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作 者:王强[1] 余洁[1] 王航[1] 卢巍[1] 邓梦杨[1] 康华利[1] 黄岚[1]
机构地区:[1]第三军医大学新桥医院心血管内科全军心血管病研究所,重庆400037
出 处:《第三军医大学学报》2012年第6期481-484,共4页Journal of Third Military Medical University
基 金:国家自然科学基金(81100112)~~
摘 要:目的观察肝X受体(liver X receptors,LXRs)激动剂T0901317对人脐静脉内皮细胞(human umbilical veinendothelial cell,HUVEC)增殖活性的影响。方法体外分离和培养原代HUVEC,不同浓度的T0901317(0、0.5、2、5μmol/L)干预HUVEC 48 h后,采用MTS法检测HUVEC增殖情况;Western blot检测磷酸化Akt(Ser473)及总Akt的表达。结果T0901317(0~5μmol/L)呈浓度依赖性的促进HUVEC的增殖(P<0.01)和上调HUVEC中p-Akt-Ser473的表达(P<0.01),PI3K抑制剂LY294002(10μmol/L)和基因转录抑制剂放线菌素-D(actinomycin D,Act-D,5μg/ml)可以阻断T0901317(5μmol/L)上调p-Akt-Ser473的作用(P<0.01),提示T0901317通过基因转录调节的方式激活PI3K/Akt信号,此外,PI3K抑制剂LY294002(10μmol/L)预处理可以逆转T0901317(5μmol/L)促HUVEC增殖作用(P<0.01)。结论 LXRs激动剂T0901317可通过激活PI3K/Akt信号通路增强HUVEC的增殖能力。Objective To observe the effect of liver X receptors(LXRs) agonist T0901317 on human umbilical vein endothelial cells(HUVECs) proliferation.Methods The HUVECs isolated and cultured in vitro were treated with different concentrations of T0901317(0,0.5,2 and 5 μmol/L) for 48 h.The proliferation of HUVECs was evaluated by MTS assay.The expressions of phospho-Akt(Ser473) and total Akt were detected by Western blotting.Results The HUVEC proliferation was significantly promoted and the phospho-Akt(Ser473) expression was significantly upregulated by T0901317 in a dose-dependent manner(P0.01).The upregulation of phospho-Akt(Ser473) induced by T0901317 could be blocked by PI3K inhibitor LY294002(10 μmol/L) and gene transcription inhibitor actinomycin D(Act-D)(5 μg/ml)(P0.01),indicating T0901317 activated PI3K/Akt pathway through regulating gene transcription.Moreover,pretreatment of HUVECs with LY294002(10 μmol/L) could reverse T0901317-induced HUVEC proliferation(P0.01).Conclusion The LXRs agonist T0901317 can promote HUVEC proliferation through the activation of PI3K/Akt pathway.
关 键 词:肝X受体 人脐静脉内皮细胞 细胞增殖 PI3K/AKT信号通路
分 类 号:R322.123[医药卫生—人体解剖和组织胚胎学] R329.26[医药卫生—基础医学]
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