TRAF3 regulates STAT6 activation and T-helper cell differentiation by modulating the phosphatase PTP1B.

ABSTRACT: The adaptor protein tumor necrosis factor receptor-associated factor 3 (TRAF3) is a multifaceted regulator of lymphocyte biology that plays key roles in modulation of the molecular signals required for T-cell activation and function. TRAF3 regulates signals mediated by the T-cell receptor (TCR), costimulatory molecules, and cytokine receptors, which each drive activation of the serine/threonine kinase Akt. The impact of TRAF3 upon TCR-CD28-mediated activation of Akt, and thus on the diverse cellular processes regulated by Akt, including CD4 T-cell fate decisions, remains poorly understood. We show here that TRAF3 deficiency led to impaired Akt activation and thus to impaired in vitro skewing of CD4 T cells into the T_H1 and T_H2 fates. We investigated the role of TRAF3

SUBMITTER: Arkee T 

PROVIDER: S-EPMC11462019 | biostudies-literature | 2024 Oct

REPOSITORIES: biostudies-literature