1. Academic Validation
  2. Suppression of caspase 8 activity by a coronin 1-PI3Kδ pathway promotes T cell survival independently of TCR and IL-7 signaling

Suppression of caspase 8 activity by a coronin 1-PI3Kδ pathway promotes T cell survival independently of TCR and IL-7 signaling

  • Sci Signal. 2021 Dec 21;14(714):eabj0057. doi: 10.1126/scisignal.abj0057.
Mayumi Mori 1 Julie Ruer-Laventie 1 Wandrille Duchemin 2 3 Philippe Demougin 4 Tohnyui Ndinyanka Fabrice 1 Matthias P Wymann 5 Jean Pieters 1
Affiliations

Affiliations

  • 1 Biozentrum, University of Basel, Basel, Switzerland.
  • 2 SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.
  • 3 Center for Scientific Computing (sciCORE), University of Basel, Basel, Switzerland.
  • 4 Biozentrum, Life Sciences Training Facility, University of Basel, Basel, Switzerland.
  • 5 Department of Biomedicine, University of Basel, Basel, Switzerland.
Abstract

The control of T cell survival is crucial for defense against infectious pathogens or emerging cancers. Although the survival of peripheral naïve T cells has been proposed to be controlled by interleukin-7 (IL-7) signaling and T cell receptor (TCR) activation by peptide-loaded major histocompatibility complexes (pMHC), the essential roles for these pathways in thymic output and T cell proliferation have complicated the analysis of their contributions to T cell survival. Here, we showed that the WD repeat–containing protein coronin 1, which is dispensable for thymic selection and output, promoted naïve T cell survival in the periphery in a manner that was independent of TCR and IL-7 signaling. Coronin 1 was required for the maintenance of the basal activity of phosphoinositide 3-kinase δ (PI3Kδ), thereby suppressing Caspase 8–mediated Apoptosis. These results therefore reveal a coronin 1–dependent PI3Kδ pathway that is independent of pMHC:TCR and IL-7 signaling and essential for peripheral T cell survival.

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