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Cutting Edge: Redox Signaling Hypersensitivity Distinguishes Human Germinal Center B Cells
Author(s) -
Hannah G. Polikowsky,
Cara E Wogsland,
Kirsten E. Diggins,
Kanutte Huse,
Jonathan M. Irish
Publication year - 2015
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1500904
Subject(s) - germinal center , breakpoint cluster region , flow cytometry , syk , microbiology and biotechnology , phosphorylation , cd40 , b cell , biology , signal transduction , chemistry , immunology , antibody , biochemistry , in vitro , receptor , cytotoxic t cell , tyrosine kinase
Differences in the quality of BCR signaling control key steps of B cell maturation and differentiation. Endogenously produced H2O2 is thought to fine tune the level of BCR signaling by reversibly inhibiting phosphatases. However, relatively little is known about how B cells at different stages sense and respond to such redox cues. In this study, we used phospho-specific flow cytometry and high-dimensional mass cytometry (CyTOF) to compare BCR signaling responses in mature human tonsillar B cells undergoing germinal center (GC) reactions. GC B cells, in contrast to mature naive B cells, memory B cells, and plasmablasts, were hypersensitive to a range of H2O2 concentrations and responded by phosphorylating SYK and other membrane-proximal BCR effectors in the absence of BCR engagement. These findings reveal that stage-specific redox responses distinguish human GC B cells.

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