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转录因子NKx2-5表达在大鼠右心室心肌重塑模型的变化 被引量:1

Expression of homeobox transcription factor NKx2-5 in experimental rat of right ventricular myocardial remodeling
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摘要 目的:观察增加大鼠右心室压力负荷后,右心室心肌重塑与同源盒转录因子NKx2-5表达的变化。方法:注射野百合碱(MCT)制作大鼠肺动脉高压模型,测量大鼠不同时间点肺动脉压和右心室肥厚指数;采用RT-PCR法和Westernblot分析,分别测定右心室心肌NKx2-5及其下游基因心房利钠因子(ANF)的mRNA及蛋白表达。结果:注射MCT后第14天,右室心肌明显肥厚,NKx2-5与ANF的mRNA及蛋白表达亦明显增加,与其呈明显正相关。结论:右心室壁压力负荷增加可作为原发性刺激,使在心脏胚胎发育早期表达的心脏同源盒基因NKx2-5表达增加,NKx2-5在成熟心肌重塑中可能起作用。 Objective:To investigate the expression of the cardiac-specific homeobox transcription factor Nkx2-5 in right heart ventricular remodeling associated with pulmonary hypertension induced by monocrotaline(MCT). Methods:MCT was delivered as a single subcutaneous injection(60 mg/kg) into male Sprague-Dawley rats. The mean pulmonary arterial pressure(mPAP) was measured by right-heart catheterization. The weight ratio of the right heart ventricle(RV) to that of left ventricle and septum weight(LV+S)[RV/(LV + S)] was measured and calculated. RT-PCR and Western blot were used to detecte expression of NKx2-5 and ANF. Results:After 14 days of MCT injection, the right ventricular hypertrophy was found. RV/(LV+SP) of the model group was larger than that of the control group. The expression of NKx2-5 and ANF in right heart ventricular tissue began to increase significantly 14 days after the injection of MCT. Conclusion:The right ventricular pressure overload can evoke increasing of NKx2-5 expression, which will be expressed during cardiac development. This suggests NKx2-5 may play a role in the induction of adult myocardial remodeling.
出处 《南京医科大学学报(自然科学版)》 CAS CSCD 北大核心 2005年第6期367-370,共4页 Journal of Nanjing Medical University(Natural Sciences)
基金 江苏省教育厅立项资助项目(01KJD320028) 南京市卫生局资助项目(YKK0246)
关键词 转录因子NKx2-5 心肌重塑 右室压力负荷 homeobox transcription factor NKx2-5 ventricular remodeling the right ventricular pressure
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参考文献7

  • 1Shiojima I, Komuro I, T Mizuno, et al. molecular cloning and characterization of human cardiac homeobox gene CSX1 [J ]. Circ Res, 1996,79(5) :920-929.
  • 2David L , Shewan M, Jane A, et al. Tenascin synthesis,deposition and isoforms in monocrotaline 2 induced pulmonary hypertensive rat lungs [J]. Am J Hysiol,1996,271 (2) :208-215.
  • 3Jamali M, Rogerson PJ, Wilton S, et al. NKx2-5 activity is essential for cardiomyogenesis [J]. J Biol Chem, 2001,276 (45) :42252-42258.
  • 4Chien KR, Zhu H, Knowlton KU, et al. Transcriptional regulation during cardiac growth and development [J].Annu Rev Physiol, 1993,55 ( 1 ): 77-85.
  • 5Small EM, Krieg PA. Transgenic analysis of the atrialnatriuretic factor(ANF) promoter:NKx2-5 and GATA4 binding sites are required for atrial specific expression of ANF[J]. Dev Biol, 2003,261 ( 1 ): 116-131.
  • 6Cleaver OB, Patterson KD, Krieg PA. Overexpression of the tinman-related genes XNkx-2.5 and XNkx-2.3 in Xenopus embryos results in myocardial hyperplasia [J].Development, 1996,122 ( 11 ) :3549-3556.
  • 7Chen JN, Fishman MC. Zebrafish tinman homolog demarcates the heart field and initiates myocardial differentiation [J]. Development, 1996,122 (12): 3809-3816.

同被引文献15

  • 1W. M. H. Hoogaars,P. Barnett,A. F. M. Moorman,V. M. Christoffels.Cardiovascular development: towards biomedical applicability[J].Cellular and Molecular Life Sciences.2007(6)
  • 2A. Moretti,J. Lam,S. M. Evans,K. -L. Laugwitz.Cardiovascular development: towards biomedical applicability[J].Cellular and Molecular Life Sciences.2007(6)
  • 3Hyun Sook Lee,James M. Gruschus,Tao Zhang,James A. Ferretti.Letter to the Editor: NMR assignments of the DNA-bound human Csx/Nkx2.5 homeodomain and NK2-specific domain[J].Journal of Biomolecular NMR.2005(1)
  • 4Harald B?r,J?rg Kreuzer,Anca Cojoc,Lothar Jahn.Upregulation of embryonic transcription factors in right ventricular hypertrophy[J].Basic Research in Cardiology.2003(5)
  • 5J. I. E. Hoffman.Incidence of congenital heart disease: I. Postnatal incidence[J].Pediatric Cardiology.1995(3)
  • 6Ueyama T,Kasahara H,Ishiwata T,Yamasaki N,Izumo S.Csm, acardiac-specific isoform of the RNA helicase Mov10l1, is regulated by Nkx2.5 in embryonic heart[].Journal of Biological Chemistry.2003
  • 7Yamada Y,Sakurada K,Takeda Y,Gojo S,Umezawa A.Sin- gle-cell-derived mesenchymal stem cells overexpressing Csx/ Nkx2.5 and GATA4 undergo the stochastic cardiomyogenic fate and behave like transient amplifying cells[].Experimental Cell Research.2007
  • 8Zhu W,Shiojima I,Hiroi Y,Zou Y,Akazawa H,Mizuka- mi, M, et al.Functional analyses of three Csx/Nkx-2.5 muta- tions that cause human congenital heart disease[].Journal of Biological Chemistry.2000
  • 9Lee HS,Gruschus JM,Zhang T,Ferretti JA.NMR assign- ments of the DNA-bound human Csx/Nkx2.5 homeodomain and NK2-specific domain[].Journal of Biomolecular NMR.2005
  • 10Ikeda Y,Hiroi Y,Hosoda T,Utsunomiya T,Matsuo S,In- oue J, et al.Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease[].Circulation Journal.2002

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