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胰岛素样生长因子结合蛋白2、4在实验性肝细胞损伤中的表达及意义
引用本文:刘立新,孙凌云,郭晓红,张骞骞. 胰岛素样生长因子结合蛋白2、4在实验性肝细胞损伤中的表达及意义[J]. 中国病理生理杂志, 2009, 25(1): 137-143. DOI: 1000-4718
作者姓名:刘立新  孙凌云  郭晓红  张骞骞
作者单位:山西医科大学 1第一医院科研实验中心, 2肝病研究所,3生理学国家重点学科, 4细胞生理学省部共建教育部重点实验室,山西 太原 030001
基金项目:教育部新世纪优秀人才支持计划,山西省自然科学基金,山西省教育厅青年学术带头人基金 
摘    要:目的:通过观察肿瘤坏死因子α (TNF -α)和转化生长因子β1(TGF-β1)两种细胞因子所致体外培养的肝细胞损伤时胰岛素样生长因子结合蛋白2、4(IGFBP2、IGFBP4)的表达变化,探讨IGFBP2和IGFBP4在肝损伤中的作用机制。方法:对人肝细胞株HL-7702分别给予不同浓度的TNF-α、TGF-β1两种处理因素作用24 h,采用免疫细胞化学染色法观察其IGFBP2和IGFBP4的表达变化,再在相同处理培养条件下用MTT比色法检测两种细胞因子对肝细胞抑制率的影响。根据MTT及预实验结果选择TNF-α 20 μg/L作用于人肝细胞株48h,采用Annexin-Ⅴ/PI双染色流式细胞分析法和TUNEL法检测肝细胞凋亡发生率。结果:与对照组相比,各处理组IGFBP2、IGFBP4的表达均显著增加(P<0.05),其中在TNF-α 20 μg/L组和TGF-β1 4 μg/L组表达最强,且与肝细胞抑制率呈正相关关系(P<0.05 or P<0.01)。TNF-α 20 μg/L处理48 h后肝细胞凋亡率明显增加(P<0.01)。结论:IGFBP2、IGFBP4参与了肝细胞的损伤过程,在TNF-α、TGF-β1介导的肝细胞损伤中具有重要作用。

关 键 词:胰岛素样生长因子结合蛋白质类  肝细胞  肿瘤坏死因子  转化生长因子β  
收稿时间:2007-10-19
修稿时间:2008-03-05

Expression of IGFBP2 and IGFBP4 in hepatocytes with experimental injury
LIU Li-xin,SUN Ling-yun,GUO Xiao-hong,ZHANG Qian-qian. Expression of IGFBP2 and IGFBP4 in hepatocytes with experimental injury[J]. Chinese Journal of Pathophysiology, 2009, 25(1): 137-143. DOI: 1000-4718
Authors:LIU Li-xin  SUN Ling-yun  GUO Xiao-hong  ZHANG Qian-qian
Affiliation:1The Experimental Center of Science and Research, The First Hospital, 2Institute of Hepatopathy, 3National Key Science of Physiology, 4Key Laboratory of Cell Physiology of Ministry of Education, Shanxi Medical University, Taiyuan 030001, China. E-mail:lixinliu6@hotmail.com
Abstract:AIM:To explore the mechanism of IGFBP2 and IGFBP4 in hepatocytes with injury induced by TNF-α and TGF-β1. METHODS:Human hepatocyte line (HL-7702) was cultured in vitro and treated with TNF-α or TGF-β1 for 24 h. The expression of IGFBP2 and IGFBP4 was detected by immunochemistry staining. The inhibition ratio of hepatocytes was detected by MTT assay. HL-7702 was treated with TNF-α at concentration of 20 μg/L for 48 h, then the apoptosis of hepatocytes was detected by both Annexin-V /PI and TUNEL assay. RESULTS:The expression of IGFBP2 and IGFBP4 in TNF-α or TGF-β1 treated groups was significantly higher than that in control group (P<0.05). The positive staining of IGFBP2 and IGFBP4 in TNF-α (20 μg/L) treated groups or TGF-β1 (4 μg/L) treated groups was the strongest among all groups. A positive correlation was found between IGFBP2 or IGFBP4 and inhibitory ratio of hepatocytes (P<0.05 or P<0.01). Compared with normal control group, the percentage of apoptosis markedly increased in TNF-α (20 μg/L) treated group (P<0.01). CONCLUSION:IGFBP2 and IGFBP4 involved in the injury process in hepatocytes, indicating an important role in injury of hepatocytes induced by TNF-α or TGF-β1.
Keywords:Insulin-like growth factor binding proteins  Hepatocytes  Tumor necrosis factor  Transforming growth factor beta
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