Stimulation of transient elevations in cytosolic Ca²⁺ is related to inhibition of P(i) transport in OK cells

Stimulation of changes in cytosolic free calcium by parathyroid hormone was determined in three opossum kidney (OK) cell types, OK wild-type, OKP clone, and OKH clone. All three types of OK cells express parathyroid hormone (PTH)-sensitive adenylate cyclase and adenosine 3',5'-cyclic monophosphate (cAMP) production. However, only the OK wild-type and the OKP clone respond to PTH with inhibition of sodium-dependent P(i) transport and transient increases in cytosolic calcium. Characterization of the increases in cytosolic calcium in the wild-type and OKP clones revealed they were due in part to stimulation of Ca²⁺ release from intracellular stores, probably by inositol 1,4,5-trisphosphate (IP₃), which was stimulated by PTH. PTH-stimulated Ca²⁺ transients were also inhibited by protein kinase C activation. These data are compatible with PTH receptor-mediated phospholipase C activation and its feedback inhibition by protein kinase C. The OKH cells demonstrated a slow increase in cytosolic calcium when stimulated by cyclic nucleotides but no evidence for PTH stimulation of Ca²⁺ release from intracellular stores. Thus the absence of an inhibitory response of sodium-dependent P(i) transport to PTH in the OKH cells is associated with the absence of the rapid transient elevations of cytosolic Ca²⁺ such as those produced by IP₃ production. These data suggest an important cooperative role for cAMP and the phospholipase C-stimulated Ca²⁺-protein kinase C message system in the regulation of P(i) transport.