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Updated: Jul 10, 2026

Teasing Out the Interplay Between Natural Killer Cells and Nociceptor Neurons
Published on: June 30, 2022
Regulation of nociceptin/orphaninFQ secretion by immune cells and functional modulation of interleukin-2
Thomas R Miller1, Allison J Fulford
1Department of Anatomy, University of Bristol, Southwell Street, Bristol, UK.
Abstract:
Previous research has demonstrated that numerous populations of immune cell, including lymphocytes, synthesize nociceptin (N/OFQ) precursor mRNA although little is known regarding the immunological role of N/OFQ. In the present study we have demonstrated significant effects of mitogens, pro-inflammatory cytokines, cyclic AMP analogues, glucocorticoids and CRF on N/OFQ secretion by rat splenocytes in vitro. N/OFQ (10(-14) to 10(-10)M) was also shown to inhibit proliferation of Con A-activated splenocytes and production of IL-2 in vitro. In summary we have shown how a variety of stimuli relevant to inflammation can regulate endogenous N/OFQ secretion by splenocytes in vitro. We also suggest that N/OFQ may promote anti-inflammatory actions via suppression of IL-2 in vivo.
Insights
Immune cells, including lymphocytes, produce nociceptin (N/OFQ). This study shows N/OFQ regulates immune cell function and may possess anti-inflammatory effects by suppressing Interleukin-2 (IL-2) production.
Area of Science:
- Immunology
- Neuroendocrinology
- Molecular Biology
Background:
- Immune cells, such as lymphocytes, synthesize nociceptin (N/OFQ) precursor mRNA.
- The precise immunological functions of N/OFQ remain largely unexplored.
Purpose of the Study:
- To investigate the regulation of N/OFQ secretion by immune cells.
- To determine the effects of N/OFQ on immune cell proliferation and cytokine production.
Main Methods:
- Rat splenocytes were cultured in vitro.
- N/OFQ secretion was measured following stimulation with mitogens, pro-inflammatory cytokines, cyclic AMP analogues, glucocorticoids, and CRF.
- The impact of N/OFQ on Concanavalin A (Con A)-activated splenocyte proliferation and Interleukin-2 (IL-2) production was assessed.
Main Results:
- Mitogens, pro-inflammatory cytokines, cyclic AMP analogues, glucocorticoids, and CRF significantly affected N/OFQ secretion by rat splenocytes in vitro.
- N/OFQ inhibited the proliferation of Con A-activated splenocytes.
- N/OFQ suppressed the production of IL-2 in vitro.
Conclusions:
- Inflammatory stimuli can modulate endogenous N/OFQ secretion by splenocytes.
- N/OFQ may exert anti-inflammatory actions by suppressing IL-2 production in vivo.
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