Dissociation of actin polymerization and lipid raft accumulation by ligation of the Inducible Costimulator (ICOS, CD278)

No abstract is available for this paper.

• Publication year

  2012

• Venue

  Inmunología

• Publication date

  Unknown publication date

• Fields of study

  Biology, Chemistry

• Identifiers
  DOI 10.1016/J.INMUNO.2011.06.002
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Biased binding of class IA phosphatidyl inositol 3-kinase subunits to inducible costimulator (CD278)

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  2010cited by this paper
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  2010cited by this paper
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• p85beta phosphoinositide 3-kinase regulates CD28 coreceptor function.

  2009cited by this paper
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• Loss of N-terminal Charged Residues of Mouse CD3ϵ Chains Generates Isoforms Modulating Antigen T Cell Receptor-mediated Signals and T Cell Receptor-CD3 Interactions*

  2007cited by this paper
• CTL-Associated Antigen-4 Ligation Induces Rapid T Cell Polarization That Depends on Phosphatidylinositol 3-Kinase, Vav-1, Cdc42, and Myosin Light Chain Kinase1

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• Regulation of T-cell activation by the cytoskeleton

  2007cited by this paper
• Plasma membrane-associated proteins are clustered into islands attached to the cytoskeleton

  2006cited by this paper
• CD28 interaction with filamin-A controls lipid raft accumulation at the T-cell immunological synapse

  2006cited by this paper
• AILIM/ICOS-mediated elongation of activated T cells is regulated by both the PI3-kinase/Akt and Rho family cascade.

  2006cited by this paper
• Lipid rafts and regulation of the cytoskeleton during T cell activation

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• Hierarchical Regulation of CTLA-4 Dimer-Based Lattice Formation and Its Biological Relevance for T Cell Inactivation1

  2005cited by this paper
• Ligation of CD28 by Its Natural Ligand CD86 in the Absence of TCR Stimulation Induces Lipid Raft Polarization in Human CD4 T Cells1

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• Monoclonal antibodies to murine CD3 epsilon define distinct epitopes, one of which may interact with CD4 during T cell activation.

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  1979cited by this paper

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