Essential role of ubiquitin and TSG101 protein in formation and function of the central supramolecular activation cluster. Academic Article uri icon

Overview

abstract

  • Agonist MHC-peptide complexes in the immunological synapse (IS) signal through T cell receptor (TCR) microclusters (MCs) that converge into a central supramolecular activation cluster (cSMAC). The determinants and function of the cSMAC remain unknown. We demonstrate an essential role for ubiquitin (Ub) and TSG101, but less so for HRS, in signal processing events at the cSMAC. Using siRNA in primary T cells, we show that Ub recognition by TSG101 is required for cSMAC formation, TCR MC signal termination, TCR downregulation, and segregation of TCR-MHC-peptide from PKC-theta-enriched signaling complexes. Weak agonist MHC-peptide induced CD80-dependent TCR MCs that dissociated in the center of the IS without recruiting TSG101. These results support TSG101-dependent recognition of CD80-independent TCR MCs as a molecular checkpoint for TCR downregulation.

publication date

  • April 23, 2010

Research

keywords

  • DNA-Binding Proteins
  • Endosomal Sorting Complexes Required for Transport
  • Immunological Synapses
  • Receptors, Antigen, T-Cell
  • T-Lymphocytes
  • Transcription Factors
  • Ubiquitin

Identity

PubMed Central ID

  • PMC2905630

Scopus Document Identifier

  • 77951688912

Digital Object Identifier (DOI)

  • 10.1016/j.immuni.2010.04.005

PubMed ID

  • 20399684

Additional Document Info

volume

  • 32

issue

  • 4