TY - JOUR
T1 - Transplantation of rat dental pulp stem cells facilities post-lesion recovery in the somatosensory whisker cortex of male Wistar rats
AU - Sabzalizadeh, Mansoureh
AU - Afarinesh, Mohammad Reza
AU - Esmaeili-Mahani, Saeed
AU - Farsinejad, Alireza
AU - Derakhshani, Ali
AU - Arabzadeh, Ehsan
AU - Sheibani, Vahid
N1 - Publisher Copyright:
© 2021
PY - 2021/8
Y1 - 2021/8
N2 - Damage to somatosensory “barrel” cortex reduces the rats’ behavioral sensitivity in discrimination of tactile stimuli. Here, we examined how transplantation of stem cells into the lesioned barrel cortex can help in recovery of sensory capacities. We induced mechanical lesions in the right barrel cortex area of male rats. Three days after lesioning, rats received one of three transplantation types: un-differentiated dental pulp stem cells (U-DPSCs) or differentiated dental pulp stem cells (D-DPSCs), or cell medium (vehicle). A fourth group of rats were control without any Surgery. For 4 consecutive weeks, starting one week after transplantation, we evaluated the rats’ preference to explore novel textures as a measure of sensory discrimination ability, also measured the expression of glial fibrillary acidic protein (GFAP), Olig 2, nestin, neuronal nuclei (NeuN), brain-derived neurotrophic factor (BDNF) and neuroligin1 by immunohistochemistry and western blotting. Unilateral mechanical lesion decreased the rats’ preferential exploration of novel textures compared to the control group across the 4-week behavioral tests. Following stem cell therapy, the rats’ performance significantly improved at week 2–4 compared to the vehicle group. Compared to the control group, there was a significant decrease in the expression of nestin, NeuN, Olig 2, BDNF, neuroligin1 and a significant increase in the expression of GFAP in the vehicle group. The expression of the neural markers was significantly higher in DPSCs compared with the vehicle group whereas GFAP level was lower in DPSCs compared to vehicle. We found that DPSCs therapy affected a range of neuronal markers in the barrel cortex post lesion, and improved the rats’ recovery for sensory discrimination.
AB - Damage to somatosensory “barrel” cortex reduces the rats’ behavioral sensitivity in discrimination of tactile stimuli. Here, we examined how transplantation of stem cells into the lesioned barrel cortex can help in recovery of sensory capacities. We induced mechanical lesions in the right barrel cortex area of male rats. Three days after lesioning, rats received one of three transplantation types: un-differentiated dental pulp stem cells (U-DPSCs) or differentiated dental pulp stem cells (D-DPSCs), or cell medium (vehicle). A fourth group of rats were control without any Surgery. For 4 consecutive weeks, starting one week after transplantation, we evaluated the rats’ preference to explore novel textures as a measure of sensory discrimination ability, also measured the expression of glial fibrillary acidic protein (GFAP), Olig 2, nestin, neuronal nuclei (NeuN), brain-derived neurotrophic factor (BDNF) and neuroligin1 by immunohistochemistry and western blotting. Unilateral mechanical lesion decreased the rats’ preferential exploration of novel textures compared to the control group across the 4-week behavioral tests. Following stem cell therapy, the rats’ performance significantly improved at week 2–4 compared to the vehicle group. Compared to the control group, there was a significant decrease in the expression of nestin, NeuN, Olig 2, BDNF, neuroligin1 and a significant increase in the expression of GFAP in the vehicle group. The expression of the neural markers was significantly higher in DPSCs compared with the vehicle group whereas GFAP level was lower in DPSCs compared to vehicle. We found that DPSCs therapy affected a range of neuronal markers in the barrel cortex post lesion, and improved the rats’ recovery for sensory discrimination.
KW - Barrel cortex
KW - Dental pulp stem cells
KW - Lesion
KW - Rats
KW - Tactile discrimination
UR - http://www.scopus.com/inward/record.url?scp=85106496271&partnerID=8YFLogxK
U2 - 10.1016/j.brainresbull.2021.04.028
DO - 10.1016/j.brainresbull.2021.04.028
M3 - Article
SN - 0361-9230
VL - 173
SP - 150
EP - 161
JO - Brain Research Bulletin
JF - Brain Research Bulletin
ER -