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Cutting edge: Regulation of T cell activation threshold by CD28 costimulation through targeting Cbl-b for ubiquitination

  • Jian Zhang
  • , Tamás Bárdos
  • , Dongdong Li
  • , István Gál
  • , Csaba Vermes
  • , Jianye Xu
  • , Katalin Mikecz
  • , Alison Finnegan
  • , Stan Lipkowitz
  • , Tibor T. Glant

Research output: Contribution to journalArticlepeer-review

Abstract

Optimal T cell activation requires signaling through the TCR and CD28 costimulatory receptor. CD28 costimulation is believed to set the threshold for T cell activation. Recently, Cbl-b, a ubiquitin ligase, has been shown to negatively regulate CD28-dependent T cell activation. In this report, we show that CD28 costimulation selectively induces greater ubiquitination and degradation of Cbl-b in wild-type T cells than CD3 stimulation alone, and TCR-induced Cbl-b ubiquitination and degradation are significantly reduced in CD28-deficient T cells. Stimulation of CD28-deficient T cells with higher doses of anti-CD3 results in increased ubiquitination of Cbl-b, which correlates with enhanced T cell responses. Our results demonstrate that CD28 costimulation regulates the threshold for T cell activation, at least in part, by promoting Cbl-b ubiquitination and degradation.

Original languageEnglish
Pages (from-to)2236-2240
Number of pages5
JournalJournal of Immunology
Volume169
Issue number5
DOIs
StatePublished - Sep 1 2002

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