Fig. 4.
Fig. 4. More rapid clearance of membrane complement regulator–deficient erythrocytes by the complement than by the FcR pathway. / Biotin-labeled Crry/DAF/C3−/− erythrocytes (3 × 108 per recipient) were either opsonized (+) or not (−) with 50 μg/mL mAb 34-3C, and transfused into FcγR−/− mice (complement-mediated pathway) or C3−/− mice (FcR-dependent pathway). The number of biotin-positive cells (expressed as percentage of total cells) in the recipient mice (n = 4 in FcγR−/− mice experiment; n = 6 and n = 7 for antibody-sensitized and nonsensitized, respectively, in C3−/− mice experiment) at 5 minutes (filled bars) and 3 hours (hatched bars) was determined. Very few of the antibody-opsonized cells were recovered from FcγR−/− mice at 5 minutes and almost none at 3 hours. In contrast, a high percentage of the antibody-opsonized cells remained in the circulation of C3−/− mice at 5 minutes and 3 hours. Error bars indicate means ± SE.

More rapid clearance of membrane complement regulator–deficient erythrocytes by the complement than by the FcR pathway.

Biotin-labeled Crry/DAF/C3−/− erythrocytes (3 × 108 per recipient) were either opsonized (+) or not (−) with 50 μg/mL mAb 34-3C, and transfused into FcγR−/− mice (complement-mediated pathway) or C3−/− mice (FcR-dependent pathway). The number of biotin-positive cells (expressed as percentage of total cells) in the recipient mice (n = 4 in FcγR−/− mice experiment; n = 6 and n = 7 for antibody-sensitized and nonsensitized, respectively, in C3−/− mice experiment) at 5 minutes (filled bars) and 3 hours (hatched bars) was determined. Very few of the antibody-opsonized cells were recovered from FcγR−/− mice at 5 minutes and almost none at 3 hours. In contrast, a high percentage of the antibody-opsonized cells remained in the circulation of C3−/− mice at 5 minutes and 3 hours. Error bars indicate means ± SE.

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