Original Research
Copyright ©The Author(s) 2001. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 15, 2001; 7(5): 647-651
Published online Oct 15, 2001. doi: 10.3748/wjg.v7.i5.647
Effects of hypoxia, hyperoxia on the regulation of expression and activity of matrix metalloproteinase-2 in hepatic stellate cells
Ping-Sheng Chen, Wei-Rong Zhai, Xiao-Mei Zhou, Jin-Sheng Zhang, Yue-E Zhang, Yu-Qin Ling, Ying-Hong Gu
Ping-Sheng Chen, Wei-Rong Zhai, Jin-Sheng Zhang, Yue-E Zhang, Yu-Qin Ling, Ying-Hong Gu, Department of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China
Ping-Sheng Chen, Department of Pathology, School of Basic Medical Sciences the (former Nanjing Railway Medical College), Southeast University, Nanjing 210009, China
Xiao-Mei Zhou, Institute of Cancer Research, Shanghai 200032, China
Author contributions: All authors contributed equally to the work.
Supported by the Scientific Research Fund for Doctorate Education, State Educational Commission, No.9837
Correspondence to: Dr. Wei-Rong Zhai, Department of Pathology, School of Basic Medical Sciences, Fudan University, 138 Yixueyuan Road, Shanghai 200032, China. wrzhai@online.sh.cn
Telephone: +86-21-64041900 Ext.2536 (O)
Received: March 19, 2001
Revised: June 6, 2001
Accepted: June 12, 2001
Published online: October 15, 2001
Abstract

AIM: To study the effects of hypoxia, hyperoxia on the regulation of expression and activity of matrix metalloproteinase-2 (MMP-2) in hepatic stellate cells (HSC).

METHODS: The expressions of MMP-2, tissue inhibitor of matrix metalloproteinase-2 (TIMP-2) and membrane type matrix metalloproteinase-1 (MT1-MMP) in cultured rat HSC were detected by immunocytochemistry (ICC) and in situ hybridization (ISH). The contents of MMP-2 and TIMP-2 in culture supernatant were detected with ELISA and the activity of MMP-2 in supernatant was revealed by zymography.

RESULTS: In the situation of hypoxia for 12 h, the expression of MMP-2 protein was enhanced (hypoxia group positive indexes: 5.7 ± 2.0, n = 10; control: 3.2 ± 1.0, n = 7; P ＜ 0.05), while TIMP-2 protein was decreased in HSC (hypoxia group positive indexes: 2.5 ± 0.7, n = 10; control: 3.6 ± 1.0, n = 7; P ＜ 0.05), and the activity (total A) of MMP-2 in supernatant declined obviously (hypoxia group: 7.334 ± 1.922, n = 9; control: 17.277 ± 7.424, n = 11; P ＜ 0.01). Compared the varied duration of hypoxia, the changes of expressions including mRNA and protein level as well as activity of MMP-2 were most notable in 6 h group. The highest value (A hypoxia-A control) of the protein and the most intense signal of mRNA were in the period of hypoxia for 6 h, along with the lowest activity of MMP-2. In the situation of hyperoxia for 12 h, the contents (A450) of MMP-2 and TIMP-2 in supernatant were both higher than those in the control, especially the TIMP-2 (hyperoxia group: 0.0499 ± 0.0144, n = 16; control: 0.0219 ± 0.0098, n = 14; P ＜ 0.01), and so was the activity of MMP-2 (hyperoxia group: 5.252 ± 0.771, n = 14; control: 4.304 ± 1.083, n = 12; P ＜ 0.05), and the expression of MT1-MMP was increased.

CONCLUSION: HSC is sensitive to the oxygen, hypoxia enhances the expression of MMP-2 and the effect is more marked at the early stage; hyperoxia mainly raises the activity of MMP-2.

Keywords: liver/pathology; liver/metabolism; metalloproteinases/biosynthesis; metalloproteinases/metabolism; anoxia/metabolism; oxygen/pharmacology