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        <identifier>oai:www.ideals.illinois.edu:2142/21284</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_5131</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Lauffenburger, Douglas A.</dc:contributor>
          <dc:creator>Reddy, Cartikeya Chennuru</dc:creator>
          <dc:date>2011-05-07T13:04:10Z</dc:date>
          <dc:date>2011-05-07T13:04:10Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1996</dc:date>
          <dc:description>At the present time, growth factor stimulation of cell proliferation is conceptualized predominantly in terms of the initial binding event between the growth factor and its receptor. However, the dynamics of the cellular trafficking of growth factors and their receptors can be an important determinant of the cellular response to growth factor stimulation. We have explored this hypothesis using the epidermal growth factor (EGF) receptor regulation of fibroblast proliferation as a model system. The mitogenic responses elicited by EGF, TGF$\alpha$, and an EGF-variant (Y13G) which possess different surface binding affinities and altered intracellular fates, are compared in distinct experimental scenarios, with or without ligand replenishment. Our results show that cellular uptake and trafficking of these ligands modulates the mitogenic response via a balance between receptor binding and concomitant mitogenic signaling from activated complexes, and the subsequent attenuation of signal due to internalization and degradation of growth factors and their receptors. Specifically, we have shown that Y13G, which has a binding affinity that is 50-fold lower than EGF and TGF$\alpha$, can be a better mitogen owing to its favorable trafficking properties. Therefore the relative potencies of these ligands cannot be predicted based on surface binding affinities alone. The dynamics of ligand and receptor accessibility as determined in conjunction with cellular properties and assay parameters are important determinants of growth factor potency.</dc:description>
          <dc:description>Our results demonstrate that ligand re-engineering--the optimization of the molecular interaction between growth factor and receptor--requires systemic integration of processes from the initial molecular recognition event to the ultimate cell response.</dc:description>
          <dc:description>Made available in DSpace on 2011-05-07T13:04:10Z (GMT). No. of bitstreams: 2
license.txt: 4922 bytes, checksum: 910b249b4beec47e7ab768910c8f966f (MD5)
9712416.pdf: 4970152 bytes, checksum: 29eb8eed174e6e84309653c99bd80a13 (MD5)
  Previous issue date: 1996</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:49:44Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:22:39-05:00
Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:identifier>9780591200454</dc:identifier>
          <dc:identifier>AAI9712416</dc:identifier>
          <dc:identifier>(UMI)AAI9712416</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/21284</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:rights>Copyright 1996 Reddy, Cartikeya Chennuru</dc:rights>
          <dc:subject>Biology, Cell</dc:subject>
          <dc:subject>Engineering, Biomedical</dc:subject>
          <dc:subject>Engineering, Chemical</dc:subject>
          <dc:title>Growth-factor-induced mitogenesis: Trafficking determinants of the cellular response</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Chemical and Biomolecular Engineering</department>
            <discipline>Chemical Engineering</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
        </thesis>
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