Abstract
Clustering of ligated integrins strongly influences integrin signaling and mechanical linkages between integrins and intracellular structures. Extracellular spatial organization of integrin ligands in clusters may facilitate clustering of bound integrins and thus potentially regulate cellular responses to a defined average amount of ligand in the extracellular environment. The possible role of such ligand clustering effects in controlling overall receptor occupancy is studied here using a simple mass-action equilibrium model as well as a two-dimensional Monte Carlo lattice description of the cell-substrate interface, where cell surface receptors are free to diffuse in the plane of the interface and interact with the substrate-immobilized ligand. Results from the analytical treatment and simulation data indicate that for a single-state model in which receptor-ligand binding equilibria are not influenced by neighboring complexes, clustering of ligand does not enhance total receptor binding. However, if receptor binding energy increases in the presence of neighboring ligated receptors, strong ligand spatial distribution effects arise. Nonlinear responses to increasing ligand density are also observed even in the case of random ligand placement due to stochastic juxtaposition of ligand molecules. These results describe how spatial distribution of ligand presented by the extracellular matrix or by synthetic biomimetic materials might control cell responses to external ligands, and suggest a feedback mechanism by which focal contact formation might be initiated.
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- Adams J. C. Cell-matrix contact structures. Cell Mol Life Sci. 2001 Mar;58(3):371–392. doi: 10.1007/PL00000864. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aplin A. E., Howe A., Alahari S. K., Juliano R. L. Signal transduction and signal modulation by cell adhesion receptors: the role of integrins, cadherins, immunoglobulin-cell adhesion molecules, and selectins. Pharmacol Rev. 1998 Jun;50(2):197–263. [PubMed] [Google Scholar]
- Aukhil I., Joshi P., Yan Y., Erickson H. P. Cell- and heparin-binding domains of the hexabrachion arm identified by tenascin expression proteins. J Biol Chem. 1993 Feb 5;268(4):2542–2553. [PubMed] [Google Scholar]
- Banerjee P., Irvine D. J., Mayes A. M., Griffith L. G. Polymer latexes for cell-resistant and cell-interactive surfaces. J Biomed Mater Res. 2000 Jun 5;50(3):331–339. doi: 10.1002/(sici)1097-4636(20000605)50:3<331::aid-jbm6>3.0.co;2-t. [DOI] [PubMed] [Google Scholar]
- Bell G. I., Dembo M., Bongrand P. Cell adhesion. Competition between nonspecific repulsion and specific bonding. Biophys J. 1984 Jun;45(6):1051–1064. doi: 10.1016/S0006-3495(84)84252-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burridge K., Chrzanowska-Wodnicka M. Focal adhesions, contractility, and signaling. Annu Rev Cell Dev Biol. 1996;12:463–518. doi: 10.1146/annurev.cellbio.12.1.463. [DOI] [PubMed] [Google Scholar]
- Chesla S. E., Selvaraj P., Zhu C. Measuring two-dimensional receptor-ligand binding kinetics by micropipette. Biophys J. 1998 Sep;75(3):1553–1572. doi: 10.1016/S0006-3495(98)74074-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chi-Rosso G., Gotwals P. J., Yang J., Ling L., Jiang K., Chao B., Baker D. P., Burkly L. C., Fawell S. E., Koteliansky V. E. Fibronectin type III repeats mediate RGD-independent adhesion and signaling through activated beta1 integrins. J Biol Chem. 1997 Dec 12;272(50):31447–31452. doi: 10.1074/jbc.272.50.31447. [DOI] [PubMed] [Google Scholar]
- Chothia C., Jones E. Y. The molecular structure of cell adhesion molecules. Annu Rev Biochem. 1997;66:823–862. doi: 10.1146/annurev.biochem.66.1.823. [DOI] [PubMed] [Google Scholar]
- Clark E. A., Brugge J. S. Integrins and signal transduction pathways: the road taken. Science. 1995 Apr 14;268(5208):233–239. doi: 10.1126/science.7716514. [DOI] [PubMed] [Google Scholar]
- Danen E. H., Aota S., van Kraats A. A., Yamada K. M., Ruiter D. J., van Muijen G. N. Requirement for the synergy site for cell adhesion to fibronectin depends on the activation state of integrin alpha 5 beta 1. J Biol Chem. 1995 Sep 15;270(37):21612–21618. doi: 10.1074/jbc.270.37.21612. [DOI] [PubMed] [Google Scholar]
- Danilov Y. N., Juliano R. L. (Arg-Gly-Asp)n-albumin conjugates as a model substratum for integrin-mediated cell adhesion. Exp Cell Res. 1989 May;182(1):186–196. doi: 10.1016/0014-4827(89)90290-5. [DOI] [PubMed] [Google Scholar]
- De Panfilis G., Ghidini A., Graifemberghi S., Barlati S., Zoppi N., Colombi M. Dexamethasone-induced healing of chronic leg ulcers in a patient with defective organization of the extracellular matrix of fibronectin. Br J Dermatol. 2000 Jan;142(1):166–170. doi: 10.1046/j.1365-2133.2000.03262.x. [DOI] [PubMed] [Google Scholar]
- Dembo M., Torney D. C., Saxman K., Hammer D. The reaction-limited kinetics of membrane-to-surface adhesion and detachment. Proc R Soc Lond B Biol Sci. 1988 Jun 22;234(1274):55–83. doi: 10.1098/rspb.1988.0038. [DOI] [PubMed] [Google Scholar]
- Duband J. L., Nuckolls G. H., Ishihara A., Hasegawa T., Yamada K. M., Thiery J. P., Jacobson K. Fibronectin receptor exhibits high lateral mobility in embryonic locomoting cells but is immobile in focal contacts and fibrillar streaks in stationary cells. J Cell Biol. 1988 Oct;107(4):1385–1396. doi: 10.1083/jcb.107.4.1385. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frelinger A. L., 3rd, Du X. P., Plow E. F., Ginsberg M. H. Monoclonal antibodies to ligand-occupied conformers of integrin alpha IIb beta 3 (glycoprotein IIb-IIIa) alter receptor affinity, specificity, and function. J Biol Chem. 1991 Sep 15;266(26):17106–17111. [PubMed] [Google Scholar]
- Friedl P., Bröcker E. B. The biology of cell locomotion within three-dimensional extracellular matrix. Cell Mol Life Sci. 2000 Jan 20;57(1):41–64. doi: 10.1007/s000180050498. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ginsberg M. H., Du X., Plow E. F. Inside-out integrin signalling. Curr Opin Cell Biol. 1992 Oct;4(5):766–771. doi: 10.1016/0955-0674(92)90099-x. [DOI] [PubMed] [Google Scholar]
- Hato T., Pampori N., Shattil S. J. Complementary roles for receptor clustering and conformational change in the adhesive and signaling functions of integrin alphaIIb beta3. J Cell Biol. 1998 Jun 29;141(7):1685–1695. doi: 10.1083/jcb.141.7.1685. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huttenlocher A., Ginsberg M. H., Horwitz A. F. Modulation of cell migration by integrin-mediated cytoskeletal linkages and ligand-binding affinity. J Cell Biol. 1996 Sep;134(6):1551–1562. doi: 10.1083/jcb.134.6.1551. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hynes R. O. Cell adhesion: old and new questions. Trends Cell Biol. 1999 Dec;9(12):M33–M37. [PubMed] [Google Scholar]
- Hynes R. O., Yamada K. M. Fibronectins: multifunctional modular glycoproteins. J Cell Biol. 1982 Nov;95(2 Pt 1):369–377. doi: 10.1083/jcb.95.2.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Irvine D. J., Mayes A. M., Griffith L. G. Nanoscale clustering of RGD peptides at surfaces using Comb polymers. 1. Synthesis and characterization of Comb thin films. Biomacromolecules. 2001 Spring;2(1):85–94. doi: 10.1021/bm005584b. [DOI] [PubMed] [Google Scholar]
- Knight B., Laukaitis C., Akhtar N., Hotchin N. A., Edlund M., Horwitz A. R. Visualizing muscle cell migration in situ. Curr Biol. 2000 May 18;10(10):576–585. doi: 10.1016/s0960-9822(00)00486-3. [DOI] [PubMed] [Google Scholar]
- Kornberg L. J., Earp H. S., Turner C. E., Prockop C., Juliano R. L. Signal transduction by integrins: increased protein tyrosine phosphorylation caused by clustering of beta 1 integrins. Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8392–8396. doi: 10.1073/pnas.88.19.8392. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LaFlamme S. E., Akiyama S. K., Yamada K. M. Regulation of fibronectin receptor distribution. J Cell Biol. 1992 Apr;117(2):437–447. doi: 10.1083/jcb.117.2.437. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lauffenburger D. A., Horwitz A. F. Cell migration: a physically integrated molecular process. Cell. 1996 Feb 9;84(3):359–369. doi: 10.1016/s0092-8674(00)81280-5. [DOI] [PubMed] [Google Scholar]
- Lotz M. M., Burdsal C. A., Erickson H. P., McClay D. R. Cell adhesion to fibronectin and tenascin: quantitative measurements of initial binding and subsequent strengthening response. J Cell Biol. 1989 Oct;109(4 Pt 1):1795–1805. doi: 10.1083/jcb.109.4.1795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maheshwari G., Brown G., Lauffenburger D. A., Wells A., Griffith L. G. Cell adhesion and motility depend on nanoscale RGD clustering. J Cell Sci. 2000 May;113(Pt 10):1677–1686. doi: 10.1242/jcs.113.10.1677. [DOI] [PubMed] [Google Scholar]
- Massia S. P., Hubbell J. A. An RGD spacing of 440 nm is sufficient for integrin alpha V beta 3-mediated fibroblast spreading and 140 nm for focal contact and stress fiber formation. J Cell Biol. 1991 Sep;114(5):1089–1100. doi: 10.1083/jcb.114.5.1089. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miyamoto S., Akiyama S. K., Yamada K. M. Synergistic roles for receptor occupancy and aggregation in integrin transmembrane function. Science. 1995 Feb 10;267(5199):883–885. doi: 10.1126/science.7846531. [DOI] [PubMed] [Google Scholar]
- Miyamoto S., Teramoto H., Coso O. A., Gutkind J. S., Burbelo P. D., Akiyama S. K., Yamada K. M. Integrin function: molecular hierarchies of cytoskeletal and signaling molecules. J Cell Biol. 1995 Nov;131(3):791–805. doi: 10.1083/jcb.131.3.791. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miyamoto S., Teramoto H., Gutkind J. S., Yamada K. M. Integrins can collaborate with growth factors for phosphorylation of receptor tyrosine kinases and MAP kinase activation: roles of integrin aggregation and occupancy of receptors. J Cell Biol. 1996 Dec;135(6 Pt 1):1633–1642. doi: 10.1083/jcb.135.6.1633. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nomizu M., Kuratomi Y., Malinda K. M., Song S. Y., Miyoshi K., Otaka A., Powell S. K., Hoffman M. P., Kleinman H. K., Yamada Y. Cell binding sequences in mouse laminin alpha1 chain. J Biol Chem. 1998 Dec 4;273(49):32491–32499. doi: 10.1074/jbc.273.49.32491. [DOI] [PubMed] [Google Scholar]
- Oh E. S., Woods A., Couchman J. R. Multimerization of the cytoplasmic domain of syndecan-4 is required for its ability to activate protein kinase C. J Biol Chem. 1997 May 2;272(18):11805–11811. doi: 10.1074/jbc.272.18.11805. [DOI] [PubMed] [Google Scholar]
- Pelham R. J., Jr, Wang Y. l. Cell locomotion and focal adhesions are regulated by substrate flexibility. Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):13661–13665. doi: 10.1073/pnas.94.25.13661. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Piper J. W., Swerlick R. A., Zhu C. Determining force dependence of two-dimensional receptor-ligand binding affinity by centrifugation. Biophys J. 1998 Jan;74(1):492–513. doi: 10.1016/S0006-3495(98)77807-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ruoslahti E. RGD and other recognition sequences for integrins. Annu Rev Cell Dev Biol. 1996;12:697–715. doi: 10.1146/annurev.cellbio.12.1.697. [DOI] [PubMed] [Google Scholar]
- Schmidt C. E., Horwitz A. F., Lauffenburger D. A., Sheetz M. P. Integrin-cytoskeletal interactions in migrating fibroblasts are dynamic, asymmetric, and regulated. J Cell Biol. 1993 Nov;123(4):977–991. doi: 10.1083/jcb.123.4.977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Segel L. A., Volk T., Geiger B. On spatial periodicity in the formation of cell adhesions to a substrate. Cell Biophys. 1983 Jun;5(2):95–104. doi: 10.1007/BF02796136. [DOI] [PubMed] [Google Scholar]
- Shaw L. M., Messier J. M., Mercurio A. M. The activation dependent adhesion of macrophages to laminin involves cytoskeletal anchoring and phosphorylation of the alpha 6 beta 1 integrin. J Cell Biol. 1990 Jun;110(6):2167–2174. doi: 10.1083/jcb.110.6.2167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spring J., Beck K., Chiquet-Ehrismann R. Two contrary functions of tenascin: dissection of the active sites by recombinant tenascin fragments. Cell. 1989 Oct 20;59(2):325–334. doi: 10.1016/0092-8674(89)90294-8. [DOI] [PubMed] [Google Scholar]
- Ward M. D., Hammer D. A. A theoretical analysis for the effect of focal contact formation on cell-substrate attachment strength. Biophys J. 1993 Mar;64(3):936–959. doi: 10.1016/S0006-3495(93)81456-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ward M. D., Hammer D. A. Focal contact assembly through cytoskeletal polymerization: steady state analysis. J Math Biol. 1994;32(7):677–704. doi: 10.1007/BF00163022. [DOI] [PubMed] [Google Scholar]
- Wary K. K., Mariotti A., Zurzolo C., Giancotti F. G. A requirement for caveolin-1 and associated kinase Fyn in integrin signaling and anchorage-dependent cell growth. Cell. 1998 Sep 4;94(5):625–634. doi: 10.1016/s0092-8674(00)81604-9. [DOI] [PubMed] [Google Scholar]
- Weber P. C., Ohlendorf D. H., Wendoloski J. J., Salemme F. R. Structural origins of high-affinity biotin binding to streptavidin. Science. 1989 Jan 6;243(4887):85–88. doi: 10.1126/science.2911722. [DOI] [PubMed] [Google Scholar]
- Wei Y., Yang X., Liu Q., Wilkins J. A., Chapman H. A. A role for caveolin and the urokinase receptor in integrin-mediated adhesion and signaling. J Cell Biol. 1999 Mar 22;144(6):1285–1294. doi: 10.1083/jcb.144.6.1285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xiao Y., Truskey G. A. Effect of receptor-ligand affinity on the strength of endothelial cell adhesion. Biophys J. 1996 Nov;71(5):2869–2884. doi: 10.1016/S0006-3495(96)79484-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xie H., Pallero M. A., Gupta K., Chang P., Ware M. F., Witke W., Kwiatkowski D. J., Lauffenburger D. A., Murphy-Ullrich J. E., Wells A. EGF receptor regulation of cell motility: EGF induces disassembly of focal adhesions independently of the motility-associated PLCgamma signaling pathway. J Cell Sci. 1998 Mar;111(Pt 5):615–624. doi: 10.1242/jcs.111.5.615. [DOI] [PubMed] [Google Scholar]
- Yamada K. M., Aota S., Akiyama S. K., LaFlamme S. E. Mechanisms of fibronectin and integrin function during cell adhesion and migration. Cold Spring Harb Symp Quant Biol. 1992;57:203–212. doi: 10.1101/sqb.1992.057.01.025. [DOI] [PubMed] [Google Scholar]
- Yauch R. L., Felsenfeld D. P., Kraeft S. K., Chen L. B., Sheetz M. P., Hemler M. E. Mutational evidence for control of cell adhesion through integrin diffusion/clustering, independent of ligand binding. J Exp Med. 1997 Oct 20;186(8):1347–1355. doi: 10.1084/jem.186.8.1347. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zamir E., Katz B. Z., Aota S., Yamada K. M., Geiger B., Kam Z. Molecular diversity of cell-matrix adhesions. J Cell Sci. 1999 Jun;112(Pt 11):1655–1669. doi: 10.1242/jcs.112.11.1655. [DOI] [PubMed] [Google Scholar]