Differentially expressed genes identified by microarray analysis following leptin treatment of hepatic stellate cells

被引:0
|
作者
Zhong Li-hua [1 ]
Cheng Jun [2 ]
Zhu Li-ying [1 ]
机构
[1] Harbin Med Coll, Affiliated Hosp 4, Dept Infect Dis, Harbin 150001, Heilongjiang, Peoples R China
[2] Beijing Ditan Hosp, Inst Infect Dis, Beijing 100011, Peoples R China
关键词
leptin; hepatic stellate cells; microarray analysis; SURFACTANT PROTEIN-A; IDIOPATHIC PULMONARY-FIBROSIS; DESATURASE; RAT;
D O I
10.3760/cma.j.issn.0366-6999.2010.06.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Liver fibrosis is the process through which numerous chronic liver diseases develop into liver cirrhosis. Leptin can activate hepatic stellate cells (HSCs) and play an important role in the formation of liver fibrosis. However, the process by which leptin activates HSCs is complicated, and research on this process is limited. The aim of this study was to explore the related changes in gene expression and the control mechanisms involved in leptin activated HSCs to understand the overall mechanism of liver fibrosis development. Methods We cultivate rat HSCs, with and without stimulation by leptin, and extracted mRNA. Differentially expressed genes were detected by microarray analysis. Results The differentially expressed genes identified included six upregulated genes and six downregulated genes. The representative upregulated genes included short chain dehydrogenase (CY5/CY3=2.265) and pulmonary surfactant protein Al (CY5/CY3=2.036). The significant downregulated gene encoded hepatic stearoyl coenzyme A desaturase 1 (SCD-1) (CY5/CY3=0.351). Conclusion Leptin might mediate the molecular biological mechanisms of liver fibrosis. Chin Med J 2010;123(6):726-729
引用
收藏
页码:726 / 729
页数:4
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