Background Previously we had successfully tracked adult human neural stem cells （NSCs） labeled with superparamagnetic iron oxide particles （SPIOs） in host human brain after transplantation in vivo non-invasively b...Background Previously we had successfully tracked adult human neural stem cells （NSCs） labeled with superparamagnetic iron oxide particles （SPIOs） in host human brain after transplantation in vivo non-invasively by magnetic resonance imaging （MRI）. However, the function of the transplanted NSCs could not be evaluated by the method. In the study, we applied manganese-enhanced MRI （ME-MRI） to detect NSCs function after implantation in brain of rats with traumatic brain injury （TBI） in vivo. Methods Totally 40 TBI rats were randomly divided into 4 groups with 10 rats in each group. In group 1, the TBI rats did not receive NSCs transplantation. MnCI2＂4H20 was intravenously injected, hyperosmolar mannitol was delivered to disrupt rightside blood brain barrier, and its contralateral forepaw was electrically stimulated. In group 2, the TBI rats received NSCs （labeled with SPIO） transplantation, and the ME-MRI procedure was same to group 1. In group 3, the TBI rats received NSCs （labeled with SPIO） transplantation, and the ME-MRI procedure was same to group 1, but diltiazem was introduced during the electrical stimulation period. In group 4, the TBI rats received phosphate buffered saline （PBS） injection, and the ME-MRI procedure was same to group 1. Results Hyperintense signals were detected by ME-MRI in the cortex areas associated with somatosensory in TBI rats of group 2. These signals, which could not be induced in TBI rats of groups 1 and 4, disappeared when diltiazem was introduced in TBI rats of group 3. Conclusion In this initial study, we mapped implanted NSCs activity and its functional participation within local brain area in TBI rats by ME-MRI technique, paving the way for further pre-clinical research.展开更多
基金This work was supported by grants from the Major State Basic Research Program （No. 2010CB945500, No. 2009CB941100 and No. 2007CB947902）, the National Natural Science Foundation of China （No. 90919002 and No. 30870805）, Shanghai Committee of Science and Technology （No. 08dj140053 and No. 2007Y39） and Postgraduate＇s Research Program of Fudan University （2010）.
文摘Background Previously we had successfully tracked adult human neural stem cells （NSCs） labeled with superparamagnetic iron oxide particles （SPIOs） in host human brain after transplantation in vivo non-invasively by magnetic resonance imaging （MRI）. However, the function of the transplanted NSCs could not be evaluated by the method. In the study, we applied manganese-enhanced MRI （ME-MRI） to detect NSCs function after implantation in brain of rats with traumatic brain injury （TBI） in vivo. Methods Totally 40 TBI rats were randomly divided into 4 groups with 10 rats in each group. In group 1, the TBI rats did not receive NSCs transplantation. MnCI2＂4H20 was intravenously injected, hyperosmolar mannitol was delivered to disrupt rightside blood brain barrier, and its contralateral forepaw was electrically stimulated. In group 2, the TBI rats received NSCs （labeled with SPIO） transplantation, and the ME-MRI procedure was same to group 1. In group 3, the TBI rats received NSCs （labeled with SPIO） transplantation, and the ME-MRI procedure was same to group 1, but diltiazem was introduced during the electrical stimulation period. In group 4, the TBI rats received phosphate buffered saline （PBS） injection, and the ME-MRI procedure was same to group 1. Results Hyperintense signals were detected by ME-MRI in the cortex areas associated with somatosensory in TBI rats of group 2. These signals, which could not be induced in TBI rats of groups 1 and 4, disappeared when diltiazem was introduced in TBI rats of group 3. Conclusion In this initial study, we mapped implanted NSCs activity and its functional participation within local brain area in TBI rats by ME-MRI technique, paving the way for further pre-clinical research.
