Glycinergic inhibitory neurons of the spinal dorsal horn exert critical control over the conduction of nociceptive signals to higher brain areas. The neuronal glycine transporter 2 (GlyT2) is involved in the recycling of synaptic glycine from the inhibitory synaptic cleft and its activity modulates intra and extracellular glycine concentrations. In this report we show that the stimulation of P2X purinergic receptors with βγ-methylene adenosine 5'-triphosphate induces the up-regulation of GlyT2 transport activity by increasing total and plasma membrane expression and reducing transporter ubiquitination. We identified the receptor subtypes involved by combining pharmacological approaches, siRNA-mediated protein knockdown, and dorsal root ganglion cell enrichment in brainstem and spinal cord primary cultures. Up-regulation of GlyT2 required the combined stimulation of homomeric P2X3 and P2X2 receptors or heteromeric P2X2/3 receptors. We measured the spontaneous glycinergic currents, glycine release and GlyT2 uptake concurrently in response to P2X receptor agonists, and showed that the impact of P2X3 receptor activation on glycinergic neurotransmission involves the modulation of GlyT2 expression or activity. The recognized pro-nociceptive action of P2X3 receptors suggests that the fine-tuning of GlyT2 activity may have consequences in nociceptive signal conduction.
Keywords: 2-methylthio-adenosine-5′-triphosphate (PubChem CID: 107986); 2′,3′-O-(2,4,6-Trinitrophenyl) adenosine 5′-triphosphate (PubChem CID: 3035228); A317491 (PubChem CID 9829395); AF-353 (PubChem CID: 1595380); Hyperekplexia; MRS2179 (PubChem CID: 24867852); P2X; Pain; Purinergic; Transport; glycine; α,β-methylene adenosine 5′-triphosphate (PubChem CID:23702957); βγ-methylene adenosine 5′-triphosphate (PubChem CID:16219688).
Copyright © 2017 Elsevier Ltd. All rights reserved.