Miller Thomas R, Fulford Allison J
Department of Anatomy, University of Bristol, Southwell Street, Bristol, UK.
Peptides. 2007 Nov;28(11):2243-52. doi: 10.1016/j.peptides.2007.09.004. Epub 2007 Sep 15.
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.
先前的研究表明,包括淋巴细胞在内的众多免疫细胞群体均可合成孤啡肽(N/OFQ)前体mRNA,尽管人们对N/OFQ的免疫作用知之甚少。在本研究中,我们已证明丝裂原、促炎细胞因子、环磷酸腺苷类似物、糖皮质激素和促肾上腺皮质激素释放因子对体外培养的大鼠脾细胞分泌N/OFQ具有显著影响。N/OFQ(10^(-14)至10^(-10)M)在体外也显示出可抑制刀豆蛋白A激活的脾细胞增殖及白细胞介素-2的产生。总之,我们已表明多种与炎症相关的刺激如何在体外调节脾细胞内源性N/OFQ的分泌。我们还认为,N/OFQ可能通过在体内抑制白细胞介素-2来促进抗炎作用。