Drebrin 1 in dendritic cells regulates phagocytosis and cell surface receptor expression through recycling for efficient antigen presentation

Immunology. 2019 Feb;156(2):136-146. doi: 10.1111/imm.13010. Epub 2018 Nov 8.

Abstract

Phagocytosis, macropinocytosis and antigen presentation by dendritic cells (DC) requires reorganization of the actin cytoskeleton. Drebrin (Dbn1) is an actin binding and stabilizing protein with roles in endocytosis, formation of dendrite spines in neurons and coordinating cell-cell synapses in immune cells. However, its role in DC phagocytosis and antigen presentation is unknown. These studies now report that silencing of Dbn1 in DC resulted in restrained cell surface display of receptors, most notably MHC class I and II and co-stimulatory molecules. This, as expected, resulted in impaired antigen-specific T-cell activation and proliferation. Studies additionally revealed that knockdown of Dbn1 in DC impaired macropinocytosis and phagocytosis. However, there was a concomitant increase in fluid-phase uptake, suggesting that Dbn1 is responsible for the differential control of macropinocytosis versus micropinocytosis activities. Taken together, these findings now reveal that Dbn1 plays a major role in coordinating the actin cytoskeletal activities responsible for antigen presentation in DC.

Keywords: actin bundling; actin cytoskeleton; dendritic cells; endocytosis; innate immunity; phagocytosis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antigen Presentation*
  • Cytoskeleton / genetics
  • Cytoskeleton / immunology
  • Dendritic Cells / cytology
  • Dendritic Cells / immunology*
  • Gene Expression Regulation / immunology*
  • Gene Knockout Techniques
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology*
  • Histocompatibility Antigens Class II / genetics
  • Histocompatibility Antigens Class II / immunology*
  • Immunological Synapses / genetics
  • Immunological Synapses / immunology
  • Lymphocyte Activation / genetics
  • Mice
  • Mice, Transgenic
  • Neuropeptides / genetics
  • Neuropeptides / immunology*
  • Phagocytosis*
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology

Substances

  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Neuropeptides
  • drebrins