Protein Kinase C δ Regulates the Depletion of Actin at the Immunological Synapse Required for Polarized Exosome Secretion by T Cells

Front Immunol. 2019 Apr 26:10:851. doi: 10.3389/fimmu.2019.00851. eCollection 2019.

Abstract

Multivesicular bodies (MVB) are endocytic compartments that enclose intraluminal vesicles (ILVs) formed by inward budding from the limiting membrane of endosomes. In T lymphocytes, ILVs are secreted as Fas ligand-bearing, pro-apoptotic exosomes following T cell receptor (TCR)-induced fusion of MVB with the plasma membrane at the immune synapse (IS). In this study we show that protein kinase C δ (PKCδ), a novel PKC isotype activated by diacylglycerol (DAG), regulates TCR-controlled MVB polarization toward the IS and exosome secretion. Concomitantly, we demonstrate that PKCδ-interfered T lymphocytes are defective in activation-induced cell death. Using a DAG sensor based on the C1 DAG-binding domain of PKCδ and a GFP-PKCδ chimera, we reveal that T lymphocyte activation enhances DAG levels at the MVB endomembranes which mediates the association of PKCδ to MVB. Spatiotemporal reorganization of F-actin at the IS is inhibited in PKCδ-interfered T lymphocytes. Therefore, we propose PKCδ as a DAG effector that regulates the actin reorganization necessary for MVB traffic and exosome secretion.

Keywords: T lymphocytes; cell death; cytotoxic activity; exosomes; immune synapse; multivesicular bodies; protein kinase C δ.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism*
  • Apoptosis / immunology
  • Cell Line, Tumor
  • Cell Membrane / metabolism
  • Exosomes / metabolism*
  • Humans
  • Jurkat Cells
  • Lymphocyte Activation / immunology
  • Multivesicular Bodies / metabolism*
  • Protein Kinase C-delta / genetics
  • Protein Kinase C-delta / metabolism*
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Receptors, Antigen, T-Cell / metabolism
  • T-Lymphocytes / immunology*

Substances

  • Actins
  • RNA, Small Interfering
  • Receptors, Antigen, T-Cell
  • Protein Kinase C-delta