Positive and Negative Signals in Mast Cell Activation

Trends Immunol. 2017 Sep;38(9):657-667. doi: 10.1016/j.it.2017.01.008. Epub 2017 Feb 20.

Abstract

Mast cells are powerful immune modulators of the tissue microenvironment. Within seconds of activation, these cells release a variety of preformed biologically active products, followed by a wave of mediator synthesis and secretion. Increasing evidence suggests that an intricate network of inhibitory and activating receptors, specific signaling pathways, and adaptor proteins governs mast cell responsiveness to stimuli. Here, we discuss the biological and clinical relevance of negative and positive signaling modalities that control mast cell activation, with an emphasis on novel FcεRI regulators, immunoglobulin E (IgE)-independent pathways [e.g., Mas-related G protein-coupled receptor X2 (MRGPRX2)], tetraspanins, and the CD300 family of inhibitory and activating receptors.

Publication types

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

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / metabolism
  • Cell Degranulation*
  • Ganglia, Spinal / metabolism
  • Humans
  • Immunomodulation
  • Ki-1 Antigen / metabolism
  • Mast Cells / immunology*
  • Nerve Tissue Proteins / metabolism*
  • Neuropeptides / metabolism
  • Receptors, G-Protein-Coupled / metabolism*
  • Receptors, IgE / metabolism
  • Receptors, Neuropeptide / metabolism*
  • Signal Transduction*
  • Tetraspanins / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • FCER1A protein, human
  • Ki-1 Antigen
  • MRGPRX2 protein, human
  • Nerve Tissue Proteins
  • Neuropeptides
  • Receptors, G-Protein-Coupled
  • Receptors, IgE
  • Receptors, Neuropeptide
  • Tetraspanins