
pmid: 17393107
In order to investigate the effects of connective tissue growth factor (CTGF) antisense oligodeoxynucleotide (ODN) on plasminogen activator inhibitor-1 (PAI-1) expression in renal tubular cells induced by transforming growth factor beta1 (TGF-beta1) and to explore the role of CTGF in the degradation of renal extracellular matrix (ECM), a human proximal tubular epithelial cell line (HKC) was cultured in vitro. Cationic lipid-mediated CTGF antisense ODN was transfected into HKC. After HKC were stimulated with TGF-beta1 (5 microg/L), the mRNA level of PAI-1 was detected by RT-PCR. Intracellular PAI-1 protein synthesis was assessed by flow cytometry. The secreted PAI-1 in the media was determined by Western blot. The results showed that TGF-beta1 could induce tubular CTGF and PAI-1 mRNA expression. The PAI-1 mRNA expression induced by TGF-beta1 was significantly inhibited by CTGF antisense ODN. CTGF antisense ODN also inhibited intracellular PAI-1 protein synthesis and lowered the levels of PAI-1 protein secreted into the media. It was concluded that CTGF might play a crucial role in the degradation of excessive ECM during tubulointerstitial fibrosis, and blocking the biological effect of CTGF may be a novel way in preventing renal fibrosis.
Time Factors, Reverse Transcriptase Polymerase Chain Reaction, Connective Tissue Growth Factor, Epithelial Cells, Oligonucleotides, Antisense, Transfection, Cell Line, Extracellular Matrix, Immediate-Early Proteins, Transforming Growth Factor beta1, Kidney Tubules, Transforming Growth Factor beta, Plasminogen Activator Inhibitor 1, Humans, Intercellular Signaling Peptides and Proteins, RNA, Messenger
Time Factors, Reverse Transcriptase Polymerase Chain Reaction, Connective Tissue Growth Factor, Epithelial Cells, Oligonucleotides, Antisense, Transfection, Cell Line, Extracellular Matrix, Immediate-Early Proteins, Transforming Growth Factor beta1, Kidney Tubules, Transforming Growth Factor beta, Plasminogen Activator Inhibitor 1, Humans, Intercellular Signaling Peptides and Proteins, RNA, Messenger
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