Receptors For Third Component Research Articles

Establishment of T-cell hybridoma constitutively producing macrophage-dependent T-cell replacing factor

A T-cell hybridoma was established by the fusion of concanavalin A-stimulated splenic T cells with BW 5147. The hybridoma cells secrete a factor constitutively to support antibody formation of spleen cells depleted of T cells against TNP-Ficoll but not against horse red blood cells. The activity was indicated not to be due to interleukin 2, B-cell growth factor I, B-cell growth factor II, or interferon. The factor-mediated antibody response to TNP-Ficoll required the presence of adherent cells. The adherent cell function could be replaced by the macrophage culture supernatant containing interleukin 1. B cells responding to TNP-Ficoll in the culture with hybridoma factor were indicated to be Lyb 5 + and to bear receptors for third component of complement.

Antibody response of murine spleen cells with or without receptors for C3 to antigenic or mitogenic stimulation

Bone marrow-derived lymphocytes (B cells) with or without receptors for third component of complement (CR) were studies in their responsiveness to T-independent antigens and B-cell mitogens in terms of anti-DNP PFC response. Spleen cells were fractionated by centrifugation over a Ficoll-Hypaque density gradient after they were rosetted with antigen-antibody-complement complexes. The cells in interface fraction could not respond to any T-independent antigen tested, while they responded well to polyclonal stimulations by lipopolysaccharide and polymerized flagellin but not by keyhole limpet hemocyanin. Reduced response to T-independent antigen of the cells in interface fraction could not be explained by a shift of the kinetics, lack of number of B cells, or by the depletion of macrophages. Significance of CR in B-cell differentiation is discussed.