A Novel Forkhead Box Protein P (FoxP) From Litopenaeus vannamei Plays a Positive Role in Immune Response
Frontiers in Immunology, ISSN: 1664-3224, Vol: 11, Page: 593987
2020
- 6Citations
- 9Captures
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Metrics Details
- Citations6
- Citation Indexes6
- Captures9
- Readers9
Article Description
The forkhead box protein P (FoxP) family members have been known to be important for regulation of immune responses in vertebrates, but their roles in invertebrate immunity remain unclear. In this study, a novel FoxP gene (LvFoxP) was identified from Pacific white shrimp Litopenaeus vannamei and functionally studied in the context of immune response. Possessing a conserved FoxP coiled-coil domain and a forkhead domain, LvFoxP shared homology to vertebrate FoxP family members, in particular FoxP1. Expression of LvFoxP was detectable in all the examined tissues and could be up-regulated by immune challenge in gill and hemocytes. The LvFoxP protein was present in both the cytoplasm and nucleus of hemocytes and could be nuclear-translocated upon immune stimulation. Silencing of LvFoxP increased the susceptibility of shrimp to infections by Vibrio parahaemolyticus and white spot syndrome virus (WSSV) and down-regulated the expression of multiple components of NF-κB and JAK-STAT pathways and almost all the examined immune effector genes. Moreover, the phagocytic activity of hemocytes from LvFoxP-silenced shrimp against V. parahaemolyticus was decreased. These suggested that LvFoxP could play a positive role in immune response. The current study may provide novel insights into the immunity of invertebrates and the functional evolution of the FoxP family.
Bibliographic Details
10.3389/fimmu.2020.593987; 10.3389/fimmu.2020.593987.s004; 10.3389/fimmu.2020.593987.s005; 10.3389/fimmu.2020.593987.s003; 10.3389/fimmu.2020.593987.s002; 10.3389/fimmu.2020.593987.s001
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85098289920&origin=inward; http://dx.doi.org/10.3389/fimmu.2020.593987; http://www.ncbi.nlm.nih.gov/pubmed/33381114; https://www.frontiersin.org/articles/10.3389/fimmu.2020.593987/supplementary-material/10.3389/fimmu.2020.593987.s004; http://dx.doi.org/10.3389/fimmu.2020.593987.s004; https://www.frontiersin.org/articles/10.3389/fimmu.2020.593987/supplementary-material/10.3389/fimmu.2020.593987.s005; http://dx.doi.org/10.3389/fimmu.2020.593987.s005; https://www.frontiersin.org/articles/10.3389/fimmu.2020.593987/full; https://www.frontiersin.org/articles/10.3389/fimmu.2020.593987/supplementary-material/10.3389/fimmu.2020.593987.s003; http://dx.doi.org/10.3389/fimmu.2020.593987.s003; https://www.frontiersin.org/articles/10.3389/fimmu.2020.593987/supplementary-material/10.3389/fimmu.2020.593987.s002; http://dx.doi.org/10.3389/fimmu.2020.593987.s002; https://www.frontiersin.org/articles/10.3389/fimmu.2020.593987/supplementary-material/10.3389/fimmu.2020.593987.s001; http://dx.doi.org/10.3389/fimmu.2020.593987.s001; https://dx.doi.org/10.3389/fimmu.2020.593987; https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2020.593987/full; https://dx.doi.org/10.3389/fimmu.2020.593987.s005; https://dx.doi.org/10.3389/fimmu.2020.593987.s001; https://dx.doi.org/10.3389/fimmu.2020.593987.s003; https://dx.doi.org/10.3389/fimmu.2020.593987.s002; https://dx.doi.org/10.3389/fimmu.2020.593987.s004
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