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机构地区:[1]Department of Neurosurgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology [2]Department of Neurosurgery, the First Affiliated Hospital of Zhengzhou University
出 处:《Journal of Huazhong University of Science and Technology(Medical Sciences)》2016年第4期548-553,共6页华中科技大学学报(医学英德文版)
基 金:supported by the National Natural Science Foundation of China(No.81371380)
摘 要:Evidence suggested that glycogen synthase kinase-3β(GSK-3β) is involved in Nogo-66 inhibiting axonal regeneration in vitro, but its effect in vivo was poorly understood. We showed that stereotactic injection of sh RNA GSK-3β-adeno associated virus(GSK-3β-AAV) diminished syringomyelia and promoted axonal regeneration after spinal cord injury(SCI), using stereotactic injection of sh RNA GSK-3β-AAV(tested with Western blotting and RT-PCR) into the sensorimotor cortex of rats with SCI and by the detection of biotin dextran amine(BDA)-labeled axonal regeneration. We also determined the right position to inject into the sensorimotor cortex. Our findings consolidate the hypothesis that downregulation of GSK-3β promotes axonal regeneration after SCI.Evidence suggested that glycogen synthase kinase-3β(GSK-3β) is involved in Nogo-66 inhibiting axonal regeneration in vitro, but its effect in vivo was poorly understood. We showed that stereotactic injection of sh RNA GSK-3β-adeno associated virus(GSK-3β-AAV) diminished syringomyelia and promoted axonal regeneration after spinal cord injury(SCI), using stereotactic injection of sh RNA GSK-3β-AAV(tested with Western blotting and RT-PCR) into the sensorimotor cortex of rats with SCI and by the detection of biotin dextran amine(BDA)-labeled axonal regeneration. We also determined the right position to inject into the sensorimotor cortex. Our findings consolidate the hypothesis that downregulation of GSK-3β promotes axonal regeneration after SCI.
关 键 词:NEURITES wound healing protein-serine-threonine kinases myelin proteins
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