Zuo Yu-Chao, Xiong Nan-Xiang, Zhao Hong-Yang
Department of Neurosurgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Department of Neurosurgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.
J Huazhong Univ Sci Technolog Med Sci. 2016 Aug;36(4):548-553. doi: 10.1007/s11596-016-1623-6. Epub 2016 Jul 28.
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 shRNA GSK-3β-adeno associated virus (GSK-3β-AAV) diminished syringomyelia and promoted axonal regeneration after spinal cord injury (SCI), using stereotactic injection of shRNA 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.
有证据表明,糖原合酶激酶-3β(GSK-3β)参与体外Nogo-66抑制轴突再生,但对其体内作用了解甚少。我们发现,立体定向注射shRNA GSK-3β腺相关病毒(GSK-3β-AAV)可减轻脊髓空洞症,并促进脊髓损伤(SCI)后的轴突再生,方法是将shRNA GSK-3β-AAV立体定向注射到SCI大鼠的感觉运动皮层(通过蛋白质免疫印迹法和逆转录-聚合酶链反应检测),并检测生物素葡聚糖胺(BDA)标记的轴突再生。我们还确定了向感觉运动皮层注射的正确位置。我们的研究结果支持了以下假设,即GSK-3β的下调可促进SCI后的轴突再生。