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[缺氧对肝星状细胞基质金属蛋白酶-2表达及活性的影响]

[Effects of hypoxia on expression and activity of matrix metalloproteinase-2 in hepatic stellate cell].

作者信息

Chen P, Zhai W, Zhang Y, Zhang J, Gu Y

机构信息

Shanghai Medical University, Shanghai 200032, China.

出版信息

Zhonghua Gan Zang Bing Za Zhi. 2000 Oct;8(5):276-8.

PMID:11058950
Abstract

OBJECTIVE

To study the effect of hypoxia on the expression and activity of matrix metalloproteinase-2 (MMP-2) in the hepatic stellate cell (HSC).

METHODS

The expression of MMP-2 and tissue inhibitor of metalloproteinase-2 (TIMP-2) in cultured rat HSC was detected by immunocytochemistry (ICC). The relative amount of MMP-2 and TIMP-2 in the culture supernatant was assayed by ELISA and the activity of MMP-2 in supernatant was examined by zymography.

RESULTS

The expression of MMP-2 was enhanced in hypoxia group as compared with that in control one (t' 3.4685, P<0.05 ), while the expression of TIMP-2 was decreased (t'=2.5673, P<0.05). The activity of MMP-2 was lower in hypoxia group than in control one (t'=4.270, P<0.01). Comparing the varied duration of hypoxia, the relative amount of MMP-2 protein was the highest in 6 h group (6h vs 12h, t=4. 0945, P<0.001; 6h vs 24h, t=2.4652, P<0.025), with a contrary curve in TIMP-2.

CONCLUSION

Hypoxia promotes the expression of MMP-2 and inhibits the expression of TIMP-2 in HSC. It is more notable at early stage of hypoxia.

摘要

目的

研究缺氧对肝星状细胞(HSC)中基质金属蛋白酶-2(MMP-2)表达及活性的影响。

方法

采用免疫细胞化学法(ICC)检测培养的大鼠HSC中MMP-2和金属蛋白酶组织抑制剂-2(TIMP-2)的表达。用酶联免疫吸附测定法(ELISA)检测培养上清液中MMP-2和TIMP-2的相对含量,并用酶谱分析法检测上清液中MMP-2的活性。

结果

与对照组相比,缺氧组MMP-2的表达增强(t' = 3.4685,P < 0.05),而TIMP-2的表达降低(t' = 2.5673,P < 0.05)。缺氧组MMP-2的活性低于对照组(t' = 4.270,P < 0.01)。比较不同缺氧时间,MMP-2蛋白相对含量在6小时组最高(6小时 vs 12小时,t = 4.0945,P < 0.001;6小时 vs 24小时,t = 2.4652,P < 0.025),TIMP-2呈相反趋势。

结论

缺氧促进HSC中MMP-2的表达并抑制TIMP-2的表达。在缺氧早期这种作用更显著。

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引用本文的文献

1
Effects of hypoxia, hyperoxia on the regulation of expression and activity of matrix metalloproteinase-2 in hepatic stellate cells.缺氧、高氧对肝星状细胞中基质金属蛋白酶-2表达及活性调控的影响
World J Gastroenterol. 2001 Oct;7(5):647-51. doi: 10.3748/wjg.v7.i5.647.