Publications

Journal Article Research Support, Non-U.S. Gov't Review Epublish 6 citations

PubMed: 34571930 DOI: 10.3390/cells10092282

P2X Receptor-Dependent Modulation of Mast Cell and Glial Cell Activities in Neuroinflammation.

Cells 10(9)

Authors: Barbora Salcman, Karen Affleck, Silvia Bulfone-Paus

Affiliations

  • Lydia Becker Institute of Immunology and Inflammation, Manchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M13 9NT, UK.
  • GlaxoSmithKline, Immunology Research Unit, Stevenage SG1 2NY, UK.

Abstract

Localisation of mast cells (MCs) at the abluminal side of blood vessels in the brain favours their interaction with glial cells, neurons, and endothelial cells, resulting in the activation of these cells and the release of pro-inflammatory mediators. In turn, stimulation of glial cells, such as microglia, astrocytes, and oligodendrocytes may result in the modulation of MC activities. MCs, microglia, astrocytes, and oligodendrocytes all express P2X receptors (P2XRs) family members that are selectively engaged by ATP. As increased concentrations of extracellular adenosine 5'-triphosphate (ATP) are present in the brain in neuropathological conditions, P2XR activation in MCs and glial cells contributes to the control of their communication and amplification of the inflammatory response. In this review we discuss P2XR-mediated MC activation, its bi-directional effect on microglia, astrocytes and oligodendrocytes and role in neuroinflammation.

MeSH

Brain, Mast Cells, Neuroglia, Astrocytes, Oligodendroglia, Microglia

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