ELF EMF induces neural differentiation of hBM-MSCs through regulation of (Zn)-metallothionein-3
Abstract
Overview
This study examines the effects of extremely low-frequency electromagnetic field (ELF EMF) on neural differentiation in human bone marrow-derived mesenchymal cells (hBM-MSCs), with implications for neurodegenerative diseases like Alzheimer's disease (AD).
Findings
- ELF EMF exposure leads to decreased proliferation and enhanced neural-like morphology in hBM-MSCs.
- Significant expression of neuronal markers (β-tubulin3, pleiotrophin, and neurofilament-M at the mRNA level and MAP2 at the protein level) were observed post-exposure.
- There is a decrease in metal-response element-transcription factor 1 and MT3 expression, along with a decreased intracellular Zinc concentration.
- Regulatory mechanism for MT3 was suggested during the neural differentiation process.
- Additionally, upregulation of dihydropyrimidinase-related protein 2 and no change in γ-enolase expression were recorded.
Conclusion
The findings highlight a potential regulatory mechanism involving MT3 during the neural differentiation of hBM-MSCs induced by ELF EMF. These insights are critical for developing new treatments for neurodegenerative diseases.