Identification of IL-40, a Novel B Cell-Associated Cytokine.
Jovani Catalan-DibeneMonica I VazquezVan Phi LuuSean-Paul NuccioAlborz KarimzadehJenna M KastenschmidtS Armando VillaltaIrina UshachEgest J PonePaolo CasaliManuela RaffatelluAmanda M BurkhardtMarcela Hernandez-RuizGina HellerPeter A HeveziAlbert ZlotnikPublished in: Journal of immunology (Baltimore, Md. : 1950) (2017)
We describe a novel B cell-associated cytokine, encoded by an uncharacterized gene (C17orf99; chromosome 17 open reading frame 99), that is expressed in bone marrow and fetal liver and whose expression is also induced in peripheral B cells upon activation. C17orf99 is only present in mammalian genomes, and it encodes a small (∼27-kDa) secreted protein unrelated to other cytokine families, suggesting a function in mammalian immune responses. Accordingly, C17orf99 expression is induced in the mammary gland upon the onset of lactation, and a C17orf99-/- mouse exhibits reduced levels of IgA in the serum, gut, feces, and lactating mammary gland. C17orf99-/- mice have smaller and fewer Peyer's patches and lower numbers of IgA-secreting cells. The microbiome of C17orf99-/- mice exhibits altered composition, likely a consequence of the reduced levels of IgA in the gut. Although naive B cells can express C17orf99 upon activation, their production increases following culture with various cytokines, including IL-4 and TGF-β1, suggesting that differentiation can result in the expansion of C17orf99-producing B cells during some immune responses. Taken together, these observations indicate that C17orf99 encodes a novel B cell-associated cytokine, which we have called IL-40, that plays an important role in humoral immune responses and may also play a role in B cell development. Importantly, IL-40 is also expressed by human activated B cells and by several human B cell lymphomas. The latter observations suggest that it may play a role in the pathogenesis of certain human diseases.
Keyphrases
- immune response
- endothelial cells
- bone marrow
- high glucose
- induced pluripotent stem cells
- diabetic rats
- pluripotent stem cells
- induced apoptosis
- binding protein
- dendritic cells
- gene expression
- drug induced
- dna methylation
- minimally invasive
- copy number
- working memory
- hiv infected
- epithelial mesenchymal transition
- heat shock protein
- signaling pathway
- stress induced