Figure 6.
Figure 6. Recycling of IgG is not responsible for enhanced phagocytosis mediated by FcRn. (A) Effect of IgG level on phagocytosis of pneumococci by wild-type and β2M-/- mouse PMNs. Note that phagocytosis by β2M-/- PMNs is more impaired at higher concentrations of human IgG1. (B) Recycling of human IgG1 by wild-type and β2M-/- mouse PMNs. Wild-type mouse PMNs and β2M-/- PMNs were allowed to take up human IgG1 antiserotype 6B mAb (10 μg/mL) for 5 minutes at 37°C in the presence of serotype 6B pneumococci. After extensive washing, cells were incubated for an additional 30 minutes in medium to allow for exocytosis/recycling of IgG, and supernatants were subsequently analyzed for the presence of human anti-6B pneumococcal antibodies by ELISA. Control samples in which mouse PMNs were incubated with IgG1 only (without bacteria) did not result in significant recycling. Experiments were repeated 4 times, with essentially identical results. Data represent means plus or minus standard deviation.

Recycling of IgG is not responsible for enhanced phagocytosis mediated by FcRn. (A) Effect of IgG level on phagocytosis of pneumococci by wild-type and β2M-/- mouse PMNs. Note that phagocytosis by β2M-/- PMNs is more impaired at higher concentrations of human IgG1. (B) Recycling of human IgG1 by wild-type and β2M-/- mouse PMNs. Wild-type mouse PMNs and β2M-/- PMNs were allowed to take up human IgG1 antiserotype 6B mAb (10 μg/mL) for 5 minutes at 37°C in the presence of serotype 6B pneumococci. After extensive washing, cells were incubated for an additional 30 minutes in medium to allow for exocytosis/recycling of IgG, and supernatants were subsequently analyzed for the presence of human anti-6B pneumococcal antibodies by ELISA. Control samples in which mouse PMNs were incubated with IgG1 only (without bacteria) did not result in significant recycling. Experiments were repeated 4 times, with essentially identical results. Data represent means plus or minus standard deviation.

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