Role of connective growth factor in plasminogen activator inhibitor-1 and fibronectin expression induced by transforming growth factor beta1 in renal tubular cells.
- Author:
Chun ZHANG
1
;
Xian-fang MENG
;
Zhong-hua ZHU
;
Xiao YANG
;
An-guo DENG
Author Information
- Publication Type:Journal Article
- MeSH: Cells, Cultured; Connective Tissue Growth Factor; Extracellular Matrix; metabolism; Fibronectins; genetics; secretion; Humans; Immediate-Early Proteins; genetics; physiology; Intercellular Signaling Peptides and Proteins; genetics; physiology; Kidney Tubules; metabolism; Oligonucleotides, Antisense; pharmacology; Plasminogen Activator Inhibitor 1; genetics; secretion; RNA, Messenger; analysis; Transfection; Transforming Growth Factor beta; pharmacology; Transforming Growth Factor beta1
- From: Chinese Medical Journal 2004;117(7):990-996
- CountryChina
- Language:English
-
Abstract:
BACKGROUNDConnective tissue growth factor (CTGF) contributes greatly to renal tubulointerstitial fibrosis, which is the final event leading to end-stage renal failure. This study was designed to investigate the effects of CTGF antisense oligodeoxynucleotides (ODNs) on the expressions of plasminogen activator inhibitor-1 (PAI-1) and fibronectin in renal tubular cells induced by transforming growth factor beta1 (TGF-beta1) in addition to the role of CTGF in the accumulation and degradation of renal extracellular matrix (ECM).
METHODSA human proximal tubular epithelial cell line (HKC) was cultured in vitro. Cationic lipid-mediated CTGF antisense ODNs were transfected into HKC cells. After HKC cells were stimulated with TGF-beta1 (5 microg/L), the mRNA levels of PAI-1 and fibronectin were measured by RT-PCR. Intracellular PAI-1 protein synthesis was assessed by flow cytometry. The secreted PAI-1 and fibronectin in the medium were determined by Western blot and ELISA, respectively.
RESULTSTGF-beta1 was found to induce tubular CTGF, PAI-1, and fibronectin mRNA expression. PAI-1 and fibronectin mRNA expression induced by TGF-beta1 was significantly inhibited by CTGF antisense ODNs. CTGF antisense ODNs also inhibited intracellular PAI-1 protein synthesis and lowered the levels of PAI-1 and fibronectin protein secreted into the medium.
CONCLUSIONSCTGF may play a crucial role in the accumulation and degradation of excessive ECM during tubulointerstitial fibrosis, and transfecting CTGF antisense ODNs may be an effective way to prevent renal fibrosis.