotoxicity
- Cell viability
- Chondrogenic gene expression (SOX-9, collagen type II, aggrecan)
- Osteogenic/bone matrix gene expression (osteocalcin, collagen type I)
- Cartilaginous matrix deposition (sulfated glycosaminoglycan)
- Mineralization
- Chondrogenic differentiation
- Osteogenic differentiation
Limitations
- No EMF exposure parameters (e.g., frequency, intensity, waveform details, duration) reported in the abstract
- In vitro study; applicability to humans/clinical outcomes not assessed in the abstract
- Sample size not reported in the abstract
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": null,
"source": "clinical-use pulse electromagnetic field (PEMF) and single-pulse electromagnetic field (SPEMF) stimulation",
"frequency_mhz": null,
"sar_wkg": null,
"duration": null
},
"population": "Human adipose-derived stem cells (ADSCs) cultured in chondrogenic microenvironments (2D hyaluronan-coated wells and 3D pellet culture)",
"sample_size": null,
"outcomes": [
"Cytotoxicity",
"Cell viability",
"Chondrogenic gene expression (SOX-9, collagen type II, aggrecan)",
"Osteogenic/bone matrix gene expression (osteocalcin, collagen type I)",
"Cartilaginous matrix deposition (sulfated glycosaminoglycan)",
"Mineralization",
"Chondrogenic differentiation",
"Osteogenic differentiation"
],
"main_findings": "PEMF and SPEMF stimulation modules did not cause cytotoxicity or alter cell viability in ADSCs. Both PEMF and SPEMF increased chondrogenic gene expression and sulfated glycosaminoglycan deposition in ADSCs in 2D-HA and 3D-pellet cultures. Bone matrix gene expression and mineralization were increased with PEMF but not with SPEMF.",
"effect_direction": "benefit",
"limitations": [
"No EMF exposure parameters (e.g., frequency, intensity, waveform details, duration) reported in the abstract",
"In vitro study; applicability to humans/clinical outcomes not assessed in the abstract",
"Sample size not reported in the abstract"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"electromagnetic field",
"PEMF",
"SPEMF",
"adipose-derived stem cells",
"ADSC",
"chondrogenesis",
"osteogenesis",
"hyaluronan",
"pellet culture",
"cartilage tissue engineering",
"sulfated glycosaminoglycan",
"mineralization"
],
"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: 10.1152/japplphysiol.01216.2012
PubMed: 23239875
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