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胰岛素介导的脉冲电场对细胞信号传递的影响 被引量:3

The Pulsed Electric Field Effect on the Cell Signal Pathway Mediated by Insulin
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摘要 使用胞间信号分子介导方式探究了电磁场生物效应的机制.运用含有脉冲电场处理的胰岛素的培养液培养细胞,使用免疫标记法检测细胞内的酪氨酸磷酸化水平,并用基因芯片检测细胞基因表达水平.结果发现,含有电场处理的胰岛素的培养液培育细胞30 min以后,该组细胞的酪氨酸磷酸化水平比对照组低10.33%,表明胰岛素携带的脉冲电场的信息跨膜传入了细胞内.用该培养液培育细胞68 h后,发现在人类已知的12 000个基因中,有55个基因表达发生极其明显的变化.其中某些基因与胰岛素的胞内信号通路密切相关,另一些基因表达的变化与已经发现的胰岛素介导的脉冲电场对细胞增殖的抑制作用相吻合. Insulin was exposed to a pulsed electric field (PEF) for 0 min or 20 min before being added to the culture medium containing L-02 human hepatocytes. Thirty minutes later, the tyrosine phosphorylation level of the cells for each group was monitored by a flow cytometry. The average fluorescent intensity of the test cell groups decreased by 10. 33% compared with the control groups. After the cells were cultured in the medium with the exposed insulin or the normal insulin for 68 hours, the gene expression levels were measured by using a gene expression chip. The change of fifty-five out of 12 000 gene sequences of the test groups were obvious compared to the controls. The human tyrosine phophatase mRNA showed increases in their expressions. These results suggested that, the intercellular signal molecule such as insulin can be the target of the electromagnetic field, and acts as a signal carrier of the information of PEF, which consequently causes its biological effects.
出处 《华东师范大学学报(自然科学版)》 CAS CSCD 北大核心 2004年第4期56-63,共8页 Journal of East China Normal University(Natural Science)
基金 国家自然科学基金(39870193 50137030)上海市科技发展基金(022312114).
关键词 电磁场生物效应 胰岛素的信号系统 酪氨酸磷酸化 mRNA芯片检测 insulin electromagnetic field signal pathway tyrosine phosphorylation gene expres-sion
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  • 1Zhou Jiliang, Li Changlin, Yao Gengdong, et al. Gene expression of cytokine receptors in HL60 cells exposed to a 50 Hz magnetic field [J]. Bioelectromagnetics, 2002, 23: 339-346.
  • 2Kirka Reinbold, Solomon R Pollack. Serum plays a critical role in modulating [Ca2+ ] of primary culture bone cell exposed to weak ion-resonance magnetic fields [J]. Bioelectromagnetics, 1997, 18:203-214.
  • 3刘旸.视音频素材的编码转换[J].电视字幕.特技与动画,2004,11(7):36-38. 被引量:4
  • 4Christian A Baumann, Alan R. Saltiel spatial compartmentalization of signal transduction in insulin action [J].BioEssays, 2001, 23: 215-222.
  • 5Li P M, Zhang W R, Goldstein B J. Suppression of insulin receptor activation by overexpression of the proteintyrosine phosphatase LAR in hepatoma cells [J]. Cell Signal, 1996, 8: 467-473.
  • 6Kulas D T, Freund G G, Mooney R A. The transmembrane protein-tyrosine phosphatase CD45 is associated withdecreased insulin receptor signaling [J]. J Biol Chem, 1996, 271: 755-760.
  • 7Giang D K, Cravatt B F. A second mamalian N-myristoyltransferase [J]. J Biol Chem, 1998, 273: 6595-6598.
  • 8Dorrestijn J, Bos J L, Van der Zon G C, et al. Changes in the signalling status of the small GTP-binding proteins Rac and Rho do not influence insulin-stimulated hexose transport [J]. Exp Clin Endocrinol Diabetes, 1997, 105:254~262.
  • 9Davis S, Aldrich T H, Jones P F, et al. Isolation of angiopoietin-1, a ligand for the TIE2 receptor, by secretiontrap expression cloning[J]. Cell, 1996, 87: 1161-1169.
  • 10Oemar B S, Werner A, Gamier J M, et al. Human conncetive tissue growth factor is expressed in advanced atherosclerotic lesions [J]. Circulation, 1997, 95: 831-839.

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  • 1Murphy J C, Kaden D A, Warren J, et al. Mutat Res., 1993, 296: 221.
  • 2Feychting M, Forss6n U, Floderus B. Epidemiology, 1997, 8: 384.
  • 3Tang I. I., Sun C X, I.iu H, et al. Colloids Surf. B Biointerfaces, 2007, 57: 209.
  • 4LI Le-jun, DAI Yu-wen, XIA Ruo-hong, et al. Bioelectromagnetics, 2005, 26: 639.
  • 5Yakubovich A V, Solovyov I A, Solovyov A V, et al. Eur. Phys. J. D, 2009, 51. 25.
  • 6Shakhnovich E. Chem. Rev. , 2006, 106: 1559.
  • 7Finkelstein A, Ptitsyn O. Protein Physics A Course of I.ectures. Elsevier Books, Oxford, 2002.
  • 8Prabhu N V, Sharp K A. Ann. Rev. Phys. Chem. , 2005, 56.521.
  • 9Duan Y, Kollman P A. Science, 1998, 282: 740.
  • 10Chen C, Xiao Y, Zhang L. Biophys. J, 2005, 88: 3276.

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