TGF-ß elicits fibronectin secretion and proliferation in cultured chick lens epithelial cells

References

• Sporn, M. B., Roberts, A. B. (1992) Transforming growth factor-f3: recent progress and new challenges. J Cell Biol 119, 1017–1021.
   PubMed Web of Science ®Google Scholar
• Liu, J., Hales, A. M., Chamberlain, C. G., McAvoy, J. W. (1994) Induction of cataract-like changes in rat lens epithelial explants by transforming growth factor-I3. In-vest Ophthalmol Vis Sci 35, 388–401.
   PubMed Web of Science ®Google Scholar
• Hales, A. M., Chamberlain, C. G., McAvoy, J. W. (1995) Cataract induction in lenses cultured with transforming growth factor-I3. Invest Ophthalmol Vis Sci 36, 1709–1713.
   PubMed Web of Science ®Google Scholar
• Jampel, H. D., Roche, N., Stark, W. J., Roberts, A. B. (1990) TGF-f3 in human aqueous humor. Curr Eye Res 9, 963–969.
   PubMed Web of Science ®Google Scholar
• Cousins, S. W., McCabe, M. M., Danielpour, D., Streilein, J. W. (1990) Identification of transforming growth fac-tor-beta as an immunosuppressive factor in aqueous hu-mor. Invest Ophthalmol Vis Sci 32, 2201–2211.
   Google Scholar
• Lutty, G. A., Merges, C., Threlkeld, A. B., Crone, S., McLeod, D.S. (1993) Heterogeneity in localization of isoforms of TGF-f3 in human retina, vitreous and chor-oid. Invest Ophthalmol Vis Sci 34, 477–487.
   PubMed Web of Science ®Google Scholar
• Pe1ton, R. W., Saxena, B., Jones, M., Moses, H. L., Gold, L. I. (1991) Immunohistochemical localization of TGF-f31, TGF-f32 and TGF-f33 in mouse embryo: expression patterns suggest multiple roles during embryonic devel-opment. J Cell Biol 115, 1091–1105.
   Google Scholar
• Potts, J.D., Bassnett, S., Beebe, D. C. (1995) Expression of transforming growth factor f3 in embryonic avian lens coincides with the presence of mitochondria. Develop-mental Dynamics 203, 317–323.
   PubMedGoogle Scholar
• Derynck, R. (1994) TGF-f3-receptor-mediated signaling. TIBS 19, 548–553.
   PubMed Web of Science ®Google Scholar
• Massagué, J. (1992) Receptors for the TGF-f3 family. Cell 69, 1067–1070.
   PubMed Web of Science ®Google Scholar
• Hatae, T., Ishibashi, T., Yoshitomi, F., Shibata, Y. (1993) Immunocytochemistry of types I-IV collagen in human anterior subcapsular cataracts. Graefe's Arch Clin Exp Ophthalmol 231, 586–590.
   PubMed Web of Science ®Google Scholar
• Nishi, 0., Nishi, K., Fujiwara, T., Shirasawa, E. (1995) Types of collagen synthesized by the lens epithelial cells of human cataracts. Br J Ophthalmol 79, 939–943.
   Google Scholar
• Nishi, 0., Nishi, K., Fujiwara, T., Shirasawa, E., Ohmoto, Y. (1996) Effects of the cytokines on the proliferation of and collagen synthesis by human cataract lens epi-thelial cells. Br J Ophthalmol 80, 63–68.
   Google Scholar
• Hales, A. M., Schulz, M. W., Chamberlain, C. G., McAvoy, J. W. (1994) TGF-I31 induces lens cells to ac-cumulate a-smooth muscle actin, a marker for subcap-sular cataracts. Curr Eye Res 13, 885–890.
   PubMed Web of Science ®Google Scholar
• Kurosaka, D., Kato, K., Nagamoto, T., Negishi, K. (1995) Growth factors influence contractility and a-smooth muscle actin expression in bovine lens epithelial cells. Invest Ophthalmol Vis Sci 36, 1701–1708.
   PubMed Web of Science ®Google Scholar
• Kurosaka, D., Nagamoto, T. (1994) Inhibitory effect of TGF-f32 in human aqueous humor on bovine lens epi-thelial cell proliferation. Invest Ophthalmol Vis Res 35, 3408–3412.
   PubMedGoogle Scholar
• Srinivasan, Y., Lovicu, F. J., Overbeek, P. A. (1998) Lens-specific expression of transforming growth factor f31 in transgenic mice causes anterior subcapsular cataracts. J Clin Invest 101, 625–634.
   PubMed Web of Science ®Google Scholar
• Ireland, M. E., Tran, K., Mrock, L. (1993) f3-adrenergic mechanisms affect cell division and differentiation in cul-tured chick lens epithelial cells. Exp Eye Res 57, 325–333.
   PubMedGoogle Scholar
• Ireland, M. E., Braunsteiner, A., Mrock, L. (1993) Cell-cell interactions affect the accumulation of a cytokeratin-like protein during lens fiber development. Developmental Riol 160, 494–503.
   Google Scholar
• Fridman, R., Fuks, Z., Ovadia, H., Vlodavsky, I. (1985) Differential structure requirements for the induction of cell attachment, proliferation and differentiation by ex-tracellular matrix. Exp Cell Res 157, 181–194.
   PubMedGoogle Scholar
• Laemmli, U. K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680–685.
   PubMed Web of Science ®Google Scholar
• Ireland, M. E., Jacks, L. A. (1989) Initial characteriza-tion of lens beta-adrenergic receptors. Invest Ophthalmol Vis Res 30, 2190–2194.
   PubMed Web of Science ®Google Scholar
• Henkel, A. W., Bieger, S. C. (1994) Quantification of proteins dissolved in an electrophoresis sample buffer. Anal Biochem 223, 329–331.
   PubMed Web of Science ®Google Scholar
• Tripathi, R. C., Li, J., Chan, W. F. A., Tripathi, B. J. (1994) Aqueous humor in glaucomatous eyes contains an increased level of TGF-I32. Exp Eye Res 59, 723–728.
   PubMed Web of Science ®Google Scholar
• Le, D., Gordon, L. W., Glaser, B. M., Pena, R. A. (1994) Transforming growth factor-beta 2 levels increase fol-lowing retinal laser photocoagulation. Curr Eye Res 13, 743–746.
   PubMedGoogle Scholar
• Wrana, J.L., Attisano L., Wieser, R., Ventura, F., Massagué, J. (1994) Mechanisms of activation of the TGF-f3 receptor. Nature 370, 341–347.
   PubMed Web of Science ®Google Scholar
• Piatigorsky, J. (1981) Lens differentiation in vertebrates: a review of cellular and molecular features. Differentia-tion 19, 134–153.
   PubMed Web of Science ®Google Scholar
• Obata, H., Kaburaki, T., Kato, M., Yamashita, H. (1996) Expression of TGF-f3 type I and type II receptors in rat eyes. Curr Eye Res 15, 335–340.
   PubMed Web of Science ®Google Scholar
• Hyatt, G. A., Beebe, D. C. (1993) Regulation of lens cell growth and polarity by an embryo-specific growth fac-tor and by inhibitors of lens cell proliferation and dif-ferentiation. Development 117, 701–709.
   PubMed Web of Science ®Google Scholar
• Potts, J. D., Harocopos, G. J., Beebe, D. C. (1993) Iden-tification of receptor tyrosine kinases in the embryonic chicken lens. Curr Eye Res 12, 759–763.
   PubMed Web of Science ®Google Scholar
• Cammarata, P. R., Spiro, R. G. (1985) Identification of noncollagenous components of calf lens capsule: evalu-ation of their adhesion-promoting activity. J Cell Physiol 125, 393–402.
   PubMed Web of Science ®Google Scholar
• Parmigiani, C. M., McAvoy, J. W. (1991) The roles of laminin and fibronectin in the development of the lens capsule. Curr Eye Res 10, 501–511.
   PubMed Web of Science ®Google Scholar
• Olivero, D. K., Furcht, L. T. (1993) Type IV collagen, laminin and fibronectin promote the adhesion and mi-gration of rabbit lens epithelial cells in vitro. Invest Ophthalmol Vis Res 34, 2825–2834.
   PubMed Web of Science ®Google Scholar
• Tassin, J., Jacquemin, E., Courtois, Y. (1983) Interac-tion of bovine epithelial lens (BEL) cells with extracel-lular matrix (ECM) and eye-derived growth factor (EDGF). I. Effects on short-term adhesiveness and on long-term organization of the culture. Exp Cell Res 149, 69–84.
   Google Scholar
• Iwig, M., Glaesser, D., Bethge, M. (1981) Cell shape-mediated growth control of lens epithelial cells grown in culture. Exp Cell Res 131, 47–55.
   PubMedGoogle Scholar
• Muggleton-Harris, A. L., Higbee, N. (1987) Factors modu-lating mouse lens epithelial cell morphology with dif-ferentiation and development of a lentoid structure in vitro. Development 99, 25–32.
   Google Scholar
• Nishi, 0., Nishi, K., Akaishi, T., Shirasawa, E. (1997) Detection of cell adhesion molecules in lens epithelial cells of human cataracts. Invest Ophthalmol Vis Sci 38, 579–585.
   Google Scholar
• Kern, P., Laurent, M., Lim, A., Regnault, F., Courtois, Y. (1983) Interaction of bovine epithelial lens (BEL) cells with extracellular matrix (ECM) and eye-derived growth factor (EDGF). II. Partial re-expression of differentiated collagen distribution and phenotype. Exp Cell Res 149, 85–93.
   PubMedGoogle Scholar
• Lovicu, F. J., Chamberlain, C. G., McAvoy, J. W. (1995) Differential effects of aqueous and vitreous on fiber dif-ferentiation and extracellular matrix accumulation in lens epithelial explants. Invest Ophthalmol Vis Sci 36, 1459–1469.
   PubMed Web of Science ®Google Scholar
• Courtois, Y., Arruti, C., Barritault, D., Tassin, J., Olivie, M., Hughes, R. C. (1981) Modulation of the shape of epithelial lens cells in vitro directed by a retinal extract factor. Differentiation 18, 11–27.
   PubMed Web of Science ®Google Scholar
• Kennedy, A., Frank, R. N., Sotolongo, L. B., Das A., Zhang, N. L. (1990) Proliferative response and macro-molecular synthesis by ocular cells cultured on extra-cellular matrix materials. Curr Eye Res 9, 307–322.
   Google Scholar
• Arita, T., Murata, Y., Lin, L. R., Tsuji, T., Reddy, V. N. (1993) Synthesis of lens capsule in long-term culture of human lens epithelial cells. Invest Ophthalmol Vis Sci 34, 355–362.
   PubMedGoogle Scholar
• Delcommenne, M., Streuli, C. H. (1995) Control of integrin expression by extracellular matrix. J Riol Chem 270, 26794–26801.
   Google Scholar
• Fitch, J. M., Mayne, R., Linsenmayer, T. F. (1983) De-velopmental acquisition of basement membrane hetero-geneity: type IV collagen in avian lens capsule. J Cell Riol 97, 940–943.
   Google Scholar
• Cammarata, P. R., Spiro, R. G. (1985) Identification of noncollagenous components of calf lens capsule: evalu-ation of their adhesion-promoting activity. J Cell Physiol 125, 393–402.
   PubMed Web of Science ®Google Scholar
• Laurent, M., Romquin, N., Courtois, M. F., Muel. A. S., Courtois, Y. (1987) Collagen synthesis by long-lived mRNA in embryonic chicken lens. Developmental Riol 121, 166–173.
   Google Scholar
• Haddad, A., Bennett, G. (1988) Synthesis of lens cap-sule and plasma membrane glycoproteins by lens epi-thelial cells and fibers in the rat. Amer J Anat 183, 212–225.
   PubMedGoogle Scholar
• Johnson, M. C., Beebe, D. C. (1984) Growth, synthesis and regional specialization of the embryonic chicken lens capsule. Exp Eye Res 38, 579–592.
   PubMed Web of Science ®Google Scholar
• Mohan, P. S., Spiro, R. G. (1986) Macromolecular or-ganization of basement membranes. J Riol Chem 261, 4328–4336.
   Google Scholar
• Webster, E.H., SearIs, R. L., Hilfer, S. R., Zwaan, J. (1987) Accumulation and distribution of sulfated mate-rials in the maturing mouse lens capsule. Anat Record 218, 329–337.
   PubMedGoogle Scholar
• Zwaan, J., Williams., R. M. (1969) Cataracts and abnor-mal proliferation of the lens epithelium in mice carry-ing the CatFr gene. Exp Eye Res 8, 161–167.
   Google Scholar
• Haloui, Z., Jeanny, J. C., Jonet, L., Courtois, Y., Laurent, M. (1988) Immunochemical analysis of extracellular ma-trix during embryonic lens development of the Cat Fraser mouse. Exp Eye Res 46, 463–474.
   PubMed Web of Science ®Google Scholar
• Haloui, Z., Pujol, J. P., Galera, P., Courtois, Y., Laurent, M. (1990) Analysis of lens protein synthesis in a cata-ractous mutant mouse: the Cat Fraser. Exp Eye Res 51, 487–494.
   PubMedGoogle Scholar
• Gonzalez-Avila, G., Lozano, D., Manjarrez, M. E., Ruiz, V. M., Teran, L., Vadillo-Ortega, F., Selman, M. (1995) Influence on collagen metabolism of vitreous from eyes with proliferative vitreoretinopathy. Ophthalmology 102, 1400–1405.
   Google Scholar
• Schultz-Cherry, S., Chen, H., Mosher, D. F., Misenheimer, T. M., Krutzsch, H. C., Roberts, D. D., Murphy-Ullrich, J. E. (1995) Regulation of TGF-J3 activation by discrete sequences of thrombospondin 1. JBiol Chem 270, 7304–7310.
   PubMed Web of Science ®Google Scholar