Zhao Feng, Pan Wen, Liang Yan-bing, Tang Hao, Chen Zhi-bin, Lin Miao-xia, Yang Xiao-yan, Zhou Wei-xiong, Ma Zhong-fu
Department of Emergency, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong, China.
Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2007 Oct;19(10):606-9.
To investigate the change in suppressor of cytokine signaling-1 (SOCS1) gene in the liver and the spleen of septic mouse, and to find out its probable mechanisms of action in sepsis.
Cecal ligation and puncture (CLP) was adopted to reproduce sepsis model. The liver and the spleen tissues were harvested and RNA and protein were respectively extracted. The contents of the regulatory genes SOCS1 mRNA were determined by reverse transcription-polymerase chain reaction (RT-PCR) and regulatory content of protein was detected by Western blotting. The SPSS statistics software was adopted to calculate the correlation.
The expressions of SOCS1 on gene and protein in the liver were markedly upregulated at 6 th hour. The gene expression peaked at the 24 th hour (P<0.05).The expression of protein was persistently high. However, the expression of SOCS1 was only detected in the spleen, and it obviously rose in strength with the passage of time, and it remained in a high level. By statistical analysis, positive correlations were found between the gene and protein expressions of SOCS1 (y=0.110+/-5.765 x 10(-3) x, r=0.837, F=93.309, P<0.01).
CLP induced sepsis can induce the up-regulation of the expressions of SOCS1, indicating that SOCS1 play important role in the change in immune system in sepsis. They may be used to intervene sepsis so as to improve the outcome of sepsis.
研究脓毒症小鼠肝脏和脾脏中细胞因子信号转导抑制因子1(SOCS1)基因的变化,探讨其在脓毒症中可能的作用机制。
采用盲肠结扎穿孔术(CLP)复制脓毒症模型。采集肝脏和脾脏组织,分别提取RNA和蛋白质。通过逆转录-聚合酶链反应(RT-PCR)检测调节基因SOCS1 mRNA的含量,采用蛋白质印迹法检测蛋白质的调节含量。采用SPSS统计软件计算相关性。
肝脏中SOCS1基因和蛋白质的表达在第6小时显著上调。基因表达在第24小时达到峰值(P<0.05),蛋白质表达持续处于高水平。然而,SOCS1的表达仅在脾脏中检测到,且随着时间的推移其强度明显升高,并维持在高水平。经统计学分析,SOCS1基因和蛋白质表达之间呈正相关(y=0.110±5.765×10⁻³x,r=0.837,F=93.309,P<0.01)。
CLP诱导的脓毒症可诱导SOCS1表达上调,表明SOCS1在脓毒症免疫系统变化中起重要作用。它们可能用于干预脓毒症,从而改善脓毒症的预后。