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重庆医科大学基础医学院病理学教研室分子医学与肿瘤研究中心
纸质出版日期:2011,
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[1]文雪,易永芬,邓玮,闫田静,屈玉玲.p115和MIF在肝癌细胞和正常肝细胞的表达情况[J].重庆医科大学学报,2011,36(02):136-140.
WEN Xue, et al. A comparative study of p115 and MIF in different hepatocellular carcinoma cell lines and a normal human hepatic cell line[J]. Journal of Chongqing Medical University, 2011,36(2):136-140.
[1]文雪,易永芬,邓玮,闫田静,屈玉玲.p115和MIF在肝癌细胞和正常肝细胞的表达情况[J].重庆医科大学学报,2011,36(02):136-140. DOI: 10.13406/j.cnki.cyxb.2011.02.030.
WEN Xue, et al. A comparative study of p115 and MIF in different hepatocellular carcinoma cell lines and a normal human hepatic cell line[J]. Journal of Chongqing Medical University, 2011,36(2):136-140. DOI: 10.13406/j.cnki.cyxb.2011.02.030.
目的:研究人肝癌低分化SMCC-7721细胞株
高分化HepG2细胞株和人正常肝细胞株LO2的高尔基体转运蛋白p115和巨噬细胞移动抑制因子(Macrophage migration inhibitoryfactor
MIF)的表达情况。方法:采用RT-PCR方法检测3组细胞株中p115和MIF的mRNA表达水平。用Western blot方法和细胞免疫组化方法检测3组细胞株中p115和MIF的蛋白表达情况。结果:SMCC-7721
HepG2的p115和MIF mRNA表达和蛋白表达水平明显增加且SMCC-7721表达更强
与对照组正常肝细胞株LO2的表达量比较有显著差异(P<0.05);细胞免疫组化方法结果显示:SMCC-7721
HepG2中p115在主要位于除高尔基体外的细胞质中
但在细胞质中HepG2着色相对较淡
而LO2中位于细胞核旁的高尔基体上。MIF主要分布于细胞质中
其在SMCC-7721、HepG2、LO23组细胞表达量呈明显减弱
统计学有显著差异(P<0.05)。结论:p115和MIF的含量在SMCC-7721、HepG2、LO2 3组细胞株中呈递减性变化。说明随着细胞恶性程度增加
p115和MIF表达增高
提示二者可能与肿瘤细胞的异常分化有关。
Objective: To observe and compare the expressions and cellular distributions of p115 and MIF in a normal human hepatic cell line(LO2) and different hepatocellular carcinoma cell lines(SMCC-7721
HepG2).Methods: The expressions of p115 and MIF proteins were measured using Western blot analysis.The mRNA levels of p115 and MIF were detected by reverse transcription polymerase chain reaction(RT-PCR).p115 and MIF expressions were further studied with immunocytochemistry techniques.Results: The results of RT-PCR and Western blot showed that the expressions of p115 and MIF of control group(LO2) were obviously weaker than that of those HepG2 and SMCC-7721;furthermore
in HepG2 the expressions were weaker than in SMCC-7721.The results of immunohistochemical cell staining of the p115 showed that yellow or brown granules were located in the cytoplasm in different hepatocellular carcinoma cells(SMCC-7721
HepG2)
but in LO2 cells most of them were located on the Golgi complex.The cell staining for MIF was located in the cytoplasm of the normal hepatic cell line and in the different hepatocelluar carcinoma cells.Moreover
The expression of MIF in LO2 was weaker than that of HepG2
and that of HepG2 was weaker than that of SMCC-7721.Conclusion: The expressions of p115 and MIF in different hepatocellular carcinoma cells are dramatically higher than those in the normal human hepatic cell line
and p115 and MIF are strongly expressed in the SMCC-7721 cell line.The expressions and distributions of p115 and MIF are related to the stage of differentiation of cancer cells.
高尔基体转运蛋白p115巨噬细胞移动抑制因子SMCC-7721HepG2LO2
p115MIFSMCC-7721HepG2LO2
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