Abstract
B-1 and B-2 B cell populations have different progenitors, receptor diversity, anatomic location, and functions-suggesting vastly differing requisites for homeostatic regulation. There is evidence that the B lymphocyte stimulator (BLyS) family of cytokines and receptors, key factors in the homeostatic regulation of B-2 B cell subsets, is also a major player in the B-1 compartment. Here we review the development and differentiation of these two primary B cell lineages and their immune functions. We discuss evidence that BLyS or a proliferation-inducing ligand (APRIL) availability in different anatomic sites, coupled with signature BLyS receptor expression patterns on different B cell subsets, may be important for homeostatic regulation of B-1 as well as B-2 populations. Finally, we extend our working model of B cell homeostasis to integrate B-1s. © 2013 Sindhava, Scholz and Cancro.
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Sindhava, V. J., Scholz, J. L., & Cancro, M. P. (2013). Roles for BLyS family members in meeting the distinct homeostatic demands of innate and adaptive B cells. Frontiers in Immunology. https://doi.org/10.3389/fimmu.2013.00037
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