DOK3 is involved in microglial cell activation in neuropathic pain by interacting with GPR84.

Abstract

Adaptor molecule downstream of kinase-3 (DOK3) is a vital regulator of innate immune responses in macrophages and B cells, and G-protein-coupled receptor 84 (GPR84) is significant in mediating the biosynthesis and maintenance of inflammatory mediators that are induced by neuropathic pain in microglia. In the present study, we determined the role of DOK3 in activating microglia-induced neuropathic pain and investigated the underlying mechanisms associated with GPR84. We found that knockdown of DOK3 in microglial cells dramatically reduced the levels of inflammatory factors, and we uncovered a physical association between DOK3 and GPR84 in the induction of inflammatory responses. We also observed that neuropathic pain and inflammatory responses induced by chronic constriction injury (CCI) of the sciatic nerve or intrathecal injection of a GPR84 agonist were compromised in DOK3-/- mice in vivo. Finally, enforced expression of DOK3 provoked inflammatory responses, and administration of pregabalin relieved neuropathic pain via inhibition of DOK3 expression. In conclusion, DOK3 induced neuropathic pain in mice by interacting with GPR84 in microglia. We hypothesize that targeting the adaptor protein DOK3 may open new avenues for pharmaceutical approaches to the alleviation of neuropathic pain in the spinal cord.

• Authors: Wen-Shuang Gao, Yu-Juan Qu, Juan Huai, Hui Wei, Yang Zhang, Shou-Wei Yue
• Journal: Aging (Aging (Albany NY)) Vol. 13 Issue 1 Pg. 389-410 (12 03 2020) ISSN: 1945-4589 [Electronic] United States
• PMID: 33281117 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Adaptor Proteins, Signal Transducing
• Analgesics
• Dok3 protein, mouse
• Gpr84 protein, mouse
• Receptors, G-Protein-Coupled
• Pregabalin

Topics

• Adaptor Proteins, Signal Transducing (drug effects, genetics, metabolism)
• Analgesics (pharmacology)
• Animals
• Cell Line
• Gene Knockdown Techniques
• Inflammation
• Mice
• Mice, Knockout
• Microglia (immunology, metabolism)
• Neuralgia (genetics, immunology, metabolism)
• Pregabalin (pharmacology)
• Receptors, G-Protein-Coupled (agonists, metabolism)
• Sciatic Nerve (injuries)