Influence of Hepatocyte Growth Factor on Matrix Metalloproteinase Expression in HT cell line.
- Author:
Jong Chul SHIN
1
;
Hee Bong MOON
;
Jee Hyun LEE
;
Dong Eun YANG
;
Guisera LEE
;
Young LEE
;
Jong Seong LEE
;
Chang Yi KIM
;
Soo Pyung KIM
Author Information
1. Department of Obstetrics and Gynecology, Medical College, Catholic University, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Trophoblast;
hepatocyte growth factor;
matrix metalloproteinase-2;
matrix metalloproteinase-9
- MeSH:
Blotting, Western;
Cell Line*;
Hepatocyte Growth Factor*;
Hepatocytes*;
Matrix Metalloproteinase 2;
Matrix Metalloproteinase 9;
Matrix Metalloproteinases;
RNA;
RNA, Messenger;
Trophoblasts
- From:Korean Journal of Obstetrics and Gynecology
2001;44(12):2257-2262
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: This study was performed to investigate the influence of hepatocyte growth factor (HGF) on matrix metalloproteinase (MMP), which are related in the lysis process of tissue during the invasion of trophoblasts. METHOD: HT cell line was treated with recombinant HGF (rHGF) of different concentration (0, 10, 50 and 100 ng/mL) and was cultured for 24 hours to check the changes in the expression of MMP-2 and MMP-9. Also, HT cell line was treated with recombinant HGF 50 ng/mL and was cultured for 24, 36, 48, and 72 hours to check the changes in the expression of MMPs according to the different time span. Total RNA were extracted from each cultured sample and RT-PCR and Western blotting were used to analyze the expression of MMP-2 and MMP-9. RESULTS: MMP-2 mRNA expression with treated rHGF showed increase of 2, 2.5 and 2.2 times with the increase of concentration level of 10, 50 and 100 ng/mL accordingly, while MMP-2 protein expression were increased 1.4 and 1.5 times in 50 ng/mL and 100 ng/mL of rHGF respectively compared with that of normal control. MMP-9 mRNA showed no significant changes in its expression with all different levels of concentration, while MMP-9 protein showed 1.5 times increase with 10 ng/mL rHGF but 0.4 times decrease with 100 ng/mL. MMP-2 mRNA expression treated with recombinat HGF were increased 1.6 times with 24 hour culture and 2.3 times with 36 hour culture. MMP-2 protein showed 1.9 times increase only for the case of 24 hour culture. MMP-9 mRNA expression of recombinant HGF-treated groups was decreased 0.7 times compared with that of control group in 36 hours. MMP-9 protein expression were increased by 1.2, 1.6 and 1.9 times as culture time increase to 36, 48, and 72 hours accordingly, compared with that of normal control. CONCLUSION: This result suggests that the HGF might partially regulate the invasion of trophoblasts through MMP-2 and MMP-9.
