Abstract
The serial engagement model provides an attractive and plausible explanation for how a typical antigen presenting cell, exhibiting a low density of peptides recognized by a T cell, can initiate T cell responses. If a single peptide displayed by a major histocompatibility complex (MHC) can bind, sequentially, to different T cell receptors (TCR), then a few peptides can activate many receptors. To date, arguments supporting and questioning the prevalence of serial engagement have centered on the down-regulation of TCR after contact of T cells with antigen presenting cells. Recently, the existence of serial engagement has been challenged by the demonstration that engagement of TCR can down-regulate nonengaged bystander TCR. Here we show that for binding and dissociation rates that characterize interactions between T cell receptors and peptide-MHC, substantial serial engagement occurs. The result is independent of mechanisms and measurements of receptor down-regulation. The conclusion that single peptide-MHC engage many TCR, before diffusing out of the contact region between the antigen-presenting cell and the T cell, is based on a general first passage time calculation for a particle alternating between states in which different diffusion coefficients govern its transport.
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Selected References
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- Bachmann M. F., Ohashi P. S. The role of T-cell receptor dimerization in T-cell activation. Immunol Today. 1999 Dec;20(12):568–576. doi: 10.1016/s0167-5699(99)01543-1. [DOI] [PubMed] [Google Scholar]
- Bachmann M. F., Salzmann M., Oxenius A., Ohashi P. S. Formation of TCR dimers/trimers as a crucial step for T cell activation. Eur J Immunol. 1998 Aug;28(8):2571–2579. doi: 10.1002/(SICI)1521-4141(199808)28:08<2571::AID-IMMU2571>3.0.CO;2-T. [DOI] [PubMed] [Google Scholar]
- Boniface J. J., Rabinowitz J. D., Wülfing C., Hampl J., Reich Z., Altman J. D., Kantor R. M., Beeson C., McConnell H. M., Davis M. M. Initiation of signal transduction through the T cell receptor requires the multivalent engagement of peptide/MHC ligands [corrected]. Immunity. 1998 Oct;9(4):459–466. doi: 10.1016/s1074-7613(00)80629-9. [DOI] [PubMed] [Google Scholar]
- Corr M., Slanetz A. E., Boyd L. F., Jelonek M. T., Khilko S., al-Ramadi B. K., Kim Y. S., Maher S. E., Bothwell A. L., Margulies D. H. T cell receptor-MHC class I peptide interactions: affinity, kinetics, and specificity. Science. 1994 Aug 12;265(5174):946–949. doi: 10.1126/science.8052850. [DOI] [PubMed] [Google Scholar]
- Davis M. M., Boniface J. J., Reich Z., Lyons D., Hampl J., Arden B., Chien Y. Ligand recognition by alpha beta T cell receptors. Annu Rev Immunol. 1998;16:523–544. doi: 10.1146/annurev.immunol.16.1.523. [DOI] [PubMed] [Google Scholar]
- Dustin M. L. Adhesive bond dynamics in contacts between T lymphocytes and glass-supported planar bilayers reconstituted with the immunoglobulin-related adhesion molecule CD58. J Biol Chem. 1997 Jun 20;272(25):15782–15788. doi: 10.1074/jbc.272.25.15782. [DOI] [PubMed] [Google Scholar]
- Dustin M. L., Ferguson L. M., Chan P. Y., Springer T. A., Golan D. E. Visualization of CD2 interaction with LFA-3 and determination of the two-dimensional dissociation constant for adhesion receptors in a contact area. J Cell Biol. 1996 Feb;132(3):465–474. doi: 10.1083/jcb.132.3.465. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Edidin M., Kuo S. C., Sheetz M. P. Lateral movements of membrane glycoproteins restricted by dynamic cytoplasmic barriers. Science. 1991 Nov 29;254(5036):1379–1382. doi: 10.1126/science.1835798. [DOI] [PubMed] [Google Scholar]
- Garcia K. C., Scott C. A., Brunmark A., Carbone F. R., Peterson P. A., Wilson I. A., Teyton L. CD8 enhances formation of stable T-cell receptor/MHC class I molecule complexes. Nature. 1996 Dec 12;384(6609):577–581. doi: 10.1038/384577a0. [DOI] [PubMed] [Google Scholar]
- Germain R. N., Stefanová I. The dynamics of T cell receptor signaling: complex orchestration and the key roles of tempo and cooperation. Annu Rev Immunol. 1999;17:467–522. doi: 10.1146/annurev.immunol.17.1.467. [DOI] [PubMed] [Google Scholar]
- Goldstein B., Griego R., Wofsy C. Diffusion-limited forward rate constants in two dimensions. Application to the trapping of cell surface receptors by coated pits. Biophys J. 1984 Nov;46(5):573–586. doi: 10.1016/S0006-3495(84)84056-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grakoui A., Bromley S. K., Sumen C., Davis M. M., Shaw A. S., Allen P. M., Dustin M. L. The immunological synapse: a molecular machine controlling T cell activation. Science. 1999 Jul 9;285(5425):221–227. doi: 10.1126/science.285.5425.221. [DOI] [PubMed] [Google Scholar]
- Itoh Y., Hemmer B., Martin R., Germain R. N. Serial TCR engagement and down-modulation by peptide:MHC molecule ligands: relationship to the quality of individual TCR signaling events. J Immunol. 1999 Feb 15;162(4):2073–2080. [PubMed] [Google Scholar]
- Kersh G. J., Kersh E. N., Fremont D. H., Allen P. M. High- and low-potency ligands with similar affinities for the TCR: the importance of kinetics in TCR signaling. Immunity. 1998 Dec;9(6):817–826. doi: 10.1016/s1074-7613(00)80647-0. [DOI] [PubMed] [Google Scholar]
- Lanzavecchia A., Iezzi G., Viola A. From TCR engagement to T cell activation: a kinetic view of T cell behavior. Cell. 1999 Jan 8;96(1):1–4. doi: 10.1016/s0092-8674(00)80952-6. [DOI] [PubMed] [Google Scholar]
- Lanzavecchia A., Sallusto F. From synapses to immunological memory: the role of sustained T cell stimulation. Curr Opin Immunol. 2000 Feb;12(1):92–98. doi: 10.1016/s0952-7915(99)00056-4. [DOI] [PubMed] [Google Scholar]
- Lyons D. S., Lieberman S. A., Hampl J., Boniface J. J., Chien Y., Berg L. J., Davis M. M. A TCR binds to antagonist ligands with lower affinities and faster dissociation rates than to agonists. Immunity. 1996 Jul;5(1):53–61. doi: 10.1016/s1074-7613(00)80309-x. [DOI] [PubMed] [Google Scholar]
- Matsui K., Boniface J. J., Steffner P., Reay P. A., Davis M. M. Kinetics of T-cell receptor binding to peptide/I-Ek complexes: correlation of the dissociation rate with T-cell responsiveness. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12862–12866. doi: 10.1073/pnas.91.26.12862. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McKeithan T. W. Kinetic proofreading in T-cell receptor signal transduction. Proc Natl Acad Sci U S A. 1995 May 23;92(11):5042–5046. doi: 10.1073/pnas.92.11.5042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Munnelly H. M., Brady C. J., Hagen G. M., Wade W. F., Roess D. A., Barisas B. G. Rotational and lateral dynamics of I-A(k) molecules expressing cytoplasmic truncations. Int Immunol. 2000 Sep;12(9):1319–1328. doi: 10.1093/intimm/12.9.1319. [DOI] [PubMed] [Google Scholar]
- Niedergang F., Dautry-Varsat A., Alcover A. Peptide antigen or superantigen-induced down-regulation of TCRs involves both stimulated and unstimulated receptors. J Immunol. 1997 Aug 15;159(4):1703–1710. [PubMed] [Google Scholar]
- O'Shea J. J. Jaks, STATs, cytokine signal transduction, and immunoregulation: are we there yet? Immunity. 1997 Jul;7(1):1–11. doi: 10.1016/s1074-7613(00)80505-1. [DOI] [PubMed] [Google Scholar]
- Qiu Y., Wade W. F., Roess D. A., Barisas B. G. Lateral dynamics of major histocompatibility complex class II molecules bound with agonist peptide or altered peptide ligands. Immunol Lett. 1996 Oct;53(1):19–23. doi: 10.1016/0165-2478(96)02607-7. [DOI] [PubMed] [Google Scholar]
- San José E., Borroto A., Niedergang F., Alcover A., Alarcón B. Triggering the TCR complex causes the downregulation of nonengaged receptors by a signal transduction-dependent mechanism. Immunity. 2000 Feb;12(2):161–170. doi: 10.1016/s1074-7613(00)80169-7. [DOI] [PubMed] [Google Scholar]
- Saxton M. J., Jacobson K. Single-particle tracking: applications to membrane dynamics. Annu Rev Biophys Biomol Struct. 1997;26:373–399. doi: 10.1146/annurev.biophys.26.1.373. [DOI] [PubMed] [Google Scholar]
- Shaw A. S., Dustin M. L. Making the T cell receptor go the distance: a topological view of T cell activation. Immunity. 1997 Apr;6(4):361–369. doi: 10.1016/s1074-7613(00)80279-4. [DOI] [PubMed] [Google Scholar]
- Torigoe C., Goldstein B., Wofsy C., Metzger H. Shuttling of initiating kinase between discrete aggregates of the high affinity receptor for IgE regulates the cellular response. Proc Natl Acad Sci U S A. 1997 Feb 18;94(4):1372–1377. doi: 10.1073/pnas.94.4.1372. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Torigoe C., Inman J. K., Metzger H. An unusual mechanism for ligand antagonism. Science. 1998 Jul 24;281(5376):568–572. doi: 10.1126/science.281.5376.568. [DOI] [PubMed] [Google Scholar]
- Valitutti S., Müller S., Cella M., Padovan E., Lanzavecchia A. Serial triggering of many T-cell receptors by a few peptide-MHC complexes. Nature. 1995 May 11;375(6527):148–151. doi: 10.1038/375148a0. [DOI] [PubMed] [Google Scholar]
- Wade W. F., Freed J. H., Edidin M. Translational diffusion of class II major histocompatibility complex molecules is constrained by their cytoplasmic domains. J Cell Biol. 1989 Dec;109(6 Pt 2):3325–3331. doi: 10.1083/jcb.109.6.3325. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wofsy C., Torigoe C., Kent U. M., Metzger H., Goldstein B. Exploiting the difference between intrinsic and extrinsic kinases: implications for regulation of signaling by immunoreceptors. J Immunol. 1997 Dec 15;159(12):5984–5992. [PubMed] [Google Scholar]
- Wülfing C., Davis M. M. A receptor/cytoskeletal movement triggered by costimulation during T cell activation. Science. 1998 Dec 18;282(5397):2266–2269. doi: 10.1126/science.282.5397.2266. [DOI] [PubMed] [Google Scholar]