作者: Lejun Li , Yuwen Dai , Ruohong Xia , Shude Chen , Denjiang Qiao
DOI: 10.1002/BEM.20156
关键词: Signal transduction 、 Insulin receptor 、 Protein tyrosine phosphatase 、 Tyrosine phosphorylation 、 Receptor 、 Molecular biology 、 In vitro 、 Insulin 、 Intracellular 、 Biology
摘要: Thepurposeofthisstudywastoexaminetheeffectsandthemechanismofapulsedelectricfield(PEF) on insulin and its subsequent mediation of proliferative changes in human hepatocytes vitro. The PEF, the electric field intensity coupled into culture medium, was about 0.7 V/m with a repeating frequency 50 Hz. Insulin solution exposed to PEF for 20 min added culturemediumofhumanhepatocytes.Combiningfluorescencespectroscopy,immunocytochemistry, microarrays, RT-PCR MTT, several important events signaling pathways were investigated, including ligand-receptor binding capacity, intracellular tyrosine phosphorylation level, genetranscription, andcell proliferation.PEFproduceda conformational changeofinsulinmolecule. capacity receptors reduced 87% control level after treatment, average decreased by 11%. expression 55 12000 genes examined modified, an increase phosphatase small GTP-binding protein. Based these results, mechanism isproposedtoexplainthebio-effectsofPEFonhepaticcellproliferationthroughtheinsulinsignaling pathway. Bioelectromagnetics 26, 2005. � 2005 Wiley-Liss, Inc.