Cycloheximide stimulates suppressor of cytokine signaling-3 gene expression in 3T3-L1 adipocytes via the extracellular signal-regulated kinase pathway

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题名:	Cycloheximide stimulates suppressor of cytokine signaling-3 gene expression in 3T3-L1 adipocytes via the extracellular signal-regulated kinase pathway
作者:	高永旭;Chang, Hsin-Huei;Tsai, Pei-Hua;Liu, Chi-Wei;Ku, Hui-Chen;Kao, Chung-Cheng;Kao, Yung-Hsi
贡献者:	生醫理工學院生命科學系
关键词:	3T3-L1 Cells;actinomycin D;Adipocytes;Adipocytes, White - drug effects;Adipocytes, White - metabolism;Animals;Cell Line;Cycloheximide;Cycloheximide - pharmacology;Cytokines;Dactinomycin - pharmacology;Down-Regulation - drug effects;energy metabolism;Gene expression;Genes;hormones;Inhibitors;Isoenzymes - genetics;Isoenzymes - metabolism;Kinases;MAP Kinase Signaling System - drug effects;messenger RNA;Mice;Mitogen-activated protein kinase;Osmolar Concentration;Pathways;Protein Kinase Inhibitors - pharmacology;Protein Synthesis Inhibitors - pharmacology;Rats;Regulators;RNA, Messenger - metabolism;SOCS family;SOCS-3;Stimulation;Suppressor of Cytokine Signaling 3 Protein;Suppressor of Cytokine Signaling Proteins - genetics;Suppressor of Cytokine Signaling Proteins - metabolism;Suppressors;Time Factors;Up-Regulation - drug effects
日期:	2013-01-16
上传时间:	2026-04-23 11:12:15 (UTC+8)
出版者:	Netherlands: Elsevier Ireland Ltd
摘要:	摘要： ► Cycloheximide activates adipocyte SOCS-3 gene expression. ► Cycloheximide selectively affects gene expression of other SOCS family members. ► The MEK1/ERK-mediated pathway is necessary for the effect of cycloheximide. ► The effect of cycloheximide on SOCS-3 gene expression varies with the cell type. Suppressor of cytokine signaling (SOCS)-3 can act as a regulator of energy metabolism and cytokine signaling in fat cells. It is regulated by hormones and toxicological factors. However, the action of cycloheximide on expression of adipocyte SOCS-3 gene is unknown. Using 3T3-L1 adipocytes, we found that cycloheximide up-regulated SOCS-3 mRNA expression in dose- and time-dependent manners. Treatment with actinomycin D prevented cycloheximide-stimulated SOCS-3 mRNA expression, suggesting that the effect of cycloheximide requires new mRNA synthesis. While cycloheximide was shown to increase activities of MEK1 and JNK, signaling was demonstrated to be inhibited by pretreatment with either MEK1 inhibitors U0126 and PD98059, or with the JNK inhibitor SP600125. U0126 and PD98059, respectively, reduced cycloheximide-stimulated SOCS-3 mRNA expression, but SP600125 did not antagonize cycloheximide effect. Moreover, cycloheximide was observed to up-regulate expression of other SOCS family members, such as SOCS-1, -2, -4, -5, -6, -7, and cytokine-inducible SH2-containing protein (CIS)-1 mRNAs. Such effects varied with the dosage and duration of cycloheximide treatment. These results imply the functional MEK1/ERK-mediated pathway is necessary for the cycloheximide stimulation of SOCS-3 gene expression. 其他題名： Toxicol Lett 出版者： Netherlands: Elsevier Ireland Ltd 出版日期： 2013-02-13 出處： Toxicology letters, 2013-02, Vol.217 (1), p.42-49 版權： 2012 Elsevier Ireland Ltd 版權： Copyright © 2012 Elsevier Ireland Ltd. All rights reserved. 識別號： ISSN: 0378-4274 識別號： ISSN: 1879-3169 識別號： EISSN: 1879-3169 識別號： DOI: 10.1016/j.toxlet.2012.12.002 識別號： PMID: 23237828
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