Figure 3
Figure 3. MZB cells, not B1b cells, are responsible for rapidly induced IgM xenoantibody formation. (A) MACS-enriched CD19pos B cells from BALB/c nude spleens (left panel) were purified using FACS sorting into CD21highCD23low MZB cells (middle panel) and CD21negCD23neg B1b cells (right panel). Representative plots are shown from 3 identical experiments. (B) CB17 SCID mice were given 2 to 5 × 106 subset B cells intravenously on day 0, and 200 μL whole hamster blood on day 7. Serum IgM xenoantibody titers in an unreconstituted SCID mouse (left panel), a SCID mouse given CD19posCD21highCD23low MZB cells (middle panel), and a SCID mouse given CD19posCD21negCD23neg B1b cells (right panel). Representative plots are shown from 1 of 3 to 4 mice from 3 identical experiments.

MZB cells, not B1b cells, are responsible for rapidly induced IgM xenoantibody formation. (A) MACS-enriched CD19pos B cells from BALB/c nude spleens (left panel) were purified using FACS sorting into CD21highCD23low MZB cells (middle panel) and CD21negCD23neg B1b cells (right panel). Representative plots are shown from 3 identical experiments. (B) CB17 SCID mice were given 2 to 5 × 106 subset B cells intravenously on day 0, and 200 μL whole hamster blood on day 7. Serum IgM xenoantibody titers in an unreconstituted SCID mouse (left panel), a SCID mouse given CD19posCD21highCD23low MZB cells (middle panel), and a SCID mouse given CD19posCD21negCD23neg B1b cells (right panel). Representative plots are shown from 1 of 3 to 4 mice from 3 identical experiments.

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