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小鼠膜性肾病肾脏中MMP-2的表达及意义

EXPRESSION OF MMP-2 PROTEIN IN KIDNEY OF MICE WITH MEMBRANOUS NEPHROPATHY
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摘要 目的:探讨肾脏MMP-2的表达与膜性肾病发病机制间的关系。方法:把小鼠随机分为膜性肾病模型组和对照组,用免疫组织化学(SABC法)检测肾脏组织中MMP-2的表达,用图像分析系统检测基底膜厚度。结果:模型组和对照组肾脏中均有MMP-2表达,且主要表达在肾小管上皮细胞胞浆中。模型组肾组织中MMP-2表达明显强于对照组(P<0·01),且模型组中MMP-2表达与GBM厚度呈正相关(0·01<P<0·05),对照组MMP-2表达与GBM无相关性(P>0·05)。结论:在MN过程中,肾脏中MMP-2参与了GBM增厚形成的调节机制,提示在MN发病中,细胞外基质(ECM)聚集的同时,可能通过反馈调节机制促使肾脏组织中MMP-2表达上调,从而可能在一定程度上减少ECM的过度堆积。 Objective: To research the relativity between mechanism and MMP- 2 protein expression in mice with membranous nephropathy.Methods: Membranous nephropathy mice animals model were used, and the MMP- 2 protein expression in kidney was assessed by immunohistochemistry and the thicknesses of GBM and TBM were measured. Then the statistical methods were used to compare and analyse the data of MN group and control group. Results: MMP - 2 protein were expressed mainly in renal tubule of MN group and control group. The level of MMP- 2 protein in MN group increased remarkably comparing with control group. In MN group, the expressions of MMP- 2 protein paralleled with the thickness of GBM. And in control group, the expression of MMP - 2 protein were not relative to the thickness of GBM; Conclusion: In MN, the abnormal expressions of MMP - 2 protein were relative to the mechanism of MN, and MMP- 2 may play an important role in preventing the developing of MN.
出处 《现代预防医学》 CAS 北大核心 2006年第10期1758-1760,共3页 Modern Preventive Medicine
基金 泸州医学院科研基金支助课题(NO.04017)
关键词 膜性肾病(MN) ECM MMP-2 小鼠动物模型 Menbranous nephropathy (MN) ECM MMP- 2 Animal Model in Mice
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参考文献7

  • 1冯均才,李有华.基质金属蛋白酶及其抑制剂在肾脏病中的作用[J].中国中西医结合肾病杂志,2001,2(10):617-618. 被引量:8
  • 2Border WA,Ward HJ,Kamil ES,et al.Induction of membranous nephrophathy in rabbits by administration of an exogenous cationic antigen[J].J Clin Invest,1982; 69:451.
  • 3孙兴旺,陈明,曹灵,唐学清,王有模.大鼠早期糖尿病肾小球及肾小管的动态病理变化[J].泸州医学院学报,2000,23(5):364-367. 被引量:10
  • 4陈香美.细胞外基质降解酶系统在肾脏疾病中作用的研究[J].解放军医学杂志,2001,26(12):861-863. 被引量:22
  • 5Akiyama K,Shikata K,Sugimoto H,et al.Changes in serum concentrations of matrix metalloproteinases,tissue inhibitors of metalloproteinases and type Ⅳ collagen in patients with various types of glomerulonephritis[J].Res Commun Mol Pathol Pharmacol.1997 Feb; 95 (2):115-28.
  • 6Urushihara M,Kagami S,Kuhara T,et al.Glomerular distribution and gelatinolytic activity of matrix metalloproteinases in human glomerulonephritis[J].Nephrol Dial Transplant.2002; 17 (7):1189-96.
  • 7Coscigan M,Chambers DA,Boot-Handford RP.Collagen turnover in renal disease[J].Exp Nephrol,1995; 3:114-121.

二级参考文献21

  • 1于德民,吴锐,尹潍,袁咏.实验性链脲佐菌素糖尿病动物模型的研究[J].中国糖尿病杂志,1995,3(2):105-109. 被引量:425
  • 2Cossins J,Dudgeon TJ,Catlin G etal.Identification of MMP-18,a putative novel human matrixmetalloproteinase.Biochem-Biophys-Res-Commun,1996,228(2):494 .
  • 3Migatti P.Extracelluar matrix remodeling by metalloproteinases and plas minogenactivators.Kidney Int,1995,47(suppl 49):12.
  • 4Li L,Arers K,Eisen AZ,et al.Activision of gelatinase A(72KDa type IV collagenase)induced by minensin in normal human fibroblasts.Exp Cell Res,1997,232 :322.
  • 5Parsons SL,Watson SA.Matrix metalloproteinases.Br J Surg,1997,84(2):160 .
  • 6Mattei MG,Roeckel N,Olsen-BR,et al.Genes of the membrane-type matrix metalloproteinase(MT-MMP)gene family,MMP14,MMP15,and MMP16,localize to human chromosomes14,16,and 8,respeetively.Genpmics,1997,15;40(1):168.
  • 7Stolow MA,Bauzon DD,Lij et al.Identification and characterization of a novelcollagenase in Xenopus Laevis:possible roles during frog development.Mol B iolCell,1996,7:1471.
  • 8Lwis MP,Norman JT.Differential response of activated versus non-activat ed renalfibroblasts to tubular epithelial cells:a model of initiation and proge ression offibrosis?Exp Nelhrol,1998,6(2):132.
  • 9Anderson SS,Wu K,Nagase H,et al.Effect of matrix glycation expression o f type IVcollagen,MMP-2,MMP-9 and TIMP-1 by human mesangial cell.Cell Adhes Com mun,1996,4(2):89.
  • 10Schafer L,Lorenz T,Daemmrich J,et al.Role of proteinase in renal hypert rophy andmatrix accumulation.Nephrpl Dial Transplant,1995,10(6):801.

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