An Interleukin-17 Isoform from Thick Shell Mussel Serves as a Mediator of Inflammatory Response.

Molecules

National Engineering Research Center of Marine Facilities Aquaculture, Marine Science and Technology College, Zhejiang Ocean University, Zhoushan 316004, China.

Published: February 2023

The inflammatory cytokine interleukin-17 (IL17) plays an important role in innate immunity by binding to its receptors (IL17Rs) to activate immune defense signals. To date, information on members of the IL17 family is still very limited in molluscan species. Here, a novel member of the IL17 family was identified and characterized from thick shell mussel , and this gene was designated as IL17-1 by predicting structural domains and phylogenetic analysis. IL17-1 transcripts existed in all examined tissues with high expression levels in gills, hemocytes and digestive glands. After the stimuli of different pathogen associated molecular patterns (PAMPs) for 72 h, transcriptional expression of IL17-1 was significantly upregulated, except for poly I:C stimulation. Cytoplasm localization of IL17-1 was shown in HEK293T cells by fluorescence microscopy. Further, in vivo and in vitro assays were performed to evaluate the potential function of IL17-1 played in immune response. IL17-1 was either knocked down or overexpressed in vivo through RNA inference (RNAi) and recombinant protein injection, respectively. With the infection of living , a high mortality rate was exhibited in the IL17-1 overexpressed group compared to the control group, while a lower mortality rate was observed in the IL17-1 knocked down group than control group. In vitro, the flow cytometric analysis showed that the apoptosis rate of IL17-1 inhibited hemocytes was significantly lower than that of the control group after lipopolysaccharide stimulation. These results collectively suggested that the newly identified IL17 isoform is involved in the inflammatory response to bacterial infection in .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965057PMC
http://dx.doi.org/10.3390/molecules28041806DOI Listing

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