Figure 1
Figure 1. Anti-β3 integrin antibodies were generated in β3−/−FcRn−/− mice after immunization with β3+/+FcRn−/− platelets. (A) β3+/+FcRn−/− mouse platelets were incubated with a 1:100 dilution of sera from β3−/−FcRn+/+ mice immunized either 2 (gray) or 4 (black) times weekly or preimmune sera (filled area) and stained with FITC-conjugated goat anti–mouse IgG or rat anti–mouse IgG1, IgG2a, IgG2b, or IgG3. (B) Thrombocytopenia was observed in β3+/+FcRn−/− mice after intraperitoneal injection of 25 μL of antisera from β3−/−FcRn−/− mice transfused either 2 times (▴) or 4 times (▾) with β3+/+FcRn−/− platelets. PBS (■) was used as a control. (C) 50 μL of mouse anti-β3 integrin sera (50 μL; from 4× transfused β3−/−FcRn−/− mice) or (D) IVIG (10 μL; 10%) were injected intraperitoneally into 6- to 8-week-old β3−/−FcRn−/− or β3−/−FcRn+/+ littermate mice. The concentration of retained IgG was determined. Adult β3−/−FcRn−/− mice cleared IgG rapidly compared with β3−/−FcRn+/+ mice. n = 3-5 in each group.

Anti-β3 integrin antibodies were generated in β3−/−FcRn−/− mice after immunization with β3+/+FcRn−/− platelets. (A) β3+/+FcRn−/− mouse platelets were incubated with a 1:100 dilution of sera from β3−/−FcRn+/+ mice immunized either 2 (gray) or 4 (black) times weekly or preimmune sera (filled area) and stained with FITC-conjugated goat anti–mouse IgG or rat anti–mouse IgG1, IgG2a, IgG2b, or IgG3. (B) Thrombocytopenia was observed in β3+/+FcRn−/− mice after intraperitoneal injection of 25 μL of antisera from β3−/−FcRn−/− mice transfused either 2 times (▴) or 4 times (▾) with β3+/+FcRn−/− platelets. PBS (■) was used as a control. (C) 50 μL of mouse anti-β3 integrin sera (50 μL; from 4× transfused β3−/−FcRn−/− mice) or (D) IVIG (10 μL; 10%) were injected intraperitoneally into 6- to 8-week-old β3−/−FcRn−/− or β3−/−FcRn+/+ littermate mice. The concentration of retained IgG was determined. Adult β3−/−FcRn−/− mice cleared IgG rapidly compared with β3−/−FcRn+/+ mice. n = 3-5 in each group.

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