Abstract
B cell development is a highly regulated process that initiates in the bone marrow (BM) of adult mice. After reaching the IgM+ immature stage in the BM, these B cells migrate to the spleen to complete maturation and incorporation into the long-lived peripheral lymphocyte pool. Studies have identified these splenic immature B cells, and have further attempted to delineate the sequence whereby they transition into mature B cells. As such, these immature splenic populations are termed transitional B cells and have been the focus of intense study. The review summarizes the phenotype and currently known functions of the four putative transitional B cell subsets identified to date. Although most appear to represent short-lived transitional B cells, the CD21hi T2 B cell population exhibits a number of qualities that question its label as a transitional B cell subset.
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Acknowledgments
The authors wish to acknowledge the technical assistance of Teresa Duling, Gene Hess and Lorraine Tygrett, and the contribution of autoimmune mice by Dr. Polly Ferguson.
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Verma, S., Waldschmidt, T.J. Characterization of splenic CD21hi T2 B cells. Immunol Res 39, 240–248 (2007). https://doi.org/10.1007/s12026-007-0072-5
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DOI: https://doi.org/10.1007/s12026-007-0072-5