Tethered epidermal growth factor as a paradigm for growth factor–induced stimulation from the solid phase (original) (raw)

References

  1. Pierce, G.F. & Mustoe, T.A. Pharmacologic enhancement of wound healing. Annu. Rev. Med. 46, 467–481 (1995).
    Article CAS Google Scholar
  2. Meyer-Ingold, W. Wound therapy: Growth factors as agents to promote healing. Trends Biotech. 11, 387–392 (1993).
    Article CAS Google Scholar
  3. Lawrence, W.T. & Diegelmann, R.F. Growth factors in wound healing. Clin. Dermatol 12, 157–169 (1994).
    Article CAS Google Scholar
  4. Marshall, C.J. Specificity of receptor tyrosine kinase signaling: Transient versus sustained extracellular signal-related kinase activation. Cell 80, 179–185 (1995).
    Article CAS Google Scholar
  5. Smith, K.A. Interleukin 2: A 10-year perspective, in Interleukin 2 (ed. Smith, K.A.) 1–35 (Academic Press, San Diego, 1988).
    Google Scholar
  6. Matsumoto, K., Hashimoto, K. Makoto, H., Yoshimasa, H. & Yoshikawa, K. Modulation of growth and differentiation in normal human keratinocytes by transforming growth factor-p. J. Cell. Physiol., 145, 95–101 (1990).
    Article CAS Google Scholar
  7. Aharonov, A., Pruss, R.M. & Herschman, H.R. Epidermal growth factor: Relationship between receptor regulation and mitogenesis in 3T3 cells. J. Biol. Chem. 253, 3970–3977 (1978).
    CAS PubMed Google Scholar
  8. Schaudies, R.P., Harper, R.A. & Savage, C.R. 125I-EGF binding to responsive and nonresponsive cells in culture: Loss of cell-associated radioactivity relates to growth induction J. Cell. Physiol 124, 493–498 (1985).
    Article CAS Google Scholar
  9. Knauer, D.J., Wiley, H.S. & Cunningham, D.D. Relationship between epidermal growth factor receptor occupancy and mitogenic response: Quantitative analysis using a steady-state model system. J.Biol. Chem. 269, 5623–5631 (1984).
    Google Scholar
  10. Reddy, C.C., Wells, A. & Lauffenburger, D.A. Proliferative response of fibrob-lasts expressing internalization-deficient epidermal growth factor (EGF) receptors is altered via differential EGF depletion effect. Biotechnology Progress 10, 377–384 (1994).
    Article CAS Google Scholar
  11. Langer, R. & Vacanti, J.P. Tissue engineering. Science 260, 920–926 (1993).
    Article CAS Google Scholar
  12. Marti, U., Burwen, S.J. & Jones, A.L. Biological effects of epidermal growth factor, with an emphasis on the gastrointestinal tract and liver: An update. Hepatology 9, 126–138 (1989).
    Article CAS Google Scholar
  13. Allgor, S.S. Linear and star-shaped poly(ethylene oxide) grafted surfaces: Grafting density and protein adsorption, thesis, Massachusetts Institute of Technology (1996).
    Google Scholar
  14. Blanc, P. et al Mitotic responsiveness of cultured adult human hepatocytes to epidermal growth factor, transforming growth factor a, and human serum. Gastroenterology 102, 1340–1350 (1992).
    Article CAS Google Scholar
  15. Tomomura, A., Sawada, N., Sattler, G.L., Kleinman, H.K. & Pitot, H.C. The control of DNA synthesis in primary cultures of hepatocytes from adult and young rats: Interactions of extracellular matrix components, epidermal growth factor, and the cell cycle. J. Cell. Physiol. 130, 221–227 (1987).
    Article CAS Google Scholar
  16. Diaknova, M. et al. Epidermal growth factor induced rapid and transient association of phospolipase C-yl with EGF receptor and filamentous actin at membrane ruffles of A431 cells. J. Cell Sci. 108, 2499–2509 (1995).
    Google Scholar
  17. Welsh, J.B., Gill, G.N., Rosenfeld, M.G. & Wells, A. A negative feedback loop attenuates EGF-induced morphological changes. J. Cell Biol. 114, 533–543 (1991).
    Article CAS Google Scholar
  18. Chen, P., Gupta, K. & Wells, A. Cell movement elicited by epidermal growth factor receptor requires kinase and autophosphorylation but is separable from mitogenesis. J.Cell Biol. 124, 547–555 (1994).
    Article CAS Google Scholar
  19. Stolz, D.B. & Michalopoulos, G.K. Comparative effects of hepatocyte growth factor and epidermal growth factor on motility, morphology, mitogenesis, and signal transduction of primary rat hepatocytes. J. Cell. Biochem. 55, 445–464 (1994).
    Article CAS Google Scholar
  20. Gladhaug, I.P. & Christoffersen, T. Kinetics of epidermal growth factor binding and processing in isolated rat hepatocytes. Eur. J. Biochem. 164, 267–275 (1987).
    Article CAS Google Scholar
  21. Moriarity, D.M. & Savage, C.R. Interaction of epidermal growth factor with adult rat liver parenchymal cells in primary culture. Arch. Biochem. Biophys. 203, 506–518 (1980).
    Article CAS Google Scholar
  22. Wells, A. et al. Ligand-induced transformation by a non-internalizing growth factor. Science 247, 962–964 (1990).
    Article CAS Google Scholar
  23. Wiley, H.S., Walsh, B.J. & Lund, K.A. Global modulation of the epidermal growth factor receptor is triggered by occupancy of only a few receptors. J. Biol. Chem. 264, 912–918 (1989).
    Google Scholar
  24. Countaway, J.L., Nairn, A.C. & Davis, R.J. Mechanism of desensitization of the epidermal growth factor receptor protein-tyrosine kinase. J. Biol. Chem. 267, 1129–1140 (1992).
    CAS PubMed Google Scholar
  25. Stenger, D.A. et al Coplanar molecular assemblies of amino- and perfluorinated alkylsilanes: Characterization and geometric definition of mammalian cell adhesion and growth. J. Am. Chem. Soc. 114, 8435–8442 (1992).
    Article CAS Google Scholar
  26. Lopina, S.T., Wu, G., Merrill, E.W. & Griffith-Cima, L.G. Hepatocyte culture on carbohydrate-modified star polyethylene oxide hydrogels. Biomaterials 17, 559–569 (1996).
    Article CAS Google Scholar
  27. Lindroth, P. & Mopper, K. High performance liquid chromatographic determination of subpicomole amounts of amino acids by precolumn derivatization with O-phthaldialdehyde. Anal. Chem. 51, 1667–1674 (1979).
    Article CAS Google Scholar
  28. Cima, L.G., Ingber, D.E., Vacanti, J.P. & Langer, R. Hepatocyte culture on biodegradable polymeric substrates. Biotech. Bioeng. 38, 145–158 (1991).
    Article CAS Google Scholar

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