Several features of activation of mouse peritoneal macrophages were elicited by 1-2-d exposure to submicrogram concentrations of anti-Mac-1 (M1/70), a rat monoclonal antibody that reacts with the alpha chain of complement receptor type 3 (Mac-1). The changes induced included enhanced capacity to secrete H2O2 when triggered with PMA, decreased secretion of proteins, increased expression of Ia antigen and decreased phagocytosis of particles. These changes closely resembled those induced by rIFN-gamma in type, extent, and time course. The concentration of M1/70 IgG resulting in 50% of the maximal activation of macrophage H2O2-releasing capacity averaged 0.18 +/- 0.03 micrograms/ml. This activation was not blocked by anti-FcR mAb, and could be reproduced with M18/2, a mAb against beta chain of Mac-1, suggesting that a direct ligation of Mac-1 with mAb was responsible for the activation. Neither depletion of T cells nor addition of neutralizing Abs to IFN-gamma or TNF-alpha prevented M1/70-mediated macrophage activation. Moreover, F(ab')2 of M1/70, or plating of macrophages on C3bi-coated surfaces, inhibited the activation of macrophages by rIFN-gamma. These findings suggest that Mac-1 (CR3) may play an important role in macrophage activation.
Article| March 01 1987
Activation of mouse peritoneal macrophages by monoclonal antibodies to Mac-1 (complement receptor type 3).
S D Wright
Online Issn: 1540-9538
Print Issn: 0022-1007
J Exp Med (1987) 165 (3): 733–749.
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A Ding, S D Wright, C Nathan; Activation of mouse peritoneal macrophages by monoclonal antibodies to Mac-1 (complement receptor type 3).. J Exp Med 1 March 1987; 165 (3): 733–749. doi: https://doi.org/10.1084/jem.165.3.733
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