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Adenosine A3 agonists reverse neuropathic pain via T cell–mediated production of IL-10
Mariaconcetta Durante, … , Kenneth A. Jacobson, Daniela Salvemini
Mariaconcetta Durante, … , Kenneth A. Jacobson, Daniela Salvemini
Published February 23, 2021
Citation Information: J Clin Invest. 2021;131(7):e139299. https://doi.org/10.1172/JCI139299.
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Concise Communication Neuroscience Therapeutics

Adenosine A3 agonists reverse neuropathic pain via T cell–mediated production of IL-10

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Abstract

The A3 adenosine receptor (A3AR) has emerged as a therapeutic target with A3AR agonists to tackle the global challenge of neuropathic pain, and investigation into its mode of action is essential for ongoing clinical development. Immune cell A3ARs, and their activation during pathology, modulate cytokine release. Thus, the use of immune cells as a cellular substrate for the pharmacological action of A3AR agonists is enticing, but unknown. The present study discovered that Rag-KO mice lacking T and B cells, as compared with WT mice, are insensitive to the anti-allodynic effects of A3AR agonists. Similar findings were observed in interleukin-10 and interleukin-10 receptor knockout mice. Adoptive transfer of CD4+ T cells from WT mice infiltrated the dorsal root ganglion (DRG) and restored A3AR agonist-mediated anti-allodynia in Rag-KO mice. CD4+ T cells from Adora3-KO or Il10-KO mice did not. Transfer of CD4+ T cells from WT mice, but not Il10-KO mice, into Il10-KO mice or Adora3-KO mice fully reinstated the anti-allodynic effects of A3AR activation. Notably, A3AR agonism reduced DRG neuron excitability when cocultured with CD4+ T cells in an IL-10–dependent manner. A3AR action on CD4+ T cells infiltrated in the DRG decreased phosphorylation of GluN2B-containing N-methyl-D-aspartate receptors at Tyr1472, a modification associated with regulating neuronal hypersensitivity. Our findings establish that activation of A3AR on CD4+ T cells to release IL-10 is required and sufficient evidence for the use of A3AR agonists as therapeutics.

Authors

Mariaconcetta Durante, Silvia Squillace, Filomena Lauro, Luigino Antonio Giancotti, Elisabetta Coppi, Federica Cherchi, Lorenzo Di Cesare Mannelli, Carla Ghelardini, Grant Kolar, Carrie Wahlman, Adeleye Opejin, Cuiying Xiao, Marc L. Reitman, Dilip K. Tosh, Daniel Hawiger, Kenneth A. Jacobson, Daniela Salvemini

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Figure 4

IL-10 released by CD4+ T cells is required for A3AR agonist–mediated inhibition of AP firing in cocultured mouse DRG neurons isolated from naive mice.

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IL-10 released by CD4+ T cells is required for A3AR agonist–mediated inh...
Original current-clamp traces recorded by whole-cell patch-clamp technique in typical mouse DRG neurons. AP firing was evoked by a depolarizing ramp current injection (1 second; 30 pA; lower inset) once every 30 seconds. The A3AR agonist MRS5980 (300 nM) was applied in (A) DRG-CD4+ T cell cocultures, (D) DRG-CD4+ T cell cocultures in the presence of anti-IL-10 antibody (Ab IL-10; 0.5 μg/ml), (G) DRG-CD8+ T cell cocultures, and (J) DRG cultures. The number of APs elicited by the current ramp was plotted as a function of time in 4 different representative cells (B, E, H, and K) or was expressed as pooled data (mean ± SEM) in the bar graphs (L, n = 6; C, n = 10; F, n = 11; I, n = 7). Dotted gray lines indicate the 0 mV level. *P = 0.0120, paired Student’s t test. The number of APs elicited before MRS5980 application (with bars, ctrl) was not different in DRG neurons cultured alone (L), DRG neurons cocultured with CD4+ T cells (C), DRG neurons cocultured with CD4+ T cells in the presence of anti-IL-10 antibody (F), or DRG neurons cocultured with CD8+ T cells (I). One-way ANOVA with Bonferroni comparison: L vs C: P = 0.3981; C vs. F: P = 0.1034; L vs. F: P > 0.9999; L vs. I: P > 0.9999. Scale bars: 300 ms; 50 mV.

Copyright © 2021 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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