B220 is a lineage associated– rather than an activation marker in the NK-cell differentiation pathway and defines pre-mNK cells. Guimont-Desrochers et al adoptively transferred various NK-cell subsets and followed their proliferation and phenotype in immunocompetent versus Rag1-deficient recipients treated or not with activating stimuli (known to up-regulate B220 molecules in vitro). While IKDCs remained B220 at early time points without activation (and maintained this expression at later time points after activation), B220− NK cells (expressing or not CD27) failed to acquire B220. The follow-up study of B220+ NK cells revealed that this subset differentiated into maturing NK cells over time, losing B220, Ly108, and CD27 while acquiring CD11b and CD43 by day 25.

B220 is a lineage associated– rather than an activation marker in the NK-cell differentiation pathway and defines pre-mNK cells. Guimont-Desrochers et al adoptively transferred various NK-cell subsets and followed their proliferation and phenotype in immunocompetent versus Rag1-deficient recipients treated or not with activating stimuli (known to up-regulate B220 molecules in vitro). While IKDCs remained B220 at early time points without activation (and maintained this expression at later time points after activation), B220 NK cells (expressing or not CD27) failed to acquire B220. The follow-up study of B220+ NK cells revealed that this subset differentiated into maturing NK cells over time, losing B220, Ly108, and CD27 while acquiring CD11b and CD43 by day 25.

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