| First Author | Peng W | Year | 2011 |
| Journal | Biochem Biophys Res Commun | Volume | 407 |
| Issue | 3 | Pages | 466-71 |
| PubMed ID | 21406181 | Mgi Jnum | J:171933 |
| Mgi Id | MGI:5002415 | Doi | 10.1016/j.bbrc.2011.03.035 |
| Citation | Peng W, et al. (2011) RGD-containing ankyrin externalized onto the cell surface triggers alpha(V)beta(3) integrin-mediated erythrophagocytosis. Biochem Biophys Res Commun 407(3):466-71 |
| abstractText | The RGD motif on the extracellular matrix or cell surface, together with its integrin receptors, constitutes a major recognition system for cell adhesion. There are several erythrocyte major membrane skeletal proteins, e.g., alpha spectrin, ankyrin, and protein 4.2, that bear an RGD motif. However, it is not known whether the RGD/integrin recognition system is utilized in the erythrocyte-macrophage adhesion during erythrophagocytosis. Here we report that the RGD motif of ankyrin, but not others, is recognized by the alpha(v)beta(3) integrin receptor. In addition, the RGD motif of ankyrin, a peripheral membrane protein, can be externalized onto the cell surface when erythrocytes are incubated with calcium and sheared both at physiological levels. Furthermore, the erythrocyte-macrophage adhesion can be specifically inhibited by ankyrin and/or alpha(v)beta(3). Thus, externalization of ankyrin followed by RGD/integrin recognition may be a novel mechanism by which erythrocytes adhere to macrophages preceding phagocytosis. |
