Ezrin tunes T‐cell activation by controlling Dlg1 and microtubule positioning at the immunological synapse

T‐cell receptor (TCR) signalling is triggered and tuned at immunological synapses by the generation of signalling complexes that associate into dynamic microclusters. Microcluster movement is necessary to tune TCR signalling, but the molecular mechanism involved remains poorly known. We show here that the membrane‐microfilament linker ezrin has an important function in microcluster dynamics and in TCR signalling through its ability to set the microtubule network organization at the immunological synapse. Importantly, ezrin and microtubules are important to down‐regulate signalling events leading to Erk1/2 activation. In addition, ezrin is required for appropriate NF‐AT activation through p38 MAP kinase. Our data strongly support the notion that ezrin regulates immune synapse architecture and T‐cell activation through its interaction with the scaffold protein Dlg1. These results uncover a crucial function for ezrin, Dlg1 and microtubules in the organization of the immune synapse and TCR signal down‐regulation. Moreover, they underscore the importance of ezrin and Dlg1 in the regulation of NF‐AT activation through p38.

[1]  Min Zhang,et al.  Dlgh1 coordinates actin polymerization, synaptic T cell receptor and lipid raft aggregation, and effector function in T cells , 2005, The Journal of experimental medicine.

[2]  S. Bunnell,et al.  T cell costimulation via the integrin VLA-4 inhibits the actin-dependent centralization of signaling microclusters containing the adaptor SLP-76. , 2008, Immunity.

[3]  M. Smyth,et al.  A network of PDZ-containing proteins regulates T cell polarity and morphology during migration and immunological synapse formation. , 2005, Immunity.

[4]  A. Dautry‐Varsat,et al.  Human immunodeficiency virus type-1 infection impairs the formation of the immunological synapse. , 2006, Immunity.

[5]  Michael Loran Dustin T‐cell activation through immunological synapses and kinapses , 2008, Immunological reviews.

[6]  A. Trautmann,et al.  ERM proteins regulate cytoskeleton relaxation promoting T cell–APC conjugation , 2004, Nature Immunology.

[7]  R. Germain,et al.  Exclusion of CD43 from the immunological synapse is mediated by phosphorylation-regulated relocation of the cytoskeletal adaptor moesin. , 2001, Immunity.

[8]  R. Schneider,et al.  Arginine methylation of the B cell antigen receptor promotes differentiation , 2010, The Journal of experimental medicine.

[9]  S. Aresta,et al.  Interaction of ezrin with the novel guanine nucleotide exchange factor PLEKHG6 promotes RhoG-dependent apical cytoskeleton rearrangements in epithelial cells. , 2007, Molecular biology of the cell.

[10]  J. Girault,et al.  Ezrin Interacts with Focal Adhesion Kinase and Induces Its Activation Independently of Cell-matrix Adhesion* , 2001, The Journal of Biological Chemistry.

[11]  Rajat Varma,et al.  T cell receptor-proximal signals are sustained in peripheral microclusters and terminated in the central supramolecular activation cluster. , 2006, Immunity.

[12]  J. Burkhardt,et al.  The actin cytoskeleton in T cell activation. , 2008, Annual review of immunology.

[13]  María Yáñez-Mó,et al.  ITAM-based interaction of ERM proteins with Syk mediates signaling by the leukocyte adhesion receptor PSGL-1. , 2002, Immunity.

[14]  Takashi Saito,et al.  Newly generated T cell receptor microclusters initiate and sustain T cell activation by recruitment of Zap70 and SLP-76 , 2005, Nature Immunology.

[15]  K. Mossman,et al.  Altered TCR Signaling from Geometrically Repatterned Immunological Synapses , 2005, Science.

[16]  A. Weiss,et al.  Uncoupling of nonreceptor tyrosine kinases from PLC-gamma1 in an SLP-76-deficient T cell. , 1998, Science.

[17]  U. Landegren,et al.  Protein detection using proximity-dependent DNA ligation assays , 2002, Nature Biotechnology.

[18]  D. Branton,et al.  Two independent domains of hDlg are sufficient for subcellular targeting: the PDZ1-2 conformational unit and an alternatively spliced domain , 1996, The Journal of cell biology.

[19]  M. Arpin,et al.  ERM proteins in epithelial cell organization and functions. , 2007, Biochimica et biophysica acta.

[20]  A. Chakraborty,et al.  The balance between T cell receptor signaling and degradation at the center of the immunological synapse is determined by antigen quality. , 2008, Immunity.

[21]  B. Freedman,et al.  Ezrin and Moesin Function Together to Promote T Cell Activation1 , 2009, The Journal of Immunology.

[22]  A. Bretscher,et al.  Immune synapse formation requires ZAP-70 recruitment by ezrin and CD43 removal by moesin , 2007, The Journal of cell biology.

[23]  A. Kupfer,et al.  TCR signaling induces selective exclusion of CD43 from the T cell-antigen-presenting cell contact site. , 1998, Journal of immunology.

[24]  Min Zhang,et al.  Scaffold protein Dlgh1 coordinates alternative p38 kinase activation, directing T cell receptor signals toward NFAT but not NF-κB transcription factors , 2007, Nature Immunology.

[25]  A. Gautreau,et al.  Ezrin regulates E-cadherin-dependent adherens junction assembly through Rac1 activation. , 2003, Molecular biology of the cell.

[26]  Kenneth G. Johnson,et al.  Polar Redistribution of the Sialoglycoprotein CD43: Implications for T Cell Function1 , 2002, The Journal of Immunology.

[27]  C. Reverdy,et al.  Spatial recruitment and activation of the Fes kinase by ezrin promotes HGF‐induced cell scattering , 2008, The EMBO journal.

[28]  Oreste Acuto,et al.  Tailoring T-cell receptor signals by proximal negative feedback mechanisms , 2008, Nature Reviews Immunology.

[29]  Tetsuo Yamazaki,et al.  T cell receptor ligation induces the formation of dynamically regulated signaling assemblies , 2002, The Journal of cell biology.

[30]  Christian Roy,et al.  Phosphoinositide binding and phosphorylation act sequentially in the activation mechanism of ezrin , 2004, The Journal of cell biology.

[31]  S. Takahashi,et al.  ERM-dependent movement of CD43 defines a novel protein complex distal to the immunological synapse. , 2001, Immunity.

[32]  Jean-Christophe Olivo-Marin,et al.  Extraction of spots in biological images using multiscale products , 2002, Pattern Recognit..

[33]  A. Bruckbauer,et al.  The Membrane Skeleton Controls Diffusion Dynamics and Signaling through the B Cell Receptor , 2010, Immunity.

[34]  U. Landegren,et al.  Direct observation of individual endogenous protein complexes in situ by proximity ligation , 2006, Nature Methods.

[35]  R. Nossal,et al.  T‐Cell Antigen Receptor‐Induced Signaling Complexes: Internalization Via a Cholesterol‐Dependent Endocytic Pathway , 2006, Traffic.

[36]  M. Poenie,et al.  Dynamic polarization of the microtubule cytoskeleton during CTL-mediated killing. , 2002, Immunity.

[37]  A. Mammoto,et al.  Direct Interaction of the Rho GDP Dissociation Inhibitor with Ezrin/Radixin/Moesin Initiates the Activation of the Rho Small G Protein* , 1997, The Journal of Biological Chemistry.

[38]  Michael Loran Dustin,et al.  Spatiotemporal regulation of T cell costimulation by TCR-CD28 microclusters and protein kinase C theta translocation. , 2008, Immunity.

[39]  J. Olivo-Marin,et al.  The membrane-microfilament linker ezrin is involved in the formation of the immunological synapse and in T cell activation. , 2001, Immunity.

[40]  James Monypenny,et al.  Ezrin is a downstream effector of trafficking PKC–integrin complexes involved in the control of cell motility , 2001, The EMBO journal.

[41]  A. Echard,et al.  Moesin and its activating kinase Slik are required for cortical stability and microtubule organization in mitotic cells , 2008, The Journal of cell biology.

[42]  A. Bretscher,et al.  T cell antigen receptor signaling and immunological synapse stability require myosin IIA , 2009, Nature Immunology.

[43]  Shigemi Kinoshita,et al.  Activation of the PKB/AKT pathway by ICAM-2. , 2002, Immunity.

[44]  K. Shokat,et al.  HIV-1 Nef assembles a Src family kinase-ZAP-70/Syk-PI3K cascade to downregulate cell-surface MHC-I. , 2007, Cell host & microbe.

[45]  C. Carlson,et al.  Inhibition of T Cell Activation by Cyclic Adenosine 5′-Monophosphate Requires Lipid Raft Targeting of Protein Kinase A Type I by the A-Kinase Anchoring Protein Ezrin1 , 2007, The Journal of Immunology.

[46]  Andrew E. Pelling,et al.  Moesin Controls Cortical Rigidity, Cell Rounding, and Spindle Morphogenesis during Mitosis , 2008, Current Biology.

[47]  Andrea I. McClatchey,et al.  Organizing the cell cortex: the role of ERM proteins , 2010, Nature Reviews Molecular Cell Biology.

[48]  Rajat Varma,et al.  Actin and agonist MHC–peptide complex–dependent T cell receptor microclusters as scaffolds for signaling , 2005, The Journal of experimental medicine.

[49]  A. Alcover,et al.  Role of ERM (ezrin-radixin-moesin) proteins in T lymphocyte polarization, immune synapse formation and in T cell receptor-mediated signaling. , 2006, Frontiers in bioscience : a journal and virtual library.

[50]  David G. Morris,et al.  Discs large (Dlg1) complexes in lymphocyte activation , 2004, The Journal of cell biology.