Mn2+ regulates myeloma cell adhesion differently than the proadhesive cytokines HGF, IGF‐1, and SDF‐1α

• Published in: European journal of haematology Vol. 81; no. 6; pp. 437 - 447
• Main Authors: Slørdahl, Tobias S., Hov, Håkon, Holt, Randi U., Baykov, Vadim, Syversen, Tore, Sundan, Anders, Waage, Anders, Børset, Magne
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.12.2008
• Subjects: adhesion; divalent cations; hepatocyte growth factor; insuline‐like growth factor‐1; integrins; Mn2; multiple myeloma; stromal cell‐derived factor‐1α; very late antigen‐4
• ISSN: 0902-4441; 1600-0609
• DOI: 10.1111/j.1600-0609.2008.01148.x

Adhesion of multiple myeloma (MM) cells in the bone marrow (BM) is important for the growth and survival of the myeloma cells. Very late antigen‐4 (VLA‐4) is one of the main adhesion receptors that mediate MM cell binding to fibronectin (FN). In this study we have examined the effect of divalent cations on adhesion of MM cells to FN, and compared this type of adhesion with the adhesion induced by the cytokines HGF, IGF‐1 and SDF‐1α. Mn2+ induced adhesion in all cell lines tested. Cytokine‐ and Mn2+‐induced VLA‐4‐mediated adhesion were different in many respects, including binding specificity, adhesion kinetics and the activation state of VLA‐4. To study a potential role of divalent cations in vivo, we measured the concentrations of divalent cations in BM plasma from 14 MM patients. We also found that Mn2+‐mediated adhesion to FN activated the MAPK pathway, indicating that the interaction of MM‐cells with FN mediated by Mn2+ could play a critical role for growth and proliferation. In conclusion, this study shows a potential important role of divalent cations in MM cell biology and supports earlier studies pointing to activated VLA‐4 as a key for homing of MM cells to the BM.