Localization of five annexins in J774 macrophages and on isolated phagosomes

• Published in: Journal of cell science Vol. 110 ( Pt 10); no. 10; pp. 1199 - 1213
• Main Authors: Diakonova, M, Gerke, V, Ernst, J, Liautard, J P, van der Vusse, G, Griffiths, G
• Format: Journal Article
• Language: English
• Published: England 01-05-1997
• Subjects: Animals; Annexin A1 - metabolism; Annexin A2 - metabolism; Annexin A3 - metabolism; Annexin A4 - metabolism; Annexin A5 - metabolism; Annexins - metabolism; Cell Line; Cell Membrane - metabolism; Immunohistochemistry; Macrophages - metabolism; Macrophages - ultrastructure; Mice; Microscopy, Confocal; Microscopy, Electron; Microscopy, Immunoelectron; Organelles - metabolism; Phagocytosis; Phagosomes - metabolism; Phagosomes - ultrastructure
• ISSN: 0021-9533; 1477-9137
• DOI: 10.1242/jcs.110.10.1199

Annexins are a family of structurally related proteins which bind phospholipids in a calcium-dependent manner. Although the precise functions of annexins are unknown, there is an accumulating set of data arguing for a role for some of them in vesicular transport and, specifically, in membrane-membrane or membrane-cytoskeletal interactions during these processes. Here we describe our qualitative and quantitative analysis of the localization of annexins I-V in J774 macrophages that had internalized latex beads, both with and without IgG opsonization. Our results show that whereas all these annexins are present on both the plasma membrane and on phagosomes, the localization on other organelles differs. Annexins I, II, III and V were detected on early endosomes, while only annexin V was seen on late endocytic organelles and mitochondria. Annexins I and II distributed along the plasma membrane non-uniformly and co-localized with F-actin at the sites of membrane protrusions. We also investigated by western blot analysis the association of annexins with purified phagosomes isolated at different time-points after latex bead internalization. While the amounts of annexins I, II, III and V associated with phagosomes were similar at all times after their formation, the level of annexin IV was significantly higher on older phagosomes. Whereas annexins I, II, IV and V could be removed from phagosome membranes with a Ca2+ chelator they remained membrane bound under low calcium conditions. In contrast, annexin III was removed under these conditions and needed a relatively high Ca2+ concentration to remain phagosome bound. Because of their purity and ease of preparation we suggest that phagosomes are a powerful system to study the potential role of annexins in membrane traffic.