B-cells are abnormal in psychosocial stress and regulate meningeal myeloid cell activation
Mary-Ellen Lynall, Stacey L. Kigar, Michael L. Lehmann, Allison E. DePuyt, Zewen Kelvin Tuong, Samuel J. Listwak, Abdel Elkahloun, Edward T. Bullmore, Miles Herkenham, Menna R. Clatworthy
Abstract
There is increasing interest in how immune cells, including those within the meninges at the blood–brain interface, influence brain function and mood disorders, but little data on humoral immunity in this context. Here, we show that in mice exposed to psychosocial stress, there is increased splenic B cell activation and secretion of the immunoregulatory cytokine interleukin (IL)-10. Meningeal B cells were prevalent in homeostasis but substantially decreased following stress, whereas Ly6Chi monocytes increased, and meningeal myeloid cells showed augmented expression of activation markers. Single-cell RNA sequencing of meningeal B cells demonstrated the induction of innate immune transcriptional programmes following stress, including genes encoding antimicrobial peptides that are known to alter myeloid cell activation. Cd19-/- mice, that have reduced B cells, showed baseline meningeal myeloid cell activation and decreased exploratory behaviour. Together, these data suggest that B cells may influence behaviour by regulating meningeal myeloid cell activation.