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siRNA对神经肽Y诱导的大鼠心肌细胞肥大Ca^(2+)/CaM-CaN通路的影响

Effect of siRNA on Ca^(2+)/CaM-CaN Channel in theHypertrophy of Rat Myocyte Stimulated by Neuropeptide Y
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摘要 采用差速贴壁法体外原代培养大鼠心肌细胞;NPY刺激培养的心肌细胞增殖;RNA干涉特异性抑制CaN的活性,阻断NPY刺激的心肌细胞中Ca2+/CaM-CaN信号转导通路;观察对CaN活性、表达水平和心肌细胞蛋白合成速率的变化.实验结果显示NPY可增加心肌细胞的CaN活性和表达,加快细胞内蛋白合成速率.RNA干涉抑制CaN活性后,明显降低NPY刺激的蛋白合成速率.CaN参与了NPY刺激的心肌细胞增殖,RNA干涉通过抑制CaN的活性可阻断N PY诱导的心肌细胞肥大Ca2+/CaM-CaN通路. To investigate the effects of Ca^2+/CaM-dependent calcineurin (CAN) signaling pathway on cardiomyocytes hypertrophy of rat induced by neuropeptide Y (NPY), and the inhibition of siRNA on the activity of CaN and synthesis of cardiomyocytes protein. Cardiomyocytes of neonatal Wistar rats were cultured with 100 nmol/L NPY, RNA interference (RNAi) was used to block CaN-depended signal transduction pathway in rat cardiomyocytes stimulated by NPY, then the activity and the expression level of CaN, proliferation of cardionlyocytes were observed. Results showed that NPY could increase CaN activity and the proliferation of cardiomyocytes. While RNAi inhibited the activity of CaN and cardiomyocytes proliferation. Neumpeptide Y activates Ca^2+/CaM-dependent calcineurin signal pathway, while the activity of CaN and cardiomyocyes proliferation stimulated by NPY could be blocked by RNAi.
出处 《生命科学研究》 CAS CSCD 2006年第3期224-227,共4页 Life Science Research
关键词 RNA干涉 神经肽Y 钙调神经磷酸酶 心肌细胞 RNA interference neuropeptide Y calcineurin cardiomyocytes
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参考文献14

  • 1KLEE C B. REN H,WANG X. Regulation of the calmodulin-stimulated protein phosphatase, calcineurin[J] .J Biol Cheln. 1998. 273(22): 13367-13370.
  • 2VEGA R B. YANG J, ROTHERMEL B A. et al. Multiple domains of MCIP1 contribute to inhibition of calcineurin activity[J].J Biol Chem, 2002. 277(33): 30401-30407.
  • 3SAYEN M R. GUSTAFSSON A B, SUSSMAN M A. et al.Calcineurin transgenic mice have mitochondrial dvsfunction and elevated superoxide production[J]. Am J Physiol Cell Physiol, 2003, 284(2): C562-570.
  • 4MICHALAK M. LYNCH J, GROENENDYK J. et al. Calreticulin in cardiac development and palhology[J]. Biochim Biophys Acta, 2002, 1600( 1-2): 32-37.
  • 5HILL J A. ROTHERMEL B. YOO K D. et al. Targeted inhibition of calcineurin in pressure-overload cardiac hypertrophy. Preservation of systolic function[J]. J Biol Chem. 2002.277(12):10251-10255.
  • 6GUO S. KEMPHUES K J. Par-1. a gene required for estahlishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed[J]. Cell.1995, 81 (4): 611-620.
  • 7FIRE A, XU S. MONTGOMERY M K, et al. Potent and specific genetic interference bv. double-stranded RNA in Caenorhabditis elegans[J] . Nature. 1998. 391 (6669):744-745.
  • 8MAHANTHAPPA N. Translating RNA interference into therapies for human disease [ J ]. Pharmacogenomics. 2005. 6 (8) :879-883.
  • 9HEFTI M A, HARDER B A. EPPENBERGER H M. et al. Signaling pathways in cardiac mvocvte hypertrophy[J]. J Mol Cell Cardiol, 1997, 29: 2873-2892..
  • 10OLSON E N, MOLKEMIN J D. Prevention of cardiac hypertrophy by caleineurin inhibition: hope or hype? [J] . Cire Res. 1999. 84(6): 623-632.

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