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骨髓基质细胞移植对大鼠脊髓损伤后COX-2基因表达的影响

Effect of bone marrow stromal cells transplantation on expressions of COX-2 gene in rats following spinal cord injury
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摘要 目的观察骨髓基质细胞(bone marrow stromal cells,BMSCs)移植对大鼠脊髓损伤后COX-2 mRNA表达的影响。方法分离培养BMSCs并传代。取Wistar雌性大鼠72只随机分为3组:A组18只(假手术组)、B组27只(细胞培养基对照组)和C组27只(BMSCs组)。B组和C组脊髓损伤后进行DMEM或BMSCs损伤周围区注射。应用RT-PCR法和免疫荧光方法检测损伤脊髓组织内COX-2 mRNA的表达及COX-2蛋白分布情况。结果 COX-2 mRNA在A组大鼠脊髓组织中低水平表达。脊髓损伤移植术后,C组COX-2 mRNA表达水平均显著高于相应时间点的B组(P<0.01)。免疫荧光结果显示,A组COX-2仅表达于脊髓内的血管。脊髓损伤后,B组和C组COX-2表达分布则发生变化,主要见于损伤周围区脊髓内的血管和少数脊髓腹侧灰质内的神经元。结论 BMSCs移植能够增加脊髓损伤后COX-2 mRNA的表达。 Objective To observe the effect of bone marrow stromal cells(BMSCs) transplantation on expression of COX-2 mRNA in rats following spinal cord injury.Methods BMSCs were isolated and secondarily cultured.Male Wistar rats were randomly divided into sham-operated group(group A,n=18),DMEM group(group B,n=27),and BMSCs group(group C,n=27).Rats in groups B and C were injected with BMSCs and DMEM after spinal cord injury.Expression of COX-2 mRNA and distribution of COX-2 protein in rat spinal cord tissue were detected by RT-PCR with immunofluorescence staining.Results The expression level of COX-2 mRNA was lower in group A than in groups B and C,and significantly higher in group C than in group B after BMSCs transplantation(P〈 0.01).Immunofluorescence staining showed that the COX-2 was expressed only in spinal cord blood vessels of group A and mainly expressed in spinal cord blood vessels and in a small number of neurons in ventral gray matter of groups B and C.Conclusion BMSCstransplantation can up-regulate the expression of COX-2 mRNA in rats after spinal cord injury.
出处 《解放军医学院学报》 CAS 2013年第7期764-767,共4页 Academic Journal of Chinese PLA Medical School
基金 辽宁省博士科研启动基金项目(20121096) 辽宁医学院博士及出国进修一年以上教师科研启动基金项目(Y2012B011)~~
关键词 脊髓损伤 骨髓基质细胞 细胞移植 环氧化酶-2 spinal injury bone marrow stromal cells cell transplantation cyclooxygenase-2
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参考文献16

  • 1Pal R,Gopinath C,Rao NM. Functional recovery after transplantation of bone marrow-derived human mesenchymal stromal cells in a rat model of spinal cord injury[J].{H}CYTOTHERAPY,2010,(06):792-806.
  • 2Han X,Yang N,Cui Y. Simvastatin mobilizes bone marrow stromal cells migrating to injured areas and promotes functional recovery after spinal cord injury in the rat[J].{H}Neuroscience Letters,2012,(02):136-141.
  • 3Hammes LS,Tekmal RR,Naud P. Up-regulation of VEGF,c-fms and COX-2 expression correlates with severity of cervical Cancer precursor(CIN)lesions and invasive disease[J].{H}Gynecologic Oncology,2008,(03):445-451.
  • 4Kuwano T,Nakao S,Yamamoto H. Cyclooxygenase 2 is a key enzyme for inflammatory cytokine-induced angiogenesis[J].{H}FASEB JOURNAL,2004,(02):300-310.
  • 5Quertainmont R,Cantinieaux D,Botman O. Mesenchymal stem cell graft improves recovery after spinal cord injury in adult rats through neurotrophic and pro-angiogenic actions[J].PLoS One,2012,(06):e39500.
  • 6Dvoretski?DP,Sokolova IB,Sergeev IV. The effect of intracerebral mesenchymal stem cells transplantation on the density of microvascular network of the pial matter of the rat brain cortex[J].{H}Rossiiskii Fiziologicheskii Zhurnal Imeni I M Sechenova,2012,(04):525-534.
  • 7Nystr?m B,Berglund JE,Bergquist E. Methodological analysis of an experimental spinal cord compression model in the rat[J].{H}Acta Neurologica Scandinavica,1988,(06):460-466.
  • 8Yang H,Chen C. Cyclooxygenase-2 in synaptic signaling[J].{H}Current Pharmaceutical Design,2008,(14):1443-1451.
  • 9Hains BC,Yucra JA,Hulsebosch CE. Reduction of pathological and behavioral deficits following spinal cord contusion injury with the selective cyclooxygenase-2 inhibitor NS-398[J].{H}Journal of Neurotrauma,2001,(04):409-423.
  • 10Aid S,Langenbach R,Bosetti F. Neuroinflammatory response to lipopolysaccharide is exacerbated in mice genetically deficient in cyclooxygenase-2[J].{H}Journal of Neuroinflammation,2008.17.

二级参考文献20

  • 1Pal R, Gopinath C, Rao NM, et al. Functional recovery after transplan- tation of bone marrow-derived human mesenchymal stromal cells in a rat model of spinal cord injury. Cytotherapy, 2010, 12(6): 792-806.
  • 2Ide C, Nakai Y, Nakano N, et al. Bone marrow stromal cell transplanta- tion for treatment of sub-acute spinal cord injury in the rat. Brain Res, 2010, 1332: 32-47.
  • 3Nandoe Tewarie RS, Hurtado A, Bartels RH, et al. Stem cell-based therapies for spinal cord injury. Spinal Cord Med, 2009, 32(2): 105-114.
  • 4Nystrom B, Berglund JE, Bergquist E. Methodological analysis of an experimental spinal cord compression model in the rat. Acta Neurol Scand, 1988, 78(6)" 460-466.
  • 5Weidner N. Intratumor microvessel density as a prognostic factor in cancer. Am J Pathol, 1995, 147(1): 9-19.
  • 6Ritz MF, Graumann U, Gutierrez B, et al. Traumatic spinal cord injury alters angiogenic factors and TGF-Betal that may affect vascular recov- ery. Curr Neurovasc Res, 2010, 7(4): 301-310.
  • 7Herrera JJ, Sundberg LM, Zentilin L, et al. Sustained expression of vascular endothelial growth factor and angiopoietin-1 improves blood spinal cord barrier integrity and functional recovery after spinal cord injury. J Neurotrauma, 2010, 27(11): 2067- 2076.
  • 8Popa C, Popa F, Grigorean VT. Vascular dysfunctions following spinal cord injury. J Med Life, 2010, 3(3): 275-285.
  • 9Tei R, Kaido T, Nakase H, et al. Secondary spinal cord hypoperfusion of circumscribed areas after injury in rats. Neurol Res, 2005, 27(4): 403 -408.
  • 10Widenfalk J, Lipson A, Jubran M, et al. Vascular endothelial growth factor improves functional outcome and decreases secondary degen- eration in experimental spinal cord contusion injury. Neuroscience, 2003, 120(4): 951-960.

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