Ontology highlight
ABSTRACT: Introduction
Splenic B cells exhibit a high expression of the G protein-coupled sphingosine-1-phosphate (S1P) receptor type 4 (S1PR4). Little is known about the functional relevance of S1PR4 expression on those cells.Methods
In this study, S1PR4-deficient mice were used to study the role of S1PR4-mediated S1P signaling in B cell motility in vitro and for the maintenance of the splenic architecture under steady state conditions as well as in polymicrobial abdominal sepsis in vivo. Finally, the impact of S1PR4 deficiency on antibody production after immunization with T cell dependent antigens was assessed.Results
Loss of S1PR4 resulted in minor alterations of the splenic architecture conce
SUBMITTER: Riese J
PROVIDER: S-EPMC9755867 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature