Chemokine stromal cell-derived factor-1α modulates VLA-4 integrin-mediated multiple myeloma cell adhesion to CS-1/fibronectin and VCAM-1

Abstract

AbstractThe chemokine stromal cell-derived factor-1α (SDF-1α) and its G-protein–linked receptor CXCR4 are involved in hematopoietic progenitor cell and lymphocyte migration. The integrin VLA-4 is a cell adhesion receptor for CS-1/fibronectin and VCAM-1 and constitutes one of the main adhesion receptors mediating myeloma cell adhesion to bone marrow (BM) stroma in multiple myeloma (MM). It is shown here that MM CD38hiCD45RA− BM cells and myeloma-derived cell lines expressed CXCR4 and displayed a moderate chemotactic response to SDF-1α. Because cell migration in response to SDF-1α might require a dynamic regulation of integrin function, it was investigated whether SDF-1α can modulate VLA-4 function on myeloma cells. SDF-1α rapidly and transiently up-regulated VLA-4–mediated myeloma cell adhesion to both CS-1/fibronectin and VCAM-1, which was inhibited by pertussis toxin and cytochalasin D, indicating the involvement of Gi protein downstream signaling and an intact cytoskeleton. Modulation of VLA-4–dependent myeloma cell adhesion by SDF-1α could contribute to the trafficking and localization of these cells in the BM microenvironment.