Parathyroid hormone prevents 1,25(OH)(2)D-3 induced down-regulation of the vitamin D receptor in growth plate chondrocytes in vitro

1,25(OH)(2)D-3 has an antiproliferative effect on growth plate chondrocytes when given in high doses, whereas low doses stimulate chondrocyte proliferation. In the present in vitro study we investigated the effects of parathyroid hormone (PTH) when given concomitantly with 1,25(OH)(2)D-3 on cell proliferation and vitamin D receptor (VDR) regulation Freshly isolated rat tibial chondrocytes were grown in monolayer cultures or in agarose stabilized suspension cultures (10% charcoal-treated FCS). VDR expression was determined by RT PCR generating a 297 bp fragment and by binding assays (Scatchard analysis) with [H-3]-1,25(OH)(2)D-3. Cell proliferation was measured by [H-3]-thymidine incorporation, growth curves in monolayer cultures and by colony formation in agarose-stabilized suspension cultures. Optimal concentration of 1,25(OH)(2)D-3 (10(-12) M) and of PTH fragments [bPTH(1-34) or hPTH(28-48), 10(-10) M] showed additive effects on DNA synthesis of and colony formation by growth plate chondrocytes. This may be explained in part by an up-regulation of VDR by PTH: PTH increased both mRNA expression of VDR and binding capacity. 1,25(OH)(2)D-3 (10(-12) mu M) induced an up-regulation of the VDR within 24 hours followed by a down-regulation after incubation for more than 24 hours. PTH fragments added concomitantly prevented the downregulation seen with 1,25(OH)(2)D-3. These findings provide evidence that PTH is a growth promoting hormone that also modulates the effects of 1,25(OH)(2)D-3 by regulating the VDR status of 1,25(OH)(2)D-3 target cells.