» Articles » PMID: 28421080

B Cell Functions Can Be Modulated by Antimicrobial Peptides in Rainbow Trout : Novel Insights into the Innate Nature of B Cells in Fish

Overview
Journal Front Immunol
Date 2017 Apr 20
PMID 28421080
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

B cells in fish were recently proven to have potent innate immune activities like macrophages. This inspired us to further explore the innate nature of B cells in fish. Moreover, antimicrobial peptides (AMPs) are representative molecules of innate immunity, and they can modulate the functions of macrophages. These make fish an appropriate model to study the interactions between B cells and AMPs. Interestingly, the results in this study revealed that the IgM and IgT B cells of rainbow trout could express multiple AMP genes, including four cathelicidin genes and one β-defensin gene. The expression levels of the cathelicidin genes were obviously higher than that of the β-defensin gene. Further studies revealed that intracellular, extracellular, , and stimulations could significantly increase the expression of the cathelicidin genes in trout IgM and IgT B cells but not the expression of the β-defensin gene, indicating that cathelicidin peptides are the main innate immune effectors of trout B cells. More interestingly, we found that cathelicidin peptides could significantly enhance the phagocytic, intracellular bactericidal, and reactive oxygen species activities of trout IgM and IgT B cells, a phenomenon previously reported only in macrophages, and these activities might also be mediated by the P2X receptor. These results collectively suggest that B cells play multiple roles in the innate immunity of fish, and they provide new evidence for understanding the close relationship between B cells and macrophages in vertebrates.

Citing Articles

Antibacterial Activity of Rainbow Trout Plasma: In Vitro Assays and Proteomic Analysis.

Mizaeva T, Alieva K, Zulkarneev E, Kurpe S, Isakova K, Matrosova S Animals (Basel). 2023; 13(22).

PMID: 38003182 PMC: 10668809. DOI: 10.3390/ani13223565.


Animal Models for the Investigation of P2X7 Receptors.

Sluyter R, Adriouch S, Fuller S, Nicke A, Sophocleous R, Watson D Int J Mol Sci. 2023; 24(9).

PMID: 37175933 PMC: 10179175. DOI: 10.3390/ijms24098225.


The dual antimicrobial and immunomodulatory roles of host defense peptides and their applications in animal production.

Wu D, Fu L, Wen W, Dong N J Anim Sci Biotechnol. 2022; 13(1):141.

PMID: 36474280 PMC: 9724304. DOI: 10.1186/s40104-022-00796-y.


Complement C3a Enhances the Phagocytic Activity of B Cells Through C3aR in a Fish.

Ma Z, Liang J, Li W, Sun Y, Wu C, Hu Y Front Immunol. 2022; 13:873982.

PMID: 35386704 PMC: 8977587. DOI: 10.3389/fimmu.2022.873982.


Salmonid Antibacterial Immunity: An Aquaculture Perspective.

Semple S, Dixon B Biology (Basel). 2020; 9(10).

PMID: 33050557 PMC: 7599743. DOI: 10.3390/biology9100331.


References
1.
Zhang Y, Salinas I, Li J, Parra D, Bjork S, Xu Z . IgT, a primitive immunoglobulin class specialized in mucosal immunity. Nat Immunol. 2010; 11(9):827-35. PMC: 3459821. DOI: 10.1038/ni.1913. View

2.
Boshra H, Wang T, Hove-Madsen L, Hansen J, Li J, Matlapudi A . Characterization of a C3a receptor in rainbow trout and Xenopus: the first identification of C3a receptors in nonmammalian species. J Immunol. 2005; 175(4):2427-37. DOI: 10.4049/jimmunol.175.4.2427. View

3.
Ruangsri J, Kitani Y, Kiron V, Lokesh J, Brinchmann M, Karlsen B . A novel beta-defensin antimicrobial peptide in Atlantic cod with stimulatory effect on phagocytic activity. PLoS One. 2013; 8(4):e62302. PMC: 3636224. DOI: 10.1371/journal.pone.0062302. View

4.
Chang C, Pleguezuelos O, Zhang Y, Zou J, Secombes C . Identification of a novel cathelicidin gene in the rainbow trout, Oncorhynchus mykiss. Infect Immun. 2005; 73(8):5053-64. PMC: 1201231. DOI: 10.1128/IAI.73.8.5053-5064.2005. View

5.
Abos B, Castro R, Gonzalez Granja A, Havixbeck J, Barreda D, Tafalla C . Early activation of teleost B cells in response to rhabdovirus infection. J Virol. 2014; 89(3):1768-80. PMC: 4300759. DOI: 10.1128/JVI.03080-14. View