The Scribble Complex PDZ Proteins in Immune Cell Polarities

J Immunol Res. 2020 Apr 30:2020:5649790. doi: 10.1155/2020/5649790. eCollection 2020.

Abstract

hScrib and hDlg belong to the PDZ family of proteins. Since the identification of these highly phylogenetically conserved scaffolds, an increasing amount of experiments has elucidated the roles of hScrib and hDlg in a variety of cell functions. Remarkably, their participation during the establishment of polarity in epithelial cells is well documented. Although the role of both proteins in the immune system is scantly known, it has become a growing field of investigation. Here, we summarize the interactions and functions of hScrib and hDlg1, which participate in diverse functions involving cell polarization in immune cells, and discuss their relevance in the immune cell biology. The fundamental role of hScrib and hDlg1 during the establishment of the immunological synapse, hence T cell activation, and the recently described role of hScrib in reactive oxygen species production in macrophages and of hDlg1 in cytokine production by dendritic cells highlight the importance of both proteins in immune cell biology. The expression of these proteins in other leukocytes can be anticipated and needs to be confirmed. Due to their multiple interaction domains, there is a wide range of possible interactions of hScrib and hDlg1 that remains to be explored in the immune system.

Publication types

  • Review

MeSH terms

  • Cell Polarity / immunology*
  • Cytokines / metabolism
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Discs Large Homolog 1 Protein / metabolism*
  • Humans
  • Immunity, Cellular
  • Immunological Synapses / immunology
  • Immunological Synapses / metabolism
  • Lymphocyte Activation / immunology
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Membrane Proteins / metabolism*
  • Reactive Oxygen Species
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Cytokines
  • DLG1 protein, human
  • Discs Large Homolog 1 Protein
  • Membrane Proteins
  • Reactive Oxygen Species
  • SCRIB protein, human
  • Tumor Suppressor Proteins