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Astrocytic and Oligodendrocytic P2X7 Receptors Determine Neuronal Functions in the CNS

Journal

FRONTIERS IN MOLECULAR NEUROSCIENCE
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnmol.2021.641570

Keywords

astrocytes; oligodendrocytes; neurons; signaling molecules

Categories

Funding

  1. National Key R&D Program of China [2019YFC1709101]
  2. Project First-Class Disciplines Development of Chengdu University of Traditional Chinese Medicine [CZYHW1901]
  3. Science and Technology Program of Sichuan Province, China [2019YFH0108]
  4. State Administration of Foreign Experts Affairs [G20190236012]

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P2X7 receptors are mainly found in microglial cells in the brain, with lower density in neuroglial cells, involved in regulating necrosis/apoptosis and neurodegenerative processes. The question of whether they are present on neurons and the potential existence of neuronal P2X7Rs remains a topic of debate.
P2X7 receptors are members of the ATP-gated cationic channel family with a preferential localization at the microglial cells, the resident macrophages of the brain. However, these receptors are also present at neuroglia (astrocytes, oligodendrocytes) although at a considerably lower density. They mediate necrosis/apoptosis by the release of pro-inflammatory cytokines/chemokines, reactive oxygen species (ROS) as well as the excitotoxic (glio)transmitters glutamate and ATP. Besides mediating cell damage i.e., superimposed upon chronic neurodegenerative processes in Alzheimer's Disease, Parkinson's Disease, multiple sclerosis, and amyotrophic lateral sclerosis, they may also participate in neuroglial signaling to neurons under conditions of high ATP concentrations during any other form of neuroinflammation/neurodegeneration. It is a pertinent open question whether P2X7Rs are localized on neurons, or whether only neuroglia/microglia possess this receptor-type causing indirect effects by releasing the above-mentioned signaling molecules. We suggest as based on molecular biology and functional evidence that neurons are devoid of P2X7Rs although the existence of neuronal P2X7Rs cannot be excluded with absolute certainty.

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