期刊文献+

NEP1-40基因修饰的神经干细胞移植对脊髓损伤大鼠行为学恢复的影响 被引量:6

Effect of NEP1-40 Gene Modified Neural Stem Cell Transplantation on the Behavior Recovery of Rats after Spinal Cord Injury
原文传递
导出
摘要 目的通过与单纯的神经干细胞移植进行比较,探讨NEP1-40基因修饰的神经干细胞移植对脊髓损伤大鼠行为学恢复的影响。方法从孕18 d的Sprague-Dawley(SD)大鼠胚胎大脑皮质中分离获得原代神经干细胞,体外培养及传代后采用巢蛋白免疫荧光染色进行鉴定。采用已成功构建的慢病毒载体将NEP1-40基因导入第3代神经干细胞内建立NEP1-40基因修饰的神经干细胞。将30只SD大鼠在第9胸椎水平进行脊髓右侧半切后随机分为3组,每组各10只,伤后第7天在损伤局部分别植入细胞培养液(损伤组)、神经干细胞(NSC组)及NEP1-40基因修饰的神经干细胞(NEP1-40-NSC组)。另取10只仅行第8~10胸椎椎板切除,设置为假手术组。细胞移植前和移植后8周通过Basso-Beattle-Bresnahan(BBB)运动功能评分及网格测试评价神经功能恢复情况。结果细胞移植后8周,BBB测试及网格测试结果显示:损伤组大鼠BBB评分最低且网格摔倒次数最多,单纯神经干细胞移植组BBB评分较之增高且网格摔倒次数减少(P〈0.01),而NEP1-40基因修饰的神经干细胞移植组BBB评分最高且网格摔倒次数最少,和前两组相比差异均有统计学意义(P〈0.01)。结论 NEP1-40基因修饰能进一步提高单纯神经干细胞移植对于大鼠脊髓损伤后行为功能恢复的治疗效果,为研究神经干细胞移植治疗脊髓损伤提供了新的思路和实验依据。 Objective To investigate the behavioral recovery of spinal cord injury(SCI) rats that received transplantation of NEP1-40 gene-modified neural stem cells. Methods Neural stem cells(NSCs) were derived from the cortex tissue of rat embryo at the age of 18 days and identified by Nestin immunofluorescence. The lentiviruses were transduced to NSCs to construct NEP1-40 gene modified NSCs. Spinal cords of 30 Sprague-Dawley rats were hemisected at the nineth thoracic vertebrae level. The rats were randomly assigned to three groups. Cell culture medium, NSCs and NEP1-40 gene-modified NSCs were transplanted into the lesion site of rats of SCI group, NSCs group and NEP1-40-NSCs group respectively 7 days after injury. Additional 10 rats served as blank control group(sham group), which only received laminectomy. Following transplantation, behavior tests including Basso, Beattie, Bresnahan(BBB) Locomotor Rating Scale and grid test were utilized to evaluate spinal cord functional recovery. Results Behavior tests 8 weeks after cells transplantation showed that the rats in SCI group got worst results, the BBB scores improved and the grid drop times reduced significantly in NSCs transplantation group(P 〈 0.01) and behavioral test outcomes were best in the NEP1-40 gene-modified NSCs group(P 〈 0.01). Conclusions NEP1-40 gene modification can significantly improve the behavioral recovery of SCI rats that received transplantation of pure neural stem cells. It can provide a new idea and reliable experimental base for the study of NSCs transplantation for spinal cord injury.
出处 《华西医学》 CAS 2014年第11期2006-2011,共6页 West China Medical Journal
基金 高等学校博士学科点专项科研基金(200806100060)~~
关键词 NEP1-40基因 神经干细胞移植 脊髓损伤 Basso-Beattle-Bresnahan运动功能评分 网格测试 大鼠 NEP1-40 gene Neural stem cell transplantation Spinal cord injury Basso-Beattle-Bresnahan test Grid test Rats
  • 相关文献

参考文献23

  • 1Kabatas S, Teng YD. Potential roles of the neural stem cell in the restoration of the injured spinal cord: review of the literature[J]. Turk Neurosurg, 2010, 20(2): 103-110.
  • 2Steward O, Sharp K, Yee KM, et al. A re-assessment of the effects of a Nogo-66 receptor antagonist on regenerative growth of axons and locomotor recovery after spinal cord injury in mice[J]. Exp Neurol, 2008, 209(2): 446-468.
  • 3Atalay B, Bavbek M, Ozen O, et al. Nogo-A inhibitory peptide (NEP 1-40) increases pan-cadherin expression following mild cortical contusion injury in rats[J]. Turk Neurosurg, 2008, 18(4): 356-365.
  • 4朱薇薇,赵红洋,温天莲,郭爱丽,毕玫荣.缺氧缺血性脑损伤新生大鼠脑Nogo受体水平及NEP1-40的神经保护作用[J].中华儿科杂志,2010,48(2):138-142. 被引量:9
  • 5Wang Q, Gou X, Xiong L, et al. Trans-activator of transcription- mediated delivery of NEP1-40 protein into brain has a neuroprotective effect against focal cerebral ischemic injury via inhibition of neuronal apoptosis[J]. Anesthesiology, 2008, 108(6): 1071-1080.
  • 6袁海峰,宋跃明,刘浩,周春光,孔清泉,刘立岷,龚全.NEP1-40基因慢病毒载体构建及鉴定[J].中国修复重建外科杂志,2012,26(2):177-181. 被引量:2
  • 7Li Y, Zhang WM, Wang TH. Optimal location and time for neural stem cell transplantation into transected rat spinal cord[J]. Cell Mol Neurobiol, 2011, 31 (3): 407-414.
  • 8Mcmahon SS, Albermann S, Rooney GE, et al. Engraftment, migration and differentiation of neural stem cells in the rat spinal cord following contusion injury[J]. Cytotherapy, 2010, 12(3): 313-325.
  • 9Basso DM, Beattie MS, Bresnahan JC. A sensitive and reliable locomotor rating scale for open field testing in rats[J]. J Neurotrauma, 1995, 12(1): 1-21.
  • 10Metz GA, Merkler D, Dietz V, et al. Efficient testing of motor function in spinal cord injured rats[J]. Brain Res, 2000, 883(2): 165-177.

二级参考文献16

  • 1宫福良,王坤正,余鹏博,党晓谦,王春生,时志斌,杨佩.NEP1-40基因克隆及蛋白的原核表达和纯化[J].中国修复重建外科杂志,2006,20(1):9-12. 被引量:4
  • 2Zurn AD, Bandtlow CE. Regeneration failure in the CNS: cellular and molecular mechanisms. Adv Exp Med Biol,2006 ,557 :54-76.
  • 3Zhou C,Li Y,Nanda A,et al. HBO suppresses Nogo-A,Ng-R,or RhoA expression in the cerebral cortex after global ischemia. Biochem Biophys Res Commun ,2003,309:368-376.
  • 4Li S, Strittmatter SM. Delayed systemic Nogo-66 receptor antagonist promotes recovery from spinal cord injury. Neuresci, 2003,23: 4219-4227.
  • 5He Z, Koprivica V. The Nogo signaling pathway for regeneration block. Annu Rev Neuresci,2004,27:341-368.
  • 6Cao Y, Shumsky JS, Sabol MA, et al. Nogo-66 receptor antagonist peptide (NEPI-40) administration promotes functional recovery and axonal growth after lateral funiculus injury in the adult rat. Neurorehabil Neural Repair,2008,22:262-278.
  • 7David S, Fry E J, Lopez-Vales R. Novel roles for Nogo receptor in inflammation and disease. Trends Neuresci ,2008,31:221-226.
  • 8Zheng B, Atwal J, Ho C, et al. Genetic deletion of the Nogo receptor does not reduce neurite inhibition in vitro or promote eorticospinal tract regeneration in vivo. Proc Natl Acad Sci USA, 2005,102 : 1205-1210.
  • 9O'Neill P, Whalley K, Ferretti P. Nogo and Nogo-66 receptor in human and chick : implications for development and regeneration. Dev Dyn,2004, 231:109-121.
  • 10Williams G, Wood A, Williams EJ, et al. Ganglioside inhibition of neurite outgrowth requires Nogo receptor function: identification of interaction sites and development of novel antagonists. J Biol Chem,2008,283 : 16641-16652.

共引文献10

同被引文献48

  • 1刘志刚,熊敏,曾云,余化龙,何宁,王志勇,韩珩,陈森.脑源性神经营养因子基因修饰脂肪间充质干细胞移植对急性脊髓损伤大鼠运动功能的恢复作用[J].湖北医药学院学报,2012,31(5):351-354. 被引量:2
  • 2杨志军,徐如祥.神经干细胞标记及活体示踪的研究现状及前景[J].中华神经医学杂志,2005,4(2):109-114. 被引量:14
  • 3刘学强,杨辉,何家全,宋业纯,邱克军,王彬,吕胜青.hTERT转染神经干细胞端粒酶活性及hTERT mRNA检测[J].第三军医大学学报,2006,28(12):1292-1294. 被引量:7
  • 4Reynolds BA, Weiss S. Generation of neurons and astrocytes from isulated cells of the adult mammalian central nervous system[J]. Science, 1992, 255, 1 707 - 1 710.
  • 5Balducci L, Blasi A, Saldarelli M, et al. Immortalization of hu- man adipose- derived stromal cells: production of cell lines with high growth rate, mesenchymal marker expression and capability to secrete high levels of angiogenic factors[J ]. Stem Cell Research & Therapy, 2014, 63(3) : 113 - 121.
  • 6Y Zhao, D H Lam, J Yang. Targeted suicide gene therapy for glioma using human embryonic stem cell - derived neural stem cells genetically modified by baeuloviral vetctors[J ]. Gene Thera- py, 2012, 19, : 189 - 200.
  • 7H Kosaka, T Ichikawa, K kurozumi, et al. Thrapeutic effect suicide gane- transferred mesenchymal stem cells in a rat model of glioma [J]. Cancer Gene Therapy, 2012,19,572 - 578.
  • 8Antor R, Kordower JH, Maidment NT, et al. Neural- targeted gene therapy for rodent and primate hemiparkinsonism [ J ]. Exp Neurol, 1994, 127,207 - 218.
  • 9Juliane Klose, Ntis Ole Schmidt. Suppression of experimental an-toimmune encephalomyelitis by interleukin- 10 transduced neural stern/progenitor cells[J]. J Neuroflammation, 2013,10 : 117.
  • 10Hyuk Min Kim, Dong Hoon, Hwang V, et al. Ex Vivo VEGF Delivery by Neural Stem Cells Enhances Proliferation of Glial Pro- genitors, Angiogenesis, and Tissue Sparing after Spinal Cord In- jury[J]. PLoS ONE, 2009, 4(3):4 987.

引证文献6

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部