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The Journal of Immunology, Vol 130, Issue 3 1210-1214, Copyright © 1983 by American Association of Immunologists
ARTICLES |
SN Vogel, DS Finbloom, KE English, DL Rosenstreich and SG Langreth
Previous studies demonstrated that the augmentation of Fc receptor- (FcR) mediated phagocytosis and binding of opsonized sheep erythrocytes is cytokine mediated. Specifically, beta-interferon- (beta-IFN) and gamma-IFN-rich preparations were shown to increase binding and phagocytosis of opsonized erythrocytes by C3H/HeJ macrophages. In this report we extend these studies by examination of the mechanisms by which highly purified beta-IFN increases FcR capacity in C3H/HeJ macrophages. Our findings indicate that beta-IFN augments FcR function for both IgG2a and IgG2b receptor subclasses. Moreover, this increased ability to bind and phagocytose opsonized erythrocytes is associated with a concomitant increase in both the number and surface membrane density of FcR.
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