Bone resorption induced by 1 alpha,25 dihydroxyvitamin D-3 in vivo is not altered by inactivation of the plasminogen activator inhibitor 1

One of the proteolytic systems produced by bone cells is the plasminogen ac tivator/plasmin pathway, which involves the two plasminogen activators and the type 1 plasminogen activator inhibitor (PAI-1) and results in plasmin g eneration. We have recently demonstrated that this pathway plays a specific role in the degradation of the nonmineralized matrix of bone in vitro. To evaluate whether PAI-1 is required during bone resorption in vivo, we studi ed the effects of PAI-1 inactivation on bone metabolism using systemic admi nistration of 1 alpha,25 dihydroxyvitamin D-3 [1,25(OH)(2)D-3] as model. PA I-1-deficient (PAI-1-/-) and wild-type (WT) mice were injected intraperiton eally with 1,25(OH)(2)D-3 (2 mu g/kg) or vehicle every other day during 4 w eeks and analyzed using biochemical parameters of bone turnover, histomorph ometric analysis of the proximal tibial metaphysis, and pQCT analysis of th e distal femoral metaphysis. PAI-1 inactivation did not affect bone metabol ism in vehicle-treated mice. Treatment with 1,25(OH)(2)D-3 induced bone res orption similarly in PAI-1-/- and WT mice, as assessed by the increase in t he urinary excretion of calcium (2.2-fold and 2.3-fold, respectively) and o f pyridinoline crosslinks (by 24% and 22%, respectively). In addition, a co mparable reduction in bone mass was observed in PAI-1-/- and WT mice after treatment with 1,25(OH)(2)D-3, as evidenced by the decrease in the femoral calcium content (by 25% and 32%, respectively), in the trabecular bone volu me (by 50% and 40%, respectively), in the trabecular mineral content (by 17 % and 15%, respectively), and in the cortical mineral content (by 45% and 5 2%, respectively). The parameters of bone turnover also increased after 1,2 5(OH)(2)D-3 treatment. Serum osteocalcin was, respectively, 25% and 28% hig her in PAI-1-/- and WT mice treated with 1,25(OH)(2)D-3 compared with the m ice injected with vehicle. Similarly, the osteoid surface increased in 1,25 (OH)(2)D-3-treated PAI-1-/- and WT mice by 40% and 51%, respectively, the m ineral apposition rate increased by 15% and 8%, respectively, and the bone formation rate by 54% and 48%, respectively. These data indicate that PAI-1 is not critical during bone resorption induced by 1,25(OH)(2)D-3 in vivo. (Bone 27:97-102; 2000) (C) 2000 by Elsevier Science Inc. All rights reserve d.