期刊文献+

含M-CSF条件培养液对RAW264.7细胞产生NO的影响 被引量:2

Effect of Macrophage Colony-Stimulating Factor on the Production of Nitric Oxide in RAW264.7 Cells
原文传递
导出
摘要 巨噬细胞集落刺激因子 (M CSF )是一种单核吞噬细胞特异性的生长因子。近年来的研究表明 ,M CSF可以增强巨噬细胞杀伤细菌等病原体及肿瘤细胞的能力 ,对抗感染及抗肿瘤具有重要意义。一氧化氮 (NO )是可由单核吞噬细胞产生的一种自由基 ,对病原体及肿瘤细胞同样具有杀伤作用。为探讨M CSF的抗感染、肿瘤作用是否与其刺激单核吞噬细胞产生NO有关 ,我们以L92 9细胞条件培养液 (L92 9 CM )作为M CSF来源 ,观察了M CSF对巨噬细胞系RAW2 64 7细胞NO产生的影响。结果发现 ,L92 9 CM可以刺激RAW2 64 7细胞NO的产生 ;且RT PCR显示L92 9 CM处理使RAW2 64 7细胞诱导型NO合酶 (iNOS )表达增加。 In order to find out the relationship between the actions of M CSF and NO production of macrophages,we investigated the effect of M CSF on NO production in RAW264 7 cells applying L929 cell conditioned medium (L929 CM) as the source of M CSF The results showed that,L929 CM could increase NO production by RAW264 7 cells Inducible NO synthase (iNOS) mRNA expression was also induced by L929 CM as showed by RT PCR,and the induction could be blocked by cycloheximide
出处 《上海免疫学杂志》 CSCD 北大核心 2000年第4期217-219,共3页 Shanghai Journal of Immunology
基金 国家自然科学基金资助项目 !(编号 39570 867 39670 1 97)
关键词 巨噬细胞集落刺激因子 RAW264.7细胞系 NO macrophage colony-stimulating factor nitric oxide RAW264.7 cell line macrophage
  • 相关文献

参考文献3

二级参考文献2

  • 1雷虹,中国免疫学杂志,1997年,13卷,131页 被引量:1
  • 2曹雪涛,中国免疫学杂志,1994年,10卷,289页 被引量:1

共引文献14

同被引文献17

  • 1Felix R, Hofstetter W, Wellerwald A, et al. Role of colony-stimulating factor-1 in bone metabolism[J]. Cell Biochem,1994,55(3) :340. 被引量:1
  • 2Kimura F, Douzona M, Ohta J, et al. Augmentation of antitumor immunity using genetically M- CSF- expressing L1210 cells[J]. Exp Hematol, 1996,24 : 360-363. 被引量:1
  • 3Sakurai T,Wakimoto N, Yamadam, et al. Effect of macrophage colony-stimulating(M-CSF) on mouse immune responses in vivo[J]. Immunopharmacol Immunotoxicol, 1998, 20 ( 1 ) : 79-102. 被引量:1
  • 4Liu SX, Zhou M, Chen Y, et al. I.opoperoxidative injury to maerophages by oxidatively modified low density lipoprotein may play an important role in foam cell formation[J]. Atherosclerosis, 1996, 121 : 55. 被引量:1
  • 5Wada T,Schwarting A,Chesnutt MS,et al. Nephritogentic cytokines and disease in MRL-Fas(lpr) kidneys are dependent on multiple T-Cell subsets[J]. Kidney Int. 2001,59 (2) : 565-578. 被引量:1
  • 6Moore KJ, Wada T, Barbee SD, Kelley VtL Gene transfer of RANTES elicits autoimmune renal injure in MRL-Fas(lpr)mice[J]. Kidney Int. 1998,53(6) : 1631-1641. 被引量:1
  • 7Schwarting A, Wada T, Kinoshita K, et al. IFN-gamma receptor signaling is essential for the initiation, acceleration, and destruction of autoimmune kidney disease in MRL-Fas( 1 pr)mice[J].Immunol. 1998,161(1) :494-503. 被引量:1
  • 8Bemier T, Halter R, Pau D, et al. M-CSF transgenie mice: role of M-CSF in infection and autoimmune[J]. Exp Toxicol pathol. 2001,53(2-3) : 165-173. 被引量:1
  • 9Rysava R,Merta M,Tesar V, et al. Can serum amyloid A or loid formation process [J]. Biochem Mol Bio Int. 1999,47(5):845-850. 被引量:1
  • 10Campbell IK, Rich MJ, Bischof RJ, et al. The colony- stimulating factors and collagen-induced arthritis: exacerbation of disease by M-CSF and G-CSF and requirement for endogenous M-CSF[J].Leukoc Bio. 2000,68(1) : 144-150. 被引量:1

引证文献2

二级引证文献6

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