Connective tissue growth factor modulates extracellular matrix production in human subconjunctival fibroblasts and their proliferation and migration in vitro
Autor: | Ai Kitano, Osamu Yamanaka, Ken-ichi Miyazaki, Yoshitaka Ohnishi, Shizuya Saika, Kazuo Ikeda |
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Rok vydání: | 2008 |
Předmět: |
medicine.medical_treatment
Enzyme-Linked Immunosorbent Assay Collagen Type I DNA Antisense Immediate-Early Proteins Transforming Growth Factor beta1 Extracellular matrix Cell Movement medicine Humans RNA Messenger Child Cells Cultured Cell Proliferation integumentary system biology Reverse Transcriptase Polymerase Chain Reaction Chemistry Growth factor Connective Tissue Growth Factor General Medicine Fibroblasts Oligonucleotides Antisense Extracellular Matrix Fibronectins Cell biology Collagen Type I alpha 1 Chain Fibronectin CTGF Ophthalmology Transforming growth factor beta 3 Child Preschool Immunology biology.protein Intercellular Signaling Peptides and Proteins Wound healing Conjunctiva Type I collagen Transforming growth factor |
Zdroj: | Japanese Journal of Ophthalmology. 52:8-15 |
ISSN: | 1613-2246 0021-5155 |
DOI: | 10.1007/s10384-007-0497-3 |
Popis: | We examined the role of connective tissue growth factor (CTGF) in transforming growth factor beta1 (TGFbeta1)-related behavior in cultured human subconjunctival fibroblasts (SCFs), protein production, mRNA expression of CTGF and type I collagen alpha1 chain (colIA1), and cell proliferation and migration. TGFbeta1 is the major factor involved in bleb scarring following filtration surgery.An antisense deoxynucleotide (antisense) (5 microM) for CTGF mRNA was used to block endogenous CTGF expression. Effects of antisense on extracellular matrix (ECM) production and immunolocalization, mRNA expression, and cell proliferation and migration were examined in human SCF cultures with or without TGFbeta1 (5 ng/ml). Cell migration was examined in an in vitro wound model of monolayer fibroblast cultures.CTGF antisense reduced mRNA expression of CTGF and colIA1 and production of the ECM components type I collagen, and fibronectin much more markedly in cells treated with TGFbeta1 compared with control fibroblasts, and it inhibited the proliferation of cultured SCFs to 71.9% of that of controls after 13 days of culture. CTGF antisense also delayed defect closure in monolayer cell sheets. In the culture, the defect was closed by TGFbeta1 by 36 h, whereas 7.0% of the defect remained at 48 h in the antisense-treated culture.These findings indicate that CTGF is involved in ECM production in SCFs activated by exogenous TGFbeta1 in vitro. Inhibition of CTGF expression may be effective in preventing undesirable scar formation during healing following filtration surgery. |
Databáze: | OpenAIRE |
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