期刊文献+

γ干扰素对肾小球肾炎大鼠肾组织Smad7和Ⅳ型胶原mRNA表达的影响 被引量:2

Effects of IFN-γ on the expression of Smad7 and Col Ⅳ in renal tissue of rat with glomerulonephritis
下载PDF
导出
摘要 目的:研究IFN-γ对Thy1肾炎模型大鼠肾组织Sm ad7及Ⅳ型胶原表达的影响,从而为阐明IFN-γ抗肾纤维化机制及治疗肾纤维化提供理论和实验依据。方法:制备大鼠抗胸腺细胞血清(antithymocyte serum,ATS)肾炎模型,经尾静脉一次注射IFN-γ15万IU/kg,采用Northern b lot及免疫组化检测病变肾组织Sm ad7、Ⅳ型胶原的表达水平。结果:注射IFN-γ的ATS肾炎模型大鼠肾组织内Sm ad7的表达增加,Ⅳ型胶原mRNA的表达明显减少。结论:IFN-γ可能是通过上调Sm ad7表达而抑制肾组织Ⅳ型胶原表达的机制,对肾小球纤维化起抑制作用。 Objective: To investigate the mechanism of IFN-γ antifibrosis and provide value clues for searching and developing new approaches to the prevention and treatment of organfibrosis,the expression of Smad7 and type Ⅳ collagen was detected in renal tissue of rat ATS glomerulonephritis.Methods: Rat antithymocyte serum glomerulonephritis model was built successfully adopting injection of IFN-γ 15×104 IU/kg vie tail vein once time.Northern blot and immunohistochemistry were employed to identify protein and mRNA expression of Smad7 and type Ⅳ collagen(Col Ⅳ) in renal tissue of rat ATS glomerulonephritis,respectively.Results: IFN-γ could increase the expression of Smad7 and decrease the expression of Col Ⅳ in renal tissue of rat ATS glomerulonephritis.Conclusion: It is possible that IFN-γ can alleviate the development of glomeruli fibrosis by the mechanism of upregulating the expression of Smad7,then downregulating the expression of Col Ⅳ.
出处 《江苏大学学报(医学版)》 CAS 2011年第2期143-146,F0003,共5页 Journal of Jiangsu University:Medicine Edition
基金 上海市科委发展基金重点资助项目(01JC14018) 泰州市311工程人才基金资助项目(201036)
关键词 系膜细胞 Γ干扰素 SMAD7 Ⅳ型胶原 信号转导 肾小球肾炎 mesangial cell interferon-γ Smad7 type Ⅳ collagen signal transduction glomerulonephritis
  • 相关文献

参考文献15

  • 1Pozzi A, Voziyan PA, Hudson BG, et al. Regulation of matrix synthesis, remodeling and accumulation in' glo- merulosclerosis [ J ]. Curr Pharm Des, 2009, 15 ( 12 ) : 1318 - 1333.
  • 2Yan X, Liu Z, Chen Y. Regulation of TGF-beta signa- ling by Smad7 [ J ]. Acta Biochim Biophy Sin, 2009,41 (4) :263 -472.
  • 3Lan HY, Mu W, Tomita N, et, al. Inhibition of renal fibrosis by gene transfer of inducible Smad7 using ultra- sound-microbubble system in rat UUO model[ J]. J Am Soc Nephml,2003,14(6) : 1535 - 1548.
  • 4Mozes E, Sharabi A. A novel tolerogenic peptide, hCDR1,for the specific treatment of systemic lupus ery- thematosus [ J ]. Autoimmun Rev,2010,10 ( 1 ) :22 - 26.
  • 5Yan X, Chen YG. Smad7 : not only a regulator, but also a cross-talk mediator of TGF-β signaling [ J ]. Biochem J,2011,434(1) :1 - 10.
  • 6Xu JH, Qiu W, Wang YW, et al. Gene expression profile and overexpression of apoptosis-related genes ( NGFI-B and Gadd 45 gamma) in early phase of Thy-1 nephritis model [ J ]. Cell Tissue Res, 2006, 326 ( 1 ) : 159 - 168.
  • 7Rogliani P, Mura M, Assunta Porretta M, et al. New perspectives in the treatment of idiopathic pulmonary fibrosis[J]. Ther Adv Respir Dis,2008,2(2) :75 -93.
  • 8Pockros PJ. Antifibrotics for chronic hepatitis C [ J ]. Clin Liver Dis,2009,13 ( 3 ) : 365 - 373.
  • 9Foster W, Li Y, Usas A,et al. Gamma interferon as an antifibrosis agent in skeletal muscle[ J]. J Orthop Res, 2003,21 (5) :798 - 804.
  • 10Oldroyd SD, Thomas GL, Gabbiani G, et al. Interferon- γ inhibits experimental renal fibrosis [ J ]. Kidney Int, 1999,56(6) :2116-2127.

同被引文献23

  • 1冯凤仪,邓燕,李超雄,李恩华,谈柏浓.扁桃体切除治疗儿童IgA肾病的疗效观察[J].中国医师杂志,2006,8(9):1242-1242. 被引量:7
  • 2杨森,陈双峰,刘伟,耿迎春,孙新中.扁桃体摘除术对IgA肾病患者免疫功能的影响[J].山东医药,2007,47(17):53-54. 被引量:3
  • 3Ebihara I, Hirayama K, Yamamoto S, et al. Th2 predominance at the single-cell level in patients with IgA nephropathy[ J]. Nephrol Dial Transplant,2001,16(9) :1783 - 1789.
  • 4Mum K, Yamagata K, Kobayashi M, et al. Usage of T cell receptor variable segments of the beta-chain in IgA nephropathy [ J ]. Neph- ron,2002,92( 1 ) :56 - 63.
  • 5Lee SM, Rao VM, Franklin WA, et al. IgA Nephropathy: Morphologic Predictors of Progressive Renal Disease [ J ]. Hum Pathol, 1982, 13(4) :314 -322.
  • 6Ebihara I, Hirayama K, Yamamoto S, et al. Th2 predominance at the single-cell level in patients with lgA nephropathy [ J ]. Nephrel Dial Transplant,2001,16 (9) : 1783 - 1789.
  • 7Yano N, Endoh M, Takemura F, et al. Involvement of interleukin-4- and soluble CD23 in hypersynthesis of immunoglobulins A and E in patients with lgA nephropathy[ J]. Nephron, 1996,72 ( 1 ) :44 - 51.
  • 8Ichinose H, Miyazaki M, Koji T, et al. Detection of cytokine mRNA- expressing cells in peripheral blood of patients with lgA nephropathy using non-radioactive in situ hybridization [ J ]. Clin Exp Immunol, 1996,103 ( 1 ) : 125 - 132.
  • 9Suzuki H, Suzuki Y, Aizawa M, et al. Thl polarization in murine IgA nephropathy directed by bone marrow-derived cells [ J]. Kidney Int, 2007,72(3) :319 -327.
  • 10Masutani K, Miyake K, Nakashima H, et al. Impact of interferon-3, and interleukin-4 polymorphisms on development and progression of IgA nephropathy in Japanese patients [ J ]. Am J Kidney Dis, 2003, 41(27 :E371 -379.

引证文献2

二级引证文献7

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