Bisphosphonates modulate the effect of macrophage-like cells on osteoblast

Macrophages (MPs) are present in many tissues and have been implicated in the excessive bone resorption seen in patients with skeletal disorders. Our previous studies showed that macrophage-like cells influenced osteoblasts (OB) in co-culture. as number and activity of osteoblasts were decreased in co-cultures compared with controls. Macrophages ire probable precursors of osteoblasts which have been shown to be inhibited by bisphosphonates (BPs). Bisphosphonates also modulate macrophage and osteoblasts activity. This study investigated whether addition of bisphosphonates to co-cultures of osteoblast and macrophages could reduce or block the adverse effect of macrophages on osteoblasts. The results showed that, compared to controls, fewer osteoblasts were present overtime in macrophage/osteoblast co-cultures (at day 12.15.5 x 10(4) and 8.8 x 10(4). P < 0.0001) and that addition of bisphosphonates ( 10(-9)-10(-5) M) to the co-cultures prevented this reduction ( P < 0.001). Bisphosphonates also elicited an increase in numbers of osteoblast (82%) and restored alkaline phosphatase (ALP) activity, which was reduced by 15% (P congruent to 0.05) compared to control levels. The number of macrophages in co-cultures was reduced when bisphosphonates were added ( P < 0.001) and release of lactate dehydrogenase (LDH) was seen, which was not detectable in control cultures. It therefore. appears that bisphosphonates initiated macrophage death. These results demonstrated that the inhibitory effect of macrophages on osteoblasts in vitro could be overcome by the action of bisphosphonates. These findings have implications for the treatment of skeletal conditions where macrophage-derived cytokines are important. Such as arthritis and implant loosening, although it is clearly important to distinguish between those bisphosphonates which enhance synthesis of pro-inflammatory cytokines and those which inhibit such synthesis. (C) 2002 Elsevier Science Ltd, All rights reserved.