期刊文献+

醛固酮致心肌纤维化相关基因的筛选 被引量:2

Screening for genes associated with cardiac fibrosis induced by aldosterone
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摘要 目的:寻找醛固酮独立致心肌纤维化(MF)的分子。方法:利用差速贴壁法分离培养胎儿心肌成纤维细胞(FCFs);选择3 4代细胞给予醛固酮(ALD)处理8 h、提取各组总RNA,用基因组芯片检测差异表达基因,利用Westernblot和RT-PCR对部分基因表达产物进行验证。结果:ALD处理后表达水平改变的基因共1 519个,其中上调的714个,下调的805个。选择与MF发生机制关系密切的趋化因子(C-C基元)配体7(CCL7)、基质金属蛋白酶26(MMP-26)及白细胞介素31受体α(IL31RA)等基因进行RT-PCR和Westernblot验证,结果与芯片检测一致。结论:利用基因芯片检测出ALD处理后FCFs多种基因表达发生改变,部分基因可能与MF有关。 AIM: To investigate differently expressed genes associated with cardiac fibrosis induced independently by aldosterone. METHODS: Fetal cardiac fibroblasts (FCFs) were isolated and cultured. Total RNA was extracted 8 hours after aldosterone administration. Then gene chips were used to screen these RNA samples, Some of candidate genes were confirmed by RT-PCR and Western blot. RESULTS: Differently expressed 1519 genes were screened. Up-regulated genes were 714 while downregulated genes were 805. The expression of CCL7, MMP-26 and IL31RA was tested by RT-PCR and western blot, the results is identical with those by gene chips. CONCLUSION: Gene chip can efficiently single out differently expressed genes induced dependently by aldosterone in FCFs. CCL7, MMP-26 and IL31RA may be associated with cardiac fibrosis induced by aldosterone.
出处 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2012年第4期350-353,共4页 Chinese Journal of Cellular and Molecular Immunology
基金 国家自然科学基金面上项目(30871065)
关键词 醛固酮 心肌纤维化 基因芯片 aldosterone myocardiac fibrosis gene chip
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参考文献11

  • 1Gandhi MS,Kamalov G,Shahbaz AU,et al.Cellular and molecularpathways to myocardial necrosis and replacement fibrosis[J].HeartFail Rev,2011,16(1):23-34.
  • 2Shafiq MM,Miller AB.Blocking aldosterone in heart failures[J].T-her Adv Cardiovasc Dis,2009,3(5):379-385.
  • 3Bunda S,Liu P,Wang Y,et al.Aldosterone induces elastin produc-tion in cardiac fibroblasts through activation of insulin-like growth fac-tor-I receptors in a mineralocorticoid receptor-independent manner[J].Am J Pathol,2007,171(3):809-819.
  • 4Briet M,Schiffrin EL.Aldosterone:effects on the kidney and cardio-vascular system[J].Nat Rev Nephrol,2010,6(5):261-273.
  • 5Leask A.Potential therapeutic targets for cardiac fibrosis:TGFbeta,angiotensin,endothelin,CCN2,and PDGF,partners in fibroblast ac-tivation[J].Circ Res,2010,106(11):1675-1680.
  • 6谢永进,王升启,陈劲松,伯晓晨,杨静,任艺虹.醛固酮对人胎儿心脏成纤维细胞增殖以及胶原表达的影响[J].细胞与分子免疫学杂志,2011,27(4):386-388. 被引量:19
  • 7Jang MK,Kim JY,Jeoung NH,et al.Oxidized low-density lipopro-teins may induce expression of monocyte chemotactic protein-3 in ath-erosclerotic plaques[J].Biochem Biophys Res Commun,2004,323(3):898-905.
  • 8Maddaluno M,Di Lauro M,Di Pascale A,et al.Monocyte chemotac-tic protein-3 induces human coronary smooth muscle cell proliferation[J].Atherosclerosis,2011,217(1):113-119.
  • 9PirilE,Korpi JT,Korkiamki T,et al.Collagenase-2(MMP-8)and matrilysin-2(MMP-26)expression in human wounds of differentetiologies[J].Wound Repair Regen,2007,15(1):47-57.
  • 10Venereau E,Diveu C,Grimaud L,et al.Definition and character-ization of an inhibitor for interleukin-31[J].J Biol Chem,2010,285(20):14955-14963.

二级参考文献4

共引文献18

同被引文献34

  • 1马笑堃,秦贵军,汪丽,张颖辉,岳欣阁.原发性醛固酮增多症38例临床分析[J].郑州大学学报(医学版),2009,44(2):453-454. 被引量:1
  • 2杜昕,易宗春,戴闺柱.血管紧张素Ⅱ和醛固酮对心脏成纤维细胞Ⅲ型胶原mRNA表达的影响[J].中华老年心脑血管病杂志,2000,2(1):45-47. 被引量:7
  • 3Hansson GK, Hermansson A. The immune system in alherosclerosis[J]. Nat Immunol, 2011, 12(3): 204-12.
  • 4Tsou CL, Peters W, Si Y, ct al. Critical roles for CCR2 and MCP-3in monocyte mobilization from bone marrow and recruitment toinflammatory sites[J]. J Clin Invest, 2007,117(4): 902-9.
  • 5Jang MK, Kim JY, Jeoung NH, et al. Oxidized low-dcnsitylipoproteins May induce expression of monocyte chemotacticprotein-3 in atherosclerotic plaques [J]. Biochem Biophys ResCommun, 2004, 323(3): 898-905.
  • 6Wang X, Li X, Yuc TL, ct al. Expression of monocyte chemotacticprotein-3 mRNA in rat vascular smooth muscle cells and in carotidartery after balloon angioplasty [J]. Biochim Biophys Acta, 2000,1500(1):41-8.
  • 7Maddaluno M, Di Lauro M, Di Pascale A, et al. Monocytechemotactic protein-3 induces human coronary smooth muscle cellproliferationfj]. Atherosclerosis, 2011, 217(1): 113-9.
  • 8Davis J, Crampton SP. Hughes CCW. Isolation of Human Umbi-lical Vein Endothelial Cells (HUVEC)[J ]. J Vis Exp, 2007(3): 183.
  • 9Grciffenberg L, Sokolovic Z, Schnittler HJ, et al. Listeriamonocytogenes-infcctcd human umbilical vein endothelial cells:intemalin-indepcndcnt invasion, intracellular growth, movement,and host cell responses [J]. FEMS Microbiol Lett, 1997, 157(1):163-70.
  • 10Zelvyte I, Dominaitienc R, Crisby M, et al. Modulation ofinflammatory mediators and PPARgamma and NFkappaBexpression by pravastatin in response to lipoproteins in humanmonocytes in ri/ro[J]. Pharmacol Res, 2002, 45(2): 147-54.

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