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首页> 外文期刊>International journal of molecular medicine >Multiple roles of SOCS proteins: Differential expression of SOCS1 and SOCS3 in atherosclerosis
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Multiple roles of SOCS proteins: Differential expression of SOCS1 and SOCS3 in atherosclerosis

机译:SOCS蛋白的多重作用:在动脉粥样硬化中SOCS1和SOCS3的差异表达

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Pro-inflammatory cytokines play a key pathogenic role in atherosclerosis, which are induced by the Janus kinase/signal transducer and activator of transduction (JAK/STAT) pathway. Furthermore, the JAK/STAT pathway is negatively regulated by the suppressor of cytokine signaling (SOCS) proteins. However, the change in SOCS expression levels and the correlation between SOCS expression and cholesterol levels in atherosclerosis is not yet well understood. To this end, a mouse model of atherosclerosis was established using apolipoprotein-deficient (ApoE-/-) mice. The mice were fed either a chow or high-fat diet. The mRNA and protein expression of SOCS1 and SOCS3 in plaque and vessels were determined at different time points. Furthermore, SOCS1 and SOCS3 mRNA expression was detected in the peripheral blood mononuclear cells (PBMCs) obtained from 18?male subjects with no coronary heart disease (non-CHD) population. The expression of SOCS1 in the ApoE-/- mice first increased and then decreased and the high-fat diet accelerated the appearance of the peak; the expression of SOCS3 increased with the increased feeding duration, and this trend was more pronounced in the mice fed the high-fat diet. SOCS1/CD68 and SOCS3/CD68 showed opposite trends in expression with the increased duration of the high-fat diet. Interleukin-6 (IL-6) expression in the main aorta of the ApoE-/- mice fed the high-fat diet also increased with the increased feeding duration. In the non-CHD population, the total serum cholesterol levels positively correlated with SOCS3 mRNA expression in the PBMCs (r=0.433, P=0.012). These results demonstrate the differential expression of SOCS1 and SOCS3 in atherosclerosis and suggest that SOCS3, together with IL-6 may promote the formation and development of atherosclerosis.
机译:促炎细胞因子在动脉粥样硬化中起关键的致病作用,其由Janus激酶/信号转导子和转导激活子(JAK / STAT)途径诱导。此外,JAK / STAT途径受细胞因子信号转导(SOCS)蛋白抑制剂的负调控。然而,动脉粥样硬化中SOCS表达水平的变化以及SOCS表达与胆固醇水平之间的相关性尚未被很好地理解。为此,使用载脂蛋白缺乏(ApoE-/-)小鼠建立了动脉粥样硬化的小鼠模型。给小鼠喂食物或高脂饮食。在不同的时间点测定斑块和血管中SOCS1和SOCS3的mRNA和蛋白表达。此外,在从没有冠心病(非CHD)人群的18位男性受试者获得的外周血单个核细胞(PBMC)中检测到SOCS1和SOCS3 mRNA表达。 ApoE-/-小鼠中SOCS1的表达先升高然后降低,高脂饮食加速了峰值的出现。 SOCS3的表达随进食时间的延长而增加,这种趋势在高脂饮食的小鼠中更为明显。随着高脂饮食时间的延长,SOCS1 / CD68和SOCS3 / CD68显示出相反的表达趋势。高脂饮食喂养的ApoE-/-小鼠主动脉中白介素6(IL-6)的表达也随着喂养时间的延长而增加。在非冠心病人群中,总血清胆固醇水平与PBMC中SOCS3 mRNA表达呈正相关(r = 0.433,P = 0.012)。这些结果证明了SOCS1和SOCS3在动脉粥样硬化中的差异表达,并且表明SOCS3与IL-6一起可以促进动脉粥样硬化的形成和发展。

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