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不同状态巨噬细胞对RSC96细胞NGF及Laminin表达的影响

The effects of macrophage in different activation states on NGF and Laminin expressions of RSC96 cells
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摘要 目的研究不同活化状态的巨噬细胞与雪旺细胞株(RSC96)共培养条件下雪旺细胞神经营养因子(NGF)及层粘连蛋白(Laminin,LN)的表达情况。方法利用Transwell建立大鼠腹膜腔巨噬细胞和RSC96细胞的共培养体系,分别将RSC96细胞与未激活巨噬细胞、激活态巨噬细胞共培养;采用Real-time PCR检测、Western blot分析、以及酶联ELISA测定等研究手段,比较各组NGF及LN的表达差异。结果与未激活巨噬细胞共培养组RSC96细胞NGF表达增强,激活态组表达明显增强;而各组LN表达差异不明显。结论巨噬细胞对RSC96细胞NGF表达有促进作用,受其活化状态的影响,激活状态的巨噬细胞的促进作用更明显;对影响RSC96细胞迁移功能的LN的表达作用不明显,无统计学意义,有待进一步研究。 Objective To study the expression of NGF and Laminin in RSC96 cells under co-culture with macrophages in different activation states. Methods A Transwell system was built to co-culture RSC96 cells with rat peritoneal macrophages. Real-time PCR, western blotting, and ELISA were used to detect NGF and LN expression in each group. R0sults Under macrophage co-culture, the NGF expression in RSC96 cells was increased. A significant promotion has been found with activated macrophages. With regard to LN expression, no significant difference was detected. Conclusions The macrophage could contribute to the NGF expression in RSC96 cells, the effect of which is influenced by the activation states. Activated macrophages showed greater effect. No such promotion is found on LN expression, which is associated more with the migration of the Schwann cells. Further research is needed.
出处 《中国临床解剖学杂志》 CSCD 北大核心 2013年第3期321-324,共4页 Chinese Journal of Clinical Anatomy
基金 澳门科学技术发展基金(016-2009-A1)
关键词 RSC96细胞 巨噬细胞 NGF LAMININ 共培养 RSC96 cells Macrophages NGF Laminin co-cultured
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参考文献10

  • 1王国英,胡耀民,钟世镇.巨噬细胞在周围神经损伤和再生中的行为及其作用[J].神经解剖学杂志,1994,10(1):83-88. 被引量:8
  • 2Ydens E, Cauwels A, Asselbergh B, et al. Acute injury in the peripheral nervous system triggers an alternative macrophage response [J]. J Neuroinflammation, 2012, 9:176.
  • 3龚炎培,汤锦波,顾剑辉,丁斐,顾晓松.巨噬细胞对体外培养的雪旺细胞及背根神经节感觉神经元作用的实验研究[J].中华手外科杂志,2005,21(5):311-313. 被引量:5
  • 4Rotshenker S. Wallerian degeneration: the innate-immune response to traumatic nerve injury [J]. J Neuroinflammation,2011,8:109.
  • 5Hai M, Muja N, Devries GH, et al. Comparative analysis of Schwann cell lines as model systems for myelin gene transcription studies [J]. J Neurosci Res, 2002, 69(4):497-508.
  • 6Mcgowan KA, Marinkovich MP. Laminins and human disease [J]. Mierosc Res Tech, 2000, 51 (3):262-279.
  • 7Comejo M, Nambi D, Walheim C, et al. Effect ofNRG1, GDNF, EGF and NGF in the migration of a Sehwann eell precursor line [J]. Neurochem Res, 2010, 35(10): 1643-1651.
  • 8Hoke A, Gordon T, Zochodne DW, et al. A decline in glial cell-line-derived neurotrophic factor expression is associated with impaired regeneration after long-term Schwann cell denervation [J]. Exp Neurol, 2002, 173(1):77-85.
  • 9Kester MH, Kaptein E, Roest TJ, et al. Characterization of rat iodothyronine sulfotransferase s [J]. Am J Physiol Endocrinol Metab, 2003, 285(3):E592-E598.
  • 10Omura T, Omura K, Sano M, et al. Spatiotemporal quantification of recruit and resident macrophages after crush nerve injury utilizing immunohistochemistry [J]. Brain Res, 2005, 1057(1-2):29-36.

二级参考文献5

  • 1Carey DJ, Bunge RP. Factors influencing the releasse of proteins by cultured Schwann cells. J Cell Biol,1981, 91(3ptl):666-672.
  • 2Assouline JG, Bosch P. Lim R, et al. Rat astrocytes and Schwann cells in culture synthesize nerve growth factor-like neurite-promoting factors. Brian Res,1987,428:103-118.
  • 3Lindholm D, Heumann R, Meyer M, et al. Interleukin-1 regulates synthesis of nerve growth factor in non-neuronal cells of rat sciatic nerve. Nature,1987,330:658-659.
  • 4Bolin LM, Shooter EM. Neurons regulate Schwann cell genes by diffusible molecules. J Cell Biol,1993,123:237-243.
  • 5劳杰,姜良福,顾玉东,丁小燕.脑源性神经营养因子在激活态雪旺细胞中表达的初步实验研究[J].中华手外科杂志,2003,19(2):109-111. 被引量:18

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