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强直性脊柱炎患者TNF-α与MMP-3的相关性
引用本文:杨春花,黄烽. 强直性脊柱炎患者TNF-α与MMP-3的相关性[J]. 军医进修学院学报, 2009, 30(4): 457-459
作者姓名:杨春花  黄烽
作者单位:解放军总医院风湿科,北京,100853
基金项目:留学回国人员科研启动基金 
摘    要:目的研究强直性脊柱炎患者中MMP-3与TNF-α间的作用机制。方法在体外分别分离出5例As患者的外周血单个核细胞(PBMC)和6例As患者的膝关节液中的单个核细胞(SFMC),利用不同浓度人重组MMP-3分别在体外诱导PBMC和SFMC,然后应用ELISA技术检测诱导前后TNF-α度变化;同时在分离了7例脊柱关节病(SpA)患者的PBMC后,又进一步分离出它们的贴壁细胞(adherent cells),研究MMP-3是否选择性地作用于单核-巨噬细胞系统还是淋巴细胞系统。结果不同浓度的MMP-3均能诱导AS患者PBMC释放TNF-α并且TNF-α的浓度具有剂量依赖性;MMP-3能够明显诱导贴壁细胞分泌TNF-α;MMP-3对SFMC具有一定程度的诱导作用,但同时还观察到与PBMC不同的是,即使没有MMP-3的诱导作用,SFMC自身也能分泌一定程度的TNF—α。结论AS患者中,MMP-3与TNF-α之间的相互作用可能是参与其发病的重要原因之一,同时MMP-3可能是通过选择性地作用于AS患者的单核-巨噬细胞系统,而非通过淋巴细胞系统来发挥作用。

关 键 词:脊柱炎,强直性  基质金属蛋白酶  肿瘤坏死因子-α

Correlation between tumor necrosis factor-alpha and matrix metalloproteinase-3 in ankylosing spondylitis patients
YANG Chun-hua,HUANG Feng. Correlation between tumor necrosis factor-alpha and matrix metalloproteinase-3 in ankylosing spondylitis patients[J]. Academic Journal of Pla Postgraduate Medical School, 2009, 30(4): 457-459
Authors:YANG Chun-hua  HUANG Feng
Affiliation:YANG Chun-hua,HUANG Feng Department of Rheumatology,Chinese PLA General Hospital,Beijing 100853,China
Abstract:Objective To study the mechanism of action between matrix metalloproteinase-3 ( MMP-3 ) and tumor necrosis factor-alpha (TNF-α) in ankylosing spondylitis (AS) patients. Methods After peripheral blood mononuclear cells (PBMC) were isolated from 5 AS patients and synovial fluid mononuclear cells (SFMC) were isolated from 6 AS patients with synovial fluids in their knee joints, the PBMC and SFMC were stimulated in vitro with human recombinant MMP-3 and changes in TNF-α expression were detected by enzyme linked immunosorbent assay(ELISA). (Adherent cells were also isolated from PBMC of 7 patients with spondyloarthropathy (SpA) using (human recombinant MMP-3 ) stimulated adherent cells in vitro and the concentration of TNF-α was determined by ELISA). Results Different concentrations of human recombinant MMP-3 induced release of TNF-α by stimulating PBMC in vitro in a dose-dependent manner. The SFMC of AS patients could automatically produce TNF-α even though it was not stimulated by human recombinant MMP-3. Conclusion Interaction between MMP-3 and TNF-α may play an important role in the pathogenesis of AS. MMP-3 may also selectively stimulate monoeytes or maerophages rather than lymphocytes.
Keywords:spondylitis  ankylosing  matrix metalloproteinase 3  tumor necrosis factor-alpha  
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