Authors
Shuo Li, Shan Wang, Yao Zhang, Jiaying Wang, Jinsheng Sun
Published in
Fish & shellfish immunology. Pages 111679. Aug 24, 2026. Epub Aug 24, 2026.
Abstract
The A2b adenosine receptor (A2bR) is a critical modulator of inflammatory responses. Despite its high expression in Japanese flounder (Paralichthys olivaceus) macrophages, the expression characteristics and immunomodulatory functions of A2bR in this species remain poorly understood. Here, we molecularly characterized flounder A2bR and established its function as a potent negative regulator of teleost inflammation. The flounder A2bR gene displays an exon-intron architecture analogous to that of its mammalian orthologs and is broadly expressed across tissues, with maximal abundance in the skin. A2bR expression was induced by adenosine and significantly modulated by LPS stimulation in HKMs in vitro, as well as by Edwardsiella piscicida infection in vivo. Pharmacological activation of A2bR markedly attenuated the expression of proinflammatory cytokines and chemokines and reduced nitric oxide (NO) production, while concomitantly enhancing the expression of anti-inflammatory il-10 and the negative-feedback regulator socs1 in HKMs stimulated with LPS or poly(I:C). These immunosuppressive effects were recapitulated in A2bR-overexpressing flounder FG-9307 cells and murine RAW264.7 macrophages, underscoring an evolutionarily conserved function. Furthermore, A2bR activation significantly attenuated PAMP-induced pyroptosis-related gene expression in HKMs. Conversely, both pharmacological inhibition and siRNA-mediated knockdown of A2bR produced opposite effects. Collectively, we demonstrate for the first time in teleosts that A2bR orchestrates anti-inflammatory responses by suppressing the production of inflammatory mediator and the expression of proinflammatory genes, while promoting IL-10- and SOCS1-mediated negative feedback. These results suggest that A2bR is a promising target for modulating immune responses to infectious and inflammatory diseases in teleosts.
PMID:
42637162
Bibliographic data and abstract were imported from PubMed on 25 Aug 2026.
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