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Exposure to 1950-MHz TD-SCDMA Electromagnetic Fields Affects the Apoptosis of Astrocytes via Caspase-3-Dependent Pathway.

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Liu YX, Tai JL, Li GQ, Zhang ZW, Xue JH, Liu HS, Zhu H, Cheng JD, Liu YL, Li AM, Zhang Y. · 2012

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Exposure to 1950-MHz TD-SCDMA electromagnetic fields damaged mitochondria and induced apoptosis in rat astrocytes, but did not appear to promote tumor formation.

Plain English Summary

Summary written for general audiences

Researchers exposed rat astrocytes and C6 glioma cells to 1950-MHz TD-SCDMA electromagnetic fields for 12, 24, and 48 hours to investigate whether the radiation would alter glial cell biology and act as a tumor-promoting agent. After 48 hours of exposure, mitochondria were damaged and significant apoptosis of astrocytes was induced, with increased expression of bax and a reduced level of bcl-2. Astrocytes did not form tumors in either the control or exposed groups, and exposed C6 glioma cells showed no significant differences in biological features or tumor formation ability compared with unexposed cells.

Why This Matters

The study found that electromagnetic field exposure had differential effects on rat astrocytes and C6 glioma cells. In astrocytes, 48 hours of exposure activated caspase-3, described as a hallmark of apoptosis, alongside changes in the proteins bax and bcl-2. Despite these cellular changes in astrocytes, the researchers noted that their results implied that exposure may not promote tumor formation.

Exposure Details

SAR
5.36 W/kg
Source/Device
1950-MHz TD-SCDMA
Exposure Duration
12, 24 and 48 h

Exposure Context

This study used 5.36 W/kg for SAR (device absorption):

Building Biology guidelines are practitioner-based limits from real-world assessments. BioInitiative Report recommendations are based on peer-reviewed science. Check Your Exposure to compare your own measurements.

Where This Falls on the Concern Scale

Study Exposure Level in ContextStudy Exposure Level in ContextThis study: 5.36 W/kgExtreme Concern - 0.1 W/kgFCC Limit - 1.6 W/kgEffects observed in the Extreme Concern range (Building Biology)This level is 3 times the FCC limit
A logarithmic frequency spectrum from 10 Hz to 100 GHz showing where this study's 1.95 GHz exposure sits relative to common EMF sources.Where This Frequency Sits on the EMF SpectrumELFVLFLF / MFHF / VHFUHFSHFmm10 Hz100 GHzThis study: 1.95 GHzPower lines50/60 Hz5G mm28 GHzLogarithmic scale

Study Details

This study investigated whether EMF radiation would alter the biology of glial cells and act as a tumor-promoting agent.

We exposed rat astrocytes and C6 glioma cells to 1950-MHz TD-SCDMA for 12, 24 and 48 h respectively,...

A 48 h of exposure damaged the mitochondria and induced significant apoptosis of astrocytes. Moreove...

Cite This Study
Liu YX, Tai JL, Li GQ, Zhang ZW, Xue JH, Liu HS, Zhu H, Cheng JD, Liu YL, Li AM, Zhang Y. (2012). Exposure to 1950-MHz TD-SCDMA Electromagnetic Fields Affects the Apoptosis of Astrocytes via Caspase-3-Dependent Pathway. PLoS One. 7(8):e42332, 2012.
Show BibTeX
@article{yx_2012_exposure_to_1950mhz_tdscdma_127,
  author = {Liu YX and Tai JL and Li GQ and Zhang ZW and Xue JH and Liu HS and Zhu H and Cheng JD and Liu YL and Li AM and Zhang Y. },
  title = {Exposure to 1950-MHz TD-SCDMA Electromagnetic Fields Affects the Apoptosis of Astrocytes via Caspase-3-Dependent Pathway.},
  year = {2012},
  
  url = {https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0042332},
}

Quick Questions About This Study

Researchers exposed rat astrocytes and C6 glioma cells to 1950-MHz TD-SCDMA electromagnetic fields for 12, 24, and 48 hours.
After 48 hours, exposure damaged the mitochondria and induced significant apoptosis of astrocytes, with caspase-3 activated and bax increased while bcl-2 was reduced.
Astrocytes did not form tumors in either the control or exposure groups.
Unexposed and exposed C6 glioma cells showed no significant differences in either biological features or tumor formation ability.
The results implied that exposure to 1950-MHz TD-SCDMA electromagnetic fields may not promote tumor formation.