Indirect mitogenic effect of transforming growth factor-β on cell proliferation of subconjunctival fibroblasts

Investigative Ophthalmology and Visual Science

Volumn 39, Issue 3, 1998, Pages 481-486

  Kay, EunDuck P ^a,b,c   Lee, Hyung Keun ^a   Park, Kee Soon ^a   Lee, Sung Chul ^a  

^a Yonsei University College of Medicine   (South Korea)

^b UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^c DOHENY EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR 2; TRANSFORMING GROWTH FACTOR ALPHA; TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA3;

ARTICLE; CELL COUNT; CELL PROLIFERATION; CONJUNCTIVA; CORNEA STROMA; FIBROBLAST; FIBROSIS; FILTERING OPERATION; GLAUCOMA; HUMAN; HUMAN CELL; IMMUNOBLOTTING; IMMUNOPRECIPITATION; MITOGENESIS; PRIORITY JOURNAL;

ANIMALS; CELL COUNT; CELL DIVISION; CELLS, CULTURED; CONJUNCTIVA; CULTURE MEDIA, CONDITIONED; DNA; DNA REPLICATION; DOSE-RESPONSE RELATIONSHIP, DRUG; FIBROBLAST GROWTH FACTOR 2; FIBROBLASTS; IMMUNOBLOTTING; MITOGENS; OLIGONUCLEOTIDES, ANTISENSE; PRECIPITIN TESTS; RABBITS; TRANSFORMING GROWTH FACTOR BETA;

EID: 2642645425     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (27)

1. Massague J. The transforming growth factor-β family. Annu Rev Cell Biol. 1990;6:597-641.
2. Wrana JL, Attisano L, Wieser R., et al. Mechanism of activation of the TGF-β receptor. Nature. 1994;370:341-347.
3. Sporn MB, Roberts AB. Transforming growth factor β: recent progress and new challenges. J Cell Biol. 1992;119:1017-1021.
4. Ewen ME, Sluss HK, Sherr CJ, Matsushine H, Kato J, Livingston DM. TGF-β inhibition of Cdk4 synthesis is linked to cell cycle arrest. Cell. 1993;74:1009-1020.
5. Koff A, Ohtsuki M, Polyak K, Roberts JM, Massague J. Negative regulation of G1 in mammalian cells: inhibition of cyclin E-dependent kinase by TGF-β. Science. 1993;260:536-539.
6. Polyak K, Kato JY, Solomon MJ, Sherr CJ, Massague J, Roberts JM, Koff A. p27kip1, a cyclin-cdk inhibitor, links transforming growth factor-β and contact inhibition to cell cycle arrest. Genes Dev. 1994;8:9-22.
7. Jones SC, Curtsinger LJ, Whalen JD, et al. Effect of topical recombinant TGF-β on healing of partial thickness injuries. J Surg Res. 1991;51:344-352.
8. Soma Y, Grotendorst FR. TGF-β stimulates primary human skin fibroblast DNA synthesis via an autocrine production of PDGF-related peptides. J Cell Physiol. 1989;140:246-253.
9. Majack RA, Majesky MW, Goodman LV. Role of PDGF-A expression in the control of vascular smooth muscle cell growth by transforming growth factor-β. J Cell Biol. 1990;111:239-247.
10. Kimelman D, Kirschner M. Synergistic induction of mesoderm by FGF and TGF-β and the identification of an mRNA coding for FGF in early Xenopus embryo. Cell. 1987;51:869-877.
11. Plouet J, Gospodarowicz D. Transforming growth factor β-1 positively modulates the bioactivity of fibroblast growth factor on corneal endothelial cells. J Cell Physiol. 1989;141:392-399.
12. Jampel HD. Ascorbic acid is cytotoxic to dividing human Tenon's capsule fibroblasts. Arch Ophthalmol. 1990;108:1323-1325.
13. Bradford MM. Rapid and sensitive method for the quantitiation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248-253.
14. Gu X, Seong GJ, Lee YG, Kay EP. Fibroblast growth factor 2 uses distinct signaling pathways for cell proliferation and cell shape changes in corneal endothelial cells. Invest Ophthalmol Vis Sci. 1996;37:2326-2334.
15. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227:680-685.
16. 3H]adenine metabolism and radiation damage during in vitro development of the kidney. J Histochem Cytochem. 1992;40:1173-1182.
17. Gentry LE, Nash BW. The pro domain of pre-pro-transforming growth factor β1 when independently expressed is a functional binding protein for the mature growth factor. Biochemistry. 1990; 29:6851-6857.
18. Lyons RM, Keski-Oja J, Moses HL. Proteolytic activation of latent transforming growth factor-β from fibroblast-conditioned medium. J Cell Biol. 1988;106:1659-1665.
19. Olofsson A, Miyazono K, Kanzaki T, Colosetti P, Engstrom U, Heldins C-H. Transforming growth factor-β1, -β2, and β3 secreted by a human glioblastoma cell line. Identification of small and different forms of large latent complexes. J Biol Chem. 1992;267: 19482-19488.
20. Lioubin MN, Madisen L, Marquardt H, Roth R, Kovacina KS, Purchio AF. Characterization of latent recombinant TGF-β2 produced by Chinese hamster ovary cells. J Cell Biochem. 1991;45:112-121.
21. Starksen NF, Harsh GR 4th, Gibbs VC, Williams LT. Regulated expression of the platelet-derived growth factor A chain gene in microvascular endothelial cells. J Biol Chem. 1987;262:14381-14384.
22. Leof EB, Proper JA, Goustin AS, Shipley GD, DiCorleto PE, Moses HL. Induction of c-sis mRNA and activity similar to platelet-derived growth factor by transforming growth factor β: a proposed model for indirect mitogenesis involving autocrine activity. Proc Natl Acad Sci USA. 1986;83:2453-2457.
23. Mason IJ. The ins and outs of fibroblast growth factors. Cell. 1994;78:547-552.
24. Attisano L, Wrana JL, Lopez-Casillas F, Massague J. TGF-β receptors and actions. Biochim Biophys Acta. 1994;1222:71-80.
25. Sato Y, Okada F, Abe M, et al. The mechanism for the activation of latent TGF-β during co-culture of endothelial cells and smooth muscle cells: cell-type specific targeting of latent TGF-β to smooth muscle cells. J Cell Biol. 1993;123:1249-1254.
26. Purchio AF, Cooper JA, Brunner AM, et al. Identification of mannose-6-phosphate in two asparagine-linked sugar chains of recombinant transforming growth factor-β1 precursor. J Biol Chem. 1988;263:14211-14215.
27. Jirtle RL, Haag JD, Ariazi EA, Gould MN. Increased mannose-6-phosphate/insulin-like growth factor II receptor and transforming growth factor β1 levels during monoterpene-induced regression of mammary tumors. Cancer Res. 1993;53:3849-3852.