Teleost IgD+IgM− B cells in gills and skin have a plasmablast profile, but functionally and phenotypically differ from IgM+IgD− B cells in these sites
J. Germán Herranz-Jusdado,
Esther Morel,
Rocío Simón,
Patricia Díaz-Rosales,
Carolina Tafalla
Affiliations
J. Germán Herranz-Jusdado
Animal Health Research Center (CISA), Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Consejo Superior de Investigaciones Científicas (CSIC), Valdeolmos 28130 Madrid, Spain
Esther Morel
Animal Health Research Center (CISA), Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Consejo Superior de Investigaciones Científicas (CSIC), Valdeolmos 28130 Madrid, Spain
Rocío Simón
Animal Health Research Center (CISA), Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Consejo Superior de Investigaciones Científicas (CSIC), Valdeolmos 28130 Madrid, Spain
Patricia Díaz-Rosales
Animal Health Research Center (CISA), Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Consejo Superior de Investigaciones Científicas (CSIC), Valdeolmos 28130 Madrid, Spain
Carolina Tafalla
Animal Health Research Center (CISA), Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Consejo Superior de Investigaciones Científicas (CSIC), Valdeolmos 28130 Madrid, Spain; Corresponding author
Summary: Although most B cells in teleost systemic compartments co-express IgM and IgD on the surface, cells exclusively expressing either of the two Igs are common in fish mucosal tissues, providing us with a unique opportunity to further characterize IgD+IgM− B cells, an intriguing B cell subset. Hence, we compared the phenotype of IgD+IgM− cells to that of IgM+IgD− B cells in rainbow trout gills and skin, also establishing the response of these subsets to immune stimulation. The transcriptional profile and secreting capacity of IgD+IgM− B cells corresponded to that of cells that have started a differentiation program toward plasmablasts, similarly to IgM+IgD− B cells. Yet, IgM+IgD− B cells retained high levels of surface MHC II and antigen-processing abilities, while these were much lower in IgD+IgM− cells, suggesting important differences in their antigen-presenting capacities. Our findings contribute to a deeper understanding of the enigmatic role of IgD in mucosal surfaces.