Minimal neutrophil migration and minimal lactoferrin release was observed in the absence of an antibody or in the presence of an anti-HER-2/neu IgG mAb (Fig. 1A and B), even though the experiments were performed with interferon-γ stimulated neutrophils that express FcγRI. To

confirm that tumour colony destruction in the presence of neutrophils and an FcαRIxHer-2/neu BsAb was neither dependent on tumour cell type nor TAA, we also performed experiments with A431 cells. These cells have a high expression of epidermal growth factor receptor (EGFR). No intact tumour colonies were observed after culturing A431 colonies for 24 h in the presence of anti-EGFR IgA mAb (Fig. 1F). Only neutrophils and debris were observed, strongly supporting that tumour cells had been destroyed in our 3D culture system (Fig. 1F, upper panel; inset). Similarly, massive neutrophil

buy FK506 migration was observed in 3D collagen assays with SW-948 colon carcinoma tumour colonies in the presence of an anti-EpCAM IgA mAb [23]. Of note, the initial contact of neutrophils with tumour cells was presumably at random. However, when IgA mAbs or FcαRI BsAbs are available, a positive feedback neutrophil migration loop is initiated, which will selleck chemicals llc not occur in the absence of mAbs or in the presence of IgG mAbs [21]. Signalling through either FcαRI or FcγR depends on an association with the FcR γ-chain that bears immunoreceptor tyrosine-based activation motifs (ITAMs) [22, 24]. Tethering the FcαRI and FcR γ-chain into a stable Non-specific serine/threonine protein kinase FcαRI–FcR γ-chain complex involves several other aspects, including crucial electrostatic

interactions that are absent in FcγRI/FcR γ-chain interactions [9, 22, 24-28]. Furthermore, it was demonstrated that signalling through FcαRI is enhanced as compared with FcγRI [9, 21, 28]. FcγRIIa, which is the major FcγR expressed by unstimulated neutrophils, bears a unique ITAM in its cytoplasmatic tail that initiates signalling pathways [29]. However, the FcγRIIa-ITAM does not mediate cytokine release [29]. As such, signalling through FcγR is either lower as compared with that through FcαRI or induces dissimilar functions, which likely account for the observed differences in neutrophil migration and activation. This presumably also underlies the enhanced tumour cell killing after targeting FcαRI. In vivo, neutrophils need to extravasate from the bloodstream in order to enter tumours. We therefore investigated neutrophil migration in the presence of endothelial cells. HUVECs were grown as confluent monolayers on top of collagen gels that contained SK-BR-3 colonies. The presence of HUVECs increased neutrophil entry into collagen gels in either the absence or presence of antibody (Fig. 2A and B). This was not due to augmented acceleration of neutrophil migration, but the result of increased neutrophil infiltration (Fig. 2B). In the absence of antibody or in the presence of an anti-HER-2/neu IgG mAb, migration was random and no interaction with tumour colonies was observed.