The neutral sphingomyelinase 2 in T cell receptor signaling and polarity

Biol Chem. 2018 Sep 25;399(10):1147-1155. doi: 10.1515/hsz-2017-0280.

Abstract

By hydrolyzing its substrate sphingomyelin at the cytosolic leaflet of cellular membranes, the neutral sphingomyelinase 2 (NSM2) generates microdomains which serve as docking sites for signaling proteins and thereby, functions to regulate signal relay. This has been particularly studied in cellular stress responses while the regulatory role of this enzyme in the immune cell compartment has only recently emerged. In T cells, phenotypic polarization by co-ordinated cytoskeletal remodeling is central to motility and interaction with endothelial or antigen-presenting cells during tissue recruitment or immune synapse formation, respectively. This review highlights studies adressing the role of NSM2 in T cell polarity in which the enzyme plays a major role in regulating cytoskeletal dynamics.

Keywords: T cell; neutral sphingomyelinase; polarity; signaling.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Polarity*
  • Humans
  • Receptors, Antigen, T-Cell / immunology*
  • Signal Transduction
  • Sphingomyelin Phosphodiesterase / metabolism*
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Receptors, Antigen, T-Cell
  • SMPD3 protein, human
  • Smpd3 protein, mouse
  • Sphingomyelin Phosphodiesterase