Abstract
We investigated whether X-ray radiation induced apoptosis of the proliferative ependymal cells (ECs) in adult rats with spinal cord injury (SCI) and the effect of X-ray radiation on the proliferative activities of ECs. A rat model with SCI was developed and used to determine the proliferation and apoptosis of ECs in the spinal cords after X-ray exposure. TUNEL assay and BrdU incorporation were used to detect apoptosis and proliferation respectively. We found that there were few TUNEL-positive cells in proliferative ependymal zone (EZ) after SCI except at the epicenter, and approximately half of the irradiated ECs became TUNEL-positive. However, these radiated ECs did not lose their proliferative activity until 1 week later and started to decrease rapidly after 1 week. The observation suggested that only part of ECs were sensitive to radiation and the nonsensitive cells continued their mitosis process. These findings indicated that X-ray exposure of the rats with SCI in early stage induced apoptosis of the proliferative ECs and partially inhibited their proliferative activities.
Abbreviations: | ||
SCI | = | spinal cord injury |
NSCs/NPCs | = | neural stem/precursor cells |
ECs | = | ependymal cells |
TUNEL | = | terminal deoxynucleotidy transferase-mediated dUTP nick end labeling |
FITC | = | fluorescein isothiocyanate |
TRITC | = | tetraethyl rhodamine isothiocyanate |
EZ | = | ependymal zone |
PBS | = | phosphate buffered saline |
PB | = | phosphate buffer |
Abbreviations: | ||
SCI | = | spinal cord injury |
NSCs/NPCs | = | neural stem/precursor cells |
ECs | = | ependymal cells |
TUNEL | = | terminal deoxynucleotidy transferase-mediated dUTP nick end labeling |
FITC | = | fluorescein isothiocyanate |
TRITC | = | tetraethyl rhodamine isothiocyanate |
EZ | = | ependymal zone |
PBS | = | phosphate buffered saline |
PB | = | phosphate buffer |