Characterization of VLA-4-dependent myeloma cell adhesion to fibronectin and VCAM-1

The integrin VLA-4 mediates attachment of myeloma cells to multiple myeloma (MM) bone marrow stroma. The alternatively-spliced CS-1 region of fibronec tin (FN) and VCAM-1 are main ligands for VLA-4 and are both expressed on MM stroma. The Iii region is present in all FN isoforms and represents an add itional binding site for VLA-4. We employed FN fragments FN-H89 and FN-HO, that contain either the CS-1 and Hi, or only the Hi sites, respectively, as well as soluble VCAM-1 (sVCAM-1), to characterize VLA-4-mediated adhesion pathways used by myeloma cells to attach to MM stroma. CD38(high)CD45RA(-) cells from MM bone marrow, and the myeloma-derived cell lines NCI-H929, IM- 9 and RPMI 8226, specifically adhered, by different degrees, to FN-H89, FN- HO and sVCAM-1, and their VLA-4-dependent adhesion was substantially up-reg ulated by the anti-beta 1 antibody TS2/16, which increases the affinity of VLA-beta 1 integrins. Furthermore, VLA-4 function on NCI-H929 cells was enh anced by TS2/16 during adhesion to MM stroma. The alpha 4 beta 7 integrin m ediated a small portion of myeloma cell line adhesion to FN-H89, mainly upo n integrin activation with Mn2+. These results indicate that myeloma cells use VLA-4 to interact with CS-1/FN, H1/FN and VCAM-1 on MM stroma, and that its function can be potentially upregulated, enabling higher degrees of ce ll adhesion to these VLA-4 ligands, which might influence myeloma cell loca lization in the bone marrow.