PARATHYROID HORMONE-RELATED PROTEIN INCREASES DNA-SYNTHESIS IN PROXIMAL TUBULE CELLS BY CYCLIC AMP-DEPENDENT AND PROTEIN-KINASE C-DEPENDENTPATHWAYS

The present study was performed to characterize the possible involveme nt of cAMP synthesis and protein kinase C (PKC) activation in the DNA synthesis-stimulating effect of parathyroid hormone-related protein (P THrP) in proximal tubule cells. We found that DNA synthesis was stimul ated by 10 mu M 8BrcAMP, and 1 mu M Sp-cDBIMPS, two cAMP analogs, and also by 1 CIM phorbol 12-myristate 13-acetate (PMA) and 100 mu M 1,2-d ioctanoyl-sn-glycerol, two PKC activators, and 10 nM [Cys(23)] human ( h)PTHrP (24-35) amide in rabbit proximal tubule cells (PTC). Both Sp-c DBIMPS and PMA, at 1 CIM, also increased DNA synthesis in SV-40-immort alized mouse proximal tubule cells MCT. Human PTHrP (7-34) amide [PTHr P (7-34)] dose dependently stimulated DNA synthesis in a similar manne r as [(34)Tyr]PTHrP (1-34) amide [PTHrP (1-34)], in PTC. PMA pre-treat ment for 20 h, which downregulates PKC, completely blocked the effect induced by PTHrP (7-34), but not that of PTHrP (1-34), in the latter c ells. In contrast, the same PMA pre-treatment abolished the DNA synthe sis stimulation by PTHrP (1-34) and PTHrP (7-34) in MCT cells, which a ppear to have PTH receptors mainly coupled to phospholipase C and not adenylate cyclase. Our results indicate that the stimulatory effect of PTHrP on DNA synthesis in proximal tubule cells is mediated by a cAMP - and PKC-dependent mechanism.