Enterina JR, Sarkar S, Streith L, Jung J, Arlian BM, Meyer SJ, Takematsu H, Xiao C, Baldwin TA, Nitschke L, Shlomchick MJ, Paulson JC, Macauley MS (2022)
Publication Type: Journal article
Publication year: 2022
Book Volume: 38
Article Number: 110512
Journal Issue: 11
DOI: 10.1016/j.celrep.2022.110512
Germinal centers (GCs) are essential for antibody affinity maturation. GC B cells have a unique repertoire of cell surface glycans compared with naive B cells, yet functional roles for changes in glycosylation in the GC have yet to be ascribed. Detection of GCs by the antibody GL7 reflects a downregulation in ligands for CD22, an inhibitory co-receptor of the B cell receptor. To test a functional role for downregulation of CD22 ligands in the GC, we generate a mouse model that maintains CD22 ligands on GC B cells. With this model, we demonstrate that glycan remodeling plays a critical role in the maintenance of B cells in the GC. Sustained expression of CD22 ligands induces higher levels of apoptosis in GC B cells, reduces memory B cell and plasma cell output, and delays affinity maturation of antibodies. These defects are CD22 dependent, demonstrating that downregulation of CD22 ligands on B cells plays a critical function in the GC.
APA:
Enterina, J.R., Sarkar, S., Streith, L., Jung, J., Arlian, B.M., Meyer, S.J.,... Macauley, M.S. (2022). Coordinated changes in glycosylation regulate the germinal center through CD22. Cell Reports, 38(11). https://doi.org/10.1016/j.celrep.2022.110512
MLA:
Enterina, Jhon R., et al. "Coordinated changes in glycosylation regulate the germinal center through CD22." Cell Reports 38.11 (2022).
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