Cellular uptake of coagulation factor VIII: Elusive role of the membrane-binding spikes in the C1 domain. (August 2017)

• Record Type: Journal Article
• Authors: Castro-Núñez, Lydia; Koornneef, Johanna M.; Rondaij, Mariska G.; Bloem, Esther; van der Zwaan, Carmen; Mertens, Koen; Meijer, Alexander B.; Meems, Henriet
• Is Part Of: International journal of biochemistry & cell biology. Volume 89(2017)
• Page Start: 34
• Page End: 41
• Publication Date: 2017-08
• Subjects: Factor VIII -- Low density lipoprotein receptor-related protein 1 -- Receptor-mediated endocytosis -- α2-macroglobulin -- Factor V; Biochemistry -- Periodicals; Cytology -- Periodicals; Biochemistry -- Periodicals; Cell Biology -- Periodicals; Biochimie -- Périodiques; Cytologie -- Périodiques; Biochimie; Cytologie; Biochemistry; Cytology; Ressource Internet (Descripteur de forme); Périodique électronique (Descripteur de forme); Periodicals; 572.05
• DOI: 10.1016/j.biocel.2017.05.027
• Languages: English
• ISSNs: 1357-2725

Abstract

Abstract: Low density lipoprotein receptor-related protein 1 (LRP1) is involved in the catabolism of many ligands, including factor VIII (FVIII) and alpha-2-macroglobulin (α2 M). Transfer of FVIII to LRP1 is currently believed to be preceded by pre-concentration on the cell surface, by interacting with a so far unidentified component. In the present study, we used confocal microscopy and flow cytometry to compare endocytosis of FVIII and α2 M using U87MG cells. The results show that α2 M is rapidly internalized and does not compete for LRP1 mediated internalization of FVIII. FVIII endocytosis did not occur in the presence of receptor-associated-protein (RAP), but FVIII remained visible as a striated fluorescent pattern at the cell borders. In the presence of Von Willebrand Factor (VWF), no FVIII was observed on or within the cells, suggesting that VWF blocks interaction with both cell surface and LRP1. The same dual inhibition has previously been observed for FVIII C1 domain directed monoclonal antibody KM33. Elimination of the KM33 epitope by replacing FVIII C1 residues 2091–2095 and 2155–2160 for the homologues from factor V (FV), however, did not impair FVIII endocytosis. These membrane spikes alone were insufficient for cellular uptake, because FV was neither internalized by U87MG cells nor capable of effectively competing for FVIII endocytosis. These results show that FVIII endocytosis is driven by interaction with LRP1, but at the same time involves the spikes in the C1 domain that have been implicated in lipid binding.