摘要
肾间质纤维化(renal-interstitial fibrosis,IKIF)是由各种肾脏损害因素导致细胞外基质在肾间质内过度沉积的病理过程,是各种肾脏疾病发展到肾功能衰竭的共同通路和病理基础。因此,研究RIF的发病机制、干预RIF的进程是当前肾脏病界的研究热点。在RIF的各种发生机制中,转化生长因子β(tramforming growth factor~β,TGF~β)过度表达致肾纤维化的作用备受关注。TGF-β在RIF发生过程的多个阶段发挥了重要作用,是肾脏纤维化发生、发展中的关键因子。
出处
《泸州医学院学报》
2008年第6期658-661,共4页
Journal of Luzhou Medical College
参考文献29
-
1Stopa M, Anhuf D, Terstegen L, et al. Participation of Smad2,Smad3 and Smad4 in transforming growth factor-β induced activation of Smad7 [J]. J Biol Chem, 2000; 275 (38):29308
-
2Gersdorff G, Susztak K, Rezvani F, et al. Smad3 and Smad4 mediate transcriptional activation of the human smad7 promoter by transforming growth factor-β[J]. J Biol Chem, 2000;275:11320
-
3Denissova NG, Pouponnot C, Long, et al. Transforming growth factor-β inducible independent binding of SMAD to the Smad7 promoter[J].PNAS, 2000;97:6397
-
4Hanyu A, Ishidou Y, Ebisawa T, et al. The N domain of smad7 is essential for specific inhibition of transforming growth factor-β signaling[J]. J Cell Biol, 2001; 155:1017
-
5Mochizuki T, Miyazaki H, Rezvani F, et al. Role for the MH2 domain of Smad7 in the specific inhibition of transforming growth factor-β superfamily signaling[J].J Biol Chem, 2004; 279:31568
-
6Chen YG, Zhang SP, Fei T, et al. Smad7 antagonizes transforming growth factor β signaling in the nucleus by interfering with functional smad-DNA complex formation [J]. Mol Cell Biol, 2007;27(12):4488
-
7Edlund S, Lee SY, Grimsby S, et al. Interaction between Smad7 and beta-catenin: importance for transforming growth factor beta-induced apoptosis[J].Mol Cell Biol,2005; 25:1475
-
8Shirakihara T, Saitoh M, Miyazono K. Differential regulation of epithelial and mesenchymal markers by δEF1 proteins in epithelial-mesenchymal transition induced by TGF-β[J]. Mol Biol Cell, 2007;18(9):3533
-
9Liu XB, Chen Q, Kuang CZ, et al. A 4.3 kb Smad7 promoter is able to specify gene expression during mouse development[]].Biochim Biophys Acta, 2007; 1769(2): 149
-
10Fukasawa H, Yamamoto T, Togawa A, et al. Down-regulation of Smad7 expression by ubiquitin-dependent degradation contributes to renal fibrosis in obstructive nephropathy in mice[J]. Proc Natl Acad Sci, 2004;101(23):8687
二级参考文献27
-
1Owen WF Jr.Patterns of care for patients with chronic kidney disease in the United States:Dying for improvement[J].J Am Soc Nephrol,2003,14:S76-S80.
-
2Lan HY,Mu W,Tomita N,et al.Inhibition of renal fibrosis by gene transfer of inducible Smad7 using ultrasound-microbubble system in rat UUO model[J].J Am Soc Nephrol,2003,14(6):1 535-1 548.
-
3Datto M,Wang XF.Ubiquitin-mediated degradation a mechanism for fine-turning TGF-beta signaling[J].J Cell,2005,8 121(1):2-4.
-
4Poncelet AC,Schnaper HW.Sp1 and Smad proteins corperate to mediate transforming growth factor-beta 1 induced alpha2 collagen expression in human glomerular mesangial cells[J].J Biol Chem,2001,276(10):6 983-6 992.
-
5Attisano L,Wrana JL.Signal transduction by the TGF-beta superfa-Mily[J].Science,2002,296(5 573):1 646-1 647.
-
6Uchida K,Nitta K,Kobayashi H,et al.Localization of Smad6 and Smad7 in the rat kidney and their regulated expression in the anti-Thy-1 nephritis[J].Cell Biol Res Commun,2000,4(2):98-105.
-
7Ostendorf T,Kunter U,Van Roeyen C,et al.The effects of plated-derived growth Factor antagomism in experimental glomerulonephritis are independent of the transforming growth factor-beta system[J].J Am Soc Nephrol,2002,13(3):658-667.
-
8Fukasawa H,Yamamoto T,Togawa A,et al.Down-regulation of Smad7 expression by ubiquitin-dependent degradation contributes to renal fibrosis in obstructive nephropathy in mice[J].Proc Natl Acad Sci,2004,101(23):8 687-8 692.
-
9Schnaper HW, Hayashida T, Hubchak SC, et al. TGF-beta signal transduction and mesangial cell fibrogenesis. Am J Physiol Renal Physiol, 2003, 284(2) : F243-F252.
-
10Poncelet AC, de Caestecker MP, Schnaper HW. The transforming growth factor-beta/SMAD signaling pathway is present and functional in human mesangial cells. Kidney Int, 1999, 56(4) : 1354-1365.
共引文献33
-
1李乾,张桂英,孟燕妮.氯沙坦对肝纤维化模型鼠Smad2/3,Smad7表达的影响[J].世界华人消化杂志,2004,12(10):2469-2471.
-
2吴晓玲,曾维政,王丕龙.中药干预肝纤维化的分子机制[J].世界华人消化杂志,2004,12(12):2849-2852. 被引量:7
-
3陈樵,曾维政.苦参素抗大鼠肝纤维化作用的实验研究[J].西南军医,2005,7(1):7-9. 被引量:4
-
4曾维政,吴晓玲,蒋明德,王丕龙,褚桂珍.红景天甙对肝纤维化大鼠肝组织CBP、Smad基因表达的影响[J].世界华人消化杂志,2005,13(3):341-345. 被引量:15
-
5梁增文,李德民,张国,王天才.人纤维化肝组织中SMAD蛋白的表达及其意义[J].临床内科杂志,2005,22(9):635-636. 被引量:5
-
6陈莹,郑勇.转化生长因子β_1与肝纤维化的基因治疗[J].胃肠病学和肝病学杂志,2005,14(5):531-533.
-
7梁增文,张国,农兵.人纤维化肝组织中结缔组织生长因子的表达及其意义[J].广东医学,2006,27(5):699-701.
-
8李骢,罗建,湛垚垚,崔小栋,姜妙娜,贾玉杰.中药肝复康对血小板衍化生长因子介导的肝星状细胞信号转导的影响及意义[J].中华消化杂志,2006,26(9):636-638. 被引量:5
-
9梁增文,张国,农兵.结缔组织生长因子在大鼠肝纤维化发生中的作用机制初探[J].陕西医学杂志,2006,35(11):1411-1413.
-
10杨清,关向荣,王星云,柳忠辉.虫草多糖对实验性大鼠Smad2/3 Smad7表达的影响[J].辽宁中医药大学学报,2006,8(6):59-60. 被引量:2
同被引文献3
-
1黄云剑,张远宁,王沂芹,赵景宏,杨唐俊,蔡文琴.PAI-1和TIMP-1基因在肾小管间质纤维化中的表达及HGF的干预作用[J].中国病理生理杂志,2004,20(9):1542-1546. 被引量:18
-
2杨杨,梅长林.KDIGO常染色体显性小管间质性肾病专家共识解读[J].中华肾脏病杂志,2015,31(10):793-796. 被引量:2
-
3毛文丽,崔美玉,张真真,王尊松,张磊,孔祥雷.常染色体显性小管间质性肾病1例并文献复习[J].山东大学学报(医学版),2017,55(2):94-96. 被引量:1
-
1董福兴,万建新.巨噬细胞在肾间质纤维化发生、发展中的作用[J].国际泌尿系统杂志,2016,0(2):302-306.
-
2付广权,张雅芳,杨慧科,刘宝全.TGF-β/Smad信号通路中TGF—β1和Smad7基因在结肠癌中的表达[J].中国中医药咨讯,2010(31):178-179. 被引量:3
-
3陈祯炜,刘垠,肖敏勤,肖鸿,邱炜,赵亚南.过表达Smad7基因对瘢痕疙瘩成纤维细胞的影响[J].中国修复重建外科杂志,2016,30(7):871-875. 被引量:1
-
4贺红焰,何进,李隽,王明勇,刘建.血管紧张素-(1-7)对转化生长因子β1诱导的大鼠肾小球系膜细胞增殖的影响[J].细胞与分子免疫学杂志,2008,24(10):1006-1007.
-
5黄云剑,赵景宏,张憬,范晓棠,张金海,蔡文琴.Smad6和Smad7基因治疗对肾小管间质纤维化进程的影响[J].中华肾脏病杂志,2004,20(5):358-363. 被引量:6
-
6陈颖伟,陈源文,王连升,李定国.Smad7基因过表达对L02肝细胞株增殖的影响[J].上海第二医科大学学报,2005,25(2):103-106. 被引量:1
-
7于鸿,陈琦,刘晔,赵仲华,郭慕依.转染Smad7基因的大鼠肾小球系膜细胞对Ⅰ、Ⅲ型胶原表达的改变[J].复旦学报(医学版),2008,35(3):436-440. 被引量:6
-
8于鸿,王小刚,汪怡,陈琦,张秀荣,郭慕依.转染Smad7基因的大鼠肾系膜细胞uPA及PAI-1表达的改变[J].复旦学报(医学版),2004,31(1):5-8. 被引量:1
-
9Qiang Yan,Weiguo Sui,Shuiyong Xie,Huaizhou Chen,Shenping Xie,Guimina Zou,Hequn Zou.Role of Integrin-linked Kinase (ILK) in Interstitial Fibrosis in Renal Allograft[J].器官移植内科学杂志,2009,4(3):124-133. 被引量:2
-
10张春,朱忠华,刘建社,杨晓,付玲,邓安国.结缔组织生长因子在大鼠肾小管间质纤维化中的表达及意义[J].中华肾脏病杂志,2006,22(2):124-125. 被引量:8