Osteoblastic cells have been shown to be involved in osteoclast formation through cell to cell contacts. This study was designed to examine the possible function of vascular cell adhesion molecule 1 (VCAM-1) during osteoclastogenesis, As a source for stromal cells we used the recently established mouse bone marrow stromal cell line mBMS-B1 which has the ability to support osteoclastogenesis when used in co-culture with a crude spleen cell suspension, mBMS-B1 cells express a single similar to 3.9 kb VCAM-1 mRNA species, Expression was low under basal culture conditions and a 5-10-fold increase was observed in the presence of 1,25(OH)(2)D-3. Cell surface expression of VCAM-1 examined by FACS analysis was increased about 2-fold after 1,25(OH)(2)D-3 treatment, Immunoprecipitation of cell surface expressed VCAM-1 or total VCAM-1 protein using the anti-VCAM-1 monoclonal antibody MK2.7 resulted in a single similar to 110 kDa protein on SDS-PAGE, Induction by 1,25(OH)(2)D-3 was about 2-5-fold on day 3, The stromal cell-osteoclast precursor cell interaction was investigated in a co-culture of the mBMS-B1 and mouse spleen cells in the presence of 1,25(OH)(2)D-3, The monoclonal antibody MK2.7 which is known to block hemopoietic-stromal cell recognition inhibited the formation of osteoclasts when added to the co-culture at day 2 but not day 4, These data suggest that VCAM-1 is involved in the interaction between stromal cells and osteoclastic precursor cells during osteoclastogenesis presumably most important during early stages of the formation of osteoclasts.