Magnetofection of miR-21 promoted by electromagnetic field and iron oxide nanoparticles via the p38 MAPK pathway contributes to osteogenesis and angiogenesis for intervertebral fusion.
Abstract
BACKGROUND: Magnetofection-mediated gene delivery shows great therapeutic potential through the regulation of the direction and degree of differentiation. Lumbar degenerative disc disease (DDD) is a serious global orthopaedic problem. However, even though intervertebral fusion is the gold standard for the treatment of DDD, its therapeutic effect is unsatisfactory. Here, we described a novel magnetofection system for delivering therapeutic miRNAs to promote osteogenesis and angiogenesis in patients with lumbar DDD. RESULTS: Co-stimulation with electromagnetic field (EMF) and iron oxide nanoparticles (IONPs) enhanced magnetofection efficiency significantly. Moreover, in vitro, magnetofection of miR-21 into bone marrow mesenchymal stem cells (BMSCs) and human umbilical endothelial cells (HUVECs) influenced their cellular behaviour and promoted osteogenesis and angiogenesis. Then, gene-edited seed cells were planted onto polycaprolactone (PCL) and hydroxyapatite (HA) scaffolds (PCL/HA scaffolds) and evolved into the ideal tissue-engineered bone to promote intervertebral fusion. Finally, our results showed that EMF and polyethyleneimine (PEI)@IONPs were enhancing transfection efficiency by activating the p38 MAPK pathway. CONCLUSION: Our findings illustrate that a magnetofection system for delivering miR-21 into BMSCs and HUVECs promoted osteogenesis and angiogenesis in vitro and in vivo and that magnetofection transfection efficiency improved significantly under the co-stimulation of EMF and IONPs. Moreover, it relied on the activation of p38 MAPK pathway. This magnetofection system could be a promising therapeutic approach for various orthopaedic diseases.
AI evidence extraction
Main findings
Co-stimulation with electromagnetic field (EMF) and iron oxide nanoparticles (IONPs) significantly enhanced magnetofection efficiency. Magnetofection of miR-21 into BMSCs and HUVECs promoted osteogenesis and angiogenesis in vitro and in vivo, and the enhanced transfection efficiency under EMF and PEI@IONPs was associated with activation of the p38 MAPK pathway.
Outcomes measured
- Magnetofection/transfection efficiency
- Osteogenesis
- Angiogenesis
- Intervertebral fusion (tissue-engineered bone)
- p38 MAPK pathway activation
Limitations
- EMF exposure parameters (e.g., frequency, intensity, duration) not reported in abstract
- Sample size not reported in abstract
- In vivo model details not reported in abstract
Suggested hubs
-
engineering
(0.78) Study develops an EMF+IONP magnetofection system to enhance gene delivery and tissue-engineered bone formation.
View raw extracted JSON
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"outcomes": [
"Magnetofection/transfection efficiency",
"Osteogenesis",
"Angiogenesis",
"Intervertebral fusion (tissue-engineered bone)",
"p38 MAPK pathway activation"
],
"main_findings": "Co-stimulation with electromagnetic field (EMF) and iron oxide nanoparticles (IONPs) significantly enhanced magnetofection efficiency. Magnetofection of miR-21 into BMSCs and HUVECs promoted osteogenesis and angiogenesis in vitro and in vivo, and the enhanced transfection efficiency under EMF and PEI@IONPs was associated with activation of the p38 MAPK pathway.",
"effect_direction": "benefit",
"limitations": [
"EMF exposure parameters (e.g., frequency, intensity, duration) not reported in abstract",
"Sample size not reported in abstract",
"In vivo model details not reported in abstract"
],
"evidence_strength": "low",
"confidence": 0.66000000000000003108624468950438313186168670654296875,
"peer_reviewed_likely": "yes",
"keywords": [
"magnetofection",
"electromagnetic field",
"iron oxide nanoparticles",
"IONPs",
"PEI@IONPs",
"miR-21",
"BMSCs",
"HUVECs",
"osteogenesis",
"angiogenesis",
"intervertebral fusion",
"p38 MAPK"
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}
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}
AI can be wrong. Always verify against the paper.
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