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TGF-beta s stimulate cell proliferation via an autocrine production of FGF-2 in corneal stromal fibroblasts

Authors
 EunDuck P. Kay  ;  Moon Shin Lee  ;  Gong Je Seong  ;  Young Ghee Lee 
Citation
 CURRENT EYE RESEARCH, Vol.17(3) : 286-293, 1998 
Journal Title
 CURRENT EYE RESEARCH 
ISSN
 0271-3683 
Issue Date
1998
MeSH
Animals ; Cell Count ; Cell Cycle Proteins* ; Cell Division/drug effects ; Cells, Cultured ; Corneal Stroma/cytology* ; Corneal Stroma/drug effects ; Corneal Stroma/metabolism ; Cyclin-Dependent Kinase Inhibitor p27 ; DNA Replication ; Dose-Response Relationship, Drug ; Electrophoresis, Polyacrylamide Gel ; Fibroblast Growth Factor 2/biosynthesis* ; Fibroblasts/cytology ; Fibroblasts/drug effects ; Fibroblasts/metabolism ; Immunoenzyme Techniques ; Microtubule-Associated Proteins/biosynthesis ; Oligonucleotides, Antisense/chemistry ; Rabbits ; Receptors, Transforming Growth Factor beta/biosynthesis ; Transforming Growth Factor beta/biosynthesis ; Transforming Growth Factor beta/pharmacology* ; Tumor Suppressor Proteins* ; Up-Regulation
Abstract
PURPOSE: Although transforming growth factor-betas (TGF-beta s) inhibit epithelial cell proliferation, these same substances stimulate cell proliferation of fibroblasts. In order to elucidate the mechanism of stimulatory activity of TGF-beta on fibroblast, the present study was performed to determine whether TGF-beta might be an indirect mitogen acting through induction of an endogenous growth factor(s) that then acts as the direct mitogen in an autocrine manner in corneal stromal fibroblasts (CSFs). METHODS: Cell proliferation was determined either by counting cell numbers or by analyzing the incorporation of [3H]-thymidine into DNA. The synthesis of TGF-beta, TGF-beta receptors, FGF-2 and p27 was analyzed by immunoprecipitation and immunoblotting. RESULTS: TGF-beta 1, TGF-beta 2, and TGF-beta 3 significantly stimulated cell proliferation of CSFs in a dose-dependent manner. The medium conditioned by CSFs and subsequently activated by acid-inhibited cell proliferation of corneal endothelial cells by 40%. When the acid-activated media conditioned by CSFs were immunoprecipitated with either combined anti-TGF-beta 1 and TGF-beta 2 antibodies or anti-TGF-beta 3 antibody, all three TGF-beta s, with an apparent molecular size of 25 kDa, were detected, whereas CSFs produced an 80-kDa latent form of TGF-beta 1. These cells can also express TGF-beta type II receptor and betaglycan. Interestingly, CSFs produced and secreted 18-kDa FGF-2, the synthesis of which is further stimulated by either TGF-beta 1 or TGF-beta 3, while both the neutralizing antibody to FGF-2 and the FGF-2 specific antisense oligonucleotide primers significantly inhibited the stimulatory activities of TGF-beta 1 in CSFs. The expression of p27, a negative regulator in cell cycle, was not altered by TGF-beta. CONCLUSIONS: These findings indicate that CSFs produce both TGF-beta s and FGF-2 and that FGF-2 appears to be a direct stimulator for TGF-beta-mediated cell proliferation in CSFs.
Full Text
https://www.tandfonline.com/doi/abs/10.1076/ceyr.17.3.286.5212
DOI
10.1076/ceyr.17.3.286.5212
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Ophthalmology (안과학교실) > 1. Journal Papers
Yonsei Authors
Seong, Gong Je(성공제) ORCID logo https://orcid.org/0000-0002-5456-4296
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/176740
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