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Sci. Signal., 7 April 2009
Vol. 2, Issue 65, p. ra15
[DOI: 10.1126/scisignal.2000199]
RESEARCH ARTICLES
Editor's Summary
Right Times and Right Places
Signals downstream of receptor activation can be effectively regulated by controlling both the distribution of signaling intermediates within the cell and the time at which they get to their destinations. Such spatiotemporal patterning of receptors, kinases, and adaptor molecules can have a substantial effect on their local concentrations and on the probabilities that they will interact with each other. Previous studies have characterized the patterning of individual or small groups of molecules; however, systems-level analyses of such processes are lacking. Singleton et al. have studied the spatiotemporal patterning of some 30 signaling intermediates in various mouse T cells activated by antigen-presenting cells under different conditions. As well as establishing that the patterning of these molecules regulates the efficiency of T cell receptor signaling, this study also shows that different T cell activation conditions generate different spatiotemporal patterns.
Citation: K. L. Singleton, K. T. Roybal, Y. Sun, G. Fu, N. R. J. Gascoigne, N. S. C. van Oers, C. Wülfing, Spatiotemporal Patterning During T Cell Activation Is Highly Diverse. Sci. Signal.2, ra15 (2009).
Kentner L. Singleton, Monica Gosh, Radhika D. Dandekar, Byron B. Au-Yeung, Olga Ksionda, Victor L. J. Tybulewicz, Amnon Altman, Deborah J. Fowell, and Christoph Wülfing (4 October 2011) Sci. Signal.4 (193), ra66.
[DOI: 10.1126/scisignal.2001821] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
Nuria Martínez-Martín, Ruth M. Risueño, Antonio Morreale, Irene Zaldívar, Elena Fernández-Arenas, Fernando Herranz, Angel R. Ortiz, and Balbino Alarcón (11 August 2009) Sci. Signal.2 (83), ra43.
[DOI: 10.1126/scisignal.2000402] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
EDITORIAL GUIDES
Nancy R. Gough and John F. Foley (28 July 2009) Sci. Signal.2 (81), eg10.
[DOI: 10.1126/scisignal.281eg10] |Abstract »|Full Text »|PDF »
EDITORS' CHOICE
John F. Foley (28 April 2009) Sci. Signal.2 (68), ec149.
[DOI: 10.1126/scisignal.268ec149] |Abstract »
M. Muscolini, C. Camperio, C. Capuano, S. Caristi, E. Piccolella, R. Galandrini, and L. Tuosto (2013)
J. Immunol.
190, 5279-5286
|Abstract »|Full Text »|PDF »
GRB2-Mediated Recruitment of THEMIS to LAT Is Essential for Thymocyte Development.
W. Paster, C. Brockmeyer, G. Fu, P. C. Simister, B. de Wet, A. Martinez-Riano, J. A. H. Hoerter, S. M. Feller, C. Wulfing, N. R. J. Gascoigne, et al. (2013)
J. Immunol.
190, 3749-3756
|Abstract »|Full Text »|PDF »
Mechanism and function of Vav1 localisation in TCR signalling.
O. Ksionda, A. Saveliev, R. Kochl, J. Rapley, M. Faroudi, J. E. Smith-Garvin, C. Wulfing, K. Rittinger, T. Carter, and V. L. J. Tybulewicz (2012)
J. Cell Sci.
125, 5302-5314
|Abstract »|Full Text »|PDF »
Multiple inhibitory ligands induce impaired T-cell immunologic synapse function in chronic lymphocytic leukemia that can be blocked with lenalidomide: establishing a reversible immune evasion mechanism in human cancer.
A. G. Ramsay, A. J. Clear, R. Fatah, and J. G. Gribben (2012)
Blood
120, 1412-1421
|Abstract »|Full Text »|PDF »
The myosin family: unconventional roles of actin-dependent molecular motors in immune cells.
J. L. Maravillas-Montero and L. Santos-Argumedo (2012)
J. Leukoc. Biol.
91, 35-46
|Abstract »|Full Text »|PDF »
Protein Kinase C {eta} Is Required for T Cell Activation and Homeostatic Proliferation.
G. Fu, J. Hu, N. Niederberger-Magnenat, V. Rybakin, J. Casas, P. P. Yachi, S. Feldstein, B. Ma, J. A. H. Hoerter, J. Ampudia, et al. (2011)
Science Signaling
4, ra84
|Abstract »|Full Text »|PDF »
Itk Controls the Spatiotemporal Organization of T Cell Activation.
K. L. Singleton, M. Gosh, R. D. Dandekar, B. B. Au-Yeung, O. Ksionda, V. L. J. Tybulewicz, A. Altman, D. J. Fowell, and C. Wulfing (2011)
Science Signaling
4, ra66
|Abstract »|Full Text »|PDF »
Myosin 1c Participates in B Cell Cytoskeleton Rearrangements, Is Recruited to the Immunologic Synapse, and Contributes to Antigen Presentation.
J. L. Maravillas-Montero, P. G. Gillespie, G. Patino-Lopez, S. Shaw, and L. Santos-Argumedo (2011)
J. Immunol.
187, 3053-3063
|Abstract »|Full Text »|PDF »
The CD3 {zeta} Subunit Contains a Phosphoinositide-Binding Motif That Is Required for the Stable Accumulation of TCR-CD3 Complex at the Immunological Synapse.
L. M. DeFord-Watts, D. S. Dougall, S. Belkaya, B. A. Johnson, J. L. Eitson, K. T. Roybal, B. Barylko, J. P. Albanesi, C. Wulfing, and N. S. C. van Oers (2011)
J. Immunol.
186, 6839-6847
|Abstract »|Full Text »|PDF »
Inhibiting the Inhibitor of the Inhibitor: Blocking PKC-{theta} to Enhance Regulatory T Cell Function.
Transience in polarization of cytolytic effectors is required for efficient killing and controlled by Cdc42.
P. Sinai, C. Nguyen, J. D. Schatzle, and C. Wulfing (2010)
PNAS
107, 11912-11917
|Abstract »|Full Text »|PDF »
Subcellular dynamics of T cell immunological synapses and kinapses in lymph nodes.
G. A. Azar, F. Lemaitre, E. A. Robey, and P. Bousso (2010)
PNAS
107, 3675-3680
|Abstract »|Full Text »|PDF »
Signalling complexes and clusters: functional advantages and methodological hurdles.
M. Cebecauer, M. Spitaler, A. Serge, and A. I. Magee (2010)
J. Cell Sci.
123, 309-320
|Abstract »|Full Text »|PDF »
The Cytoplasmic Tail of the T Cell Receptor CD3 {epsilon} Subunit Contains a Phospholipid-Binding Motif that Regulates T Cell Functions.
L. M. DeFord-Watts, T. C. Tassin, A. M. Becker, J. J. Medeiros, J. P. Albanesi, P. E. Love, C. Wulfing, and N. S. C. van Oers (2009)
J. Immunol.
183, 1055-1064
|Abstract »|Full Text »|PDF »