期刊文献+

大鼠脊髓损伤后炎症细胞趋化因子MCP-1的表达及其意义 被引量:8

Expression of chemokine MCP 1in rats with spinal cord injury
暂未订购
导出
摘要 目的 :探讨炎症细胞趋化因子单核细胞趋化蛋白 1 (MCP- 1 )在脊髓损伤早期的表达变化及其在脊髓继发性损伤炎症免疫反应中的作用机制。方法 :采用改良 Nystrom法制备大鼠胸段脊髓后路压迫损伤模型 ,运用 RT- PCR技术检测脊髓损伤后 6 h的 MCP- 1 m RNA的表达水平 ,免疫组化方法检测损伤后 3、6、1 2 h和 1、3、5、7d各个时间段 MCP- 1阳性细胞与损伤局部单核 /巨噬细胞数目的变化。 结果 :脊髓损伤后 ,MCP- 1 m RNA水平明显升高 ,MCP- 1阳性细胞高峰时间出现在脊髓损伤后 1 2 h至 3d,同时 ,单核 /巨噬细胞高峰时间出现在损伤后 3~ 7d。 结论 :MCP- 1、单核 /巨噬细胞均参与了脊髓损伤后早期的继发反应 ,单核 /巨噬细胞出现的高峰时间滞后于 MCP- Objective:To study the expression level of MCP-1mRNA after spinal cord injury(SCI)and its role in the secondary immunoreaction at the early stage after SCI.Methods:The animal model of Nystro m's posterior compression in spinal cord was adopted in this study.The expression level of MCP-1mRNA was detedted by RT-PCR on6h post-injury.The expression and distribution of MCP-1positive cells and the infiltration of monocytes/macrophages were measured by im-munohistochemistry on3h,6h,12h,1d,3d,5d,7d post-injury.Results:The level of MCP-1expression significantly in-creased after SCI and the peak MCP-1positive cells appeared at the early period after SCI(12h-3d post-injury),while the peaks of monocytes/macrophages ocurred3-7d post-injury.Conclusion:Both MCP-1and monocyte/macrophage take part in the secondary immunoreaction at the early stage after SCI.In the local injury site,the peak of monocytes/macrophages lags behind that of MCP-1positive cells.
出处 《第二军医大学学报》 CAS CSCD 北大核心 2004年第7期766-768,共3页 Academic Journal of Second Military Medical University
关键词 脊髓损伤 趋化因子 MCP-1 单核 巨噬细胞 spinal cord injury chemokine MCP-1 monocyte/macrophage
  • 相关文献

参考文献9

  • 1Nystrm B,Berglund JE,Bergquist E.Methodological analysis of an experimental spinal cord compression model in the rat[J].Acta Neurol Scand,1988,78(6):460-466.
  • 2Lee YL,Shih K,Bao P,et al.Cytokine chemokine expression in contused rat spinal cord[J].Neurochem Int,2000,36(4-5):417-425.
  • 3Weiss JM,Downie SA,Lyman WD,et al.Astrocyte-derived monocyte chemoattractant protein-1 directs the transmigration of leukocytes across a model of the human blood-brain barrier[J].Immunology,1998,161(12):6896-6903.
  • 4Ghirnikar RS,Lee YL,Eng LF,et al.Inflammation in traumatic brain injury:role of cytokine and chemokines[J].Neurochem Res,1998,23(3):329-340.
  • 5Ma M,Wei T,Boring L,et al.Monocyte recruitment and myelin removal are delayed following spinal cord injury in mice with CCRz chemokine receptor deletion[J].J Neurosci Res,2002,68(6):691-702.
  • 6DeGraba TJ.The role of inflammation after acute stroke:utility of pursuing anti-adhesion molecule therapy[J].Neurology,1998,51(Suppl 3):62-68.
  • 7Ghirnikar RS,Lee YL,Eng LF.Chemokine antagonist infusion attenuates cellular infiltration after spinal cord contusion injury in rat[J].J Neurosci Res,2000,59(1):63-73.
  • 8Popovich PG,Guan Z,Wei P,et al.Depletion of hematogenous macrophages promotes partial hindlimb recovery and neuroanatomical repair after experimental spinal cord injury[J].Exp Neurol,1999,158(2):351-365.
  • 9廖维宏,张光铂.进一步加强脊髓损伤修复研究[J].中国脊柱脊髓杂志,2003,13(9):517-519. 被引量:22

共引文献21

同被引文献110

引证文献8

二级引证文献25

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