Control of cytosolic free calcium in rat and chicken osteoclasts. The role of extracellular calcium and calcitonin

Single cell Ca2+], studies were performed in chicken and rat osteoclasts loaded with fura-2 and exposed to a variety of treatments. Under resting conditions, basal Ca2+]i, was 79.2 +/- 47.3 and 84.3 +/- 65.7 nM (averages +/- S.D.; n = 141 and 126) in the osteoclasts of the two species, respectively. Basal Ca2+]i was stable in all rat and in approximately 80% of chicken osteoclasts. In the remaining 20%, spontaneous, irregular Ca2+], fluctuations were observed (amplitude range: 50-200 nm over basal values). Increase of Ca2+]o over the concentration of the Krebs-Ringer incubation medium (2 mM) induced rises of Ca2+] in almost all cells investigated. Ca2+] rises were already appreciable with 0.5 mM Ca2+]o additions and reached high values with 4 mM additions: 390 +/- 113 and 364 +/- 214 nM Ca2+], in rat and chicken osteoclasts, respectively (n = 122 and 101). Qualitatively, the responses to Ca2+]o additions consisted of discrete Ca2+]i transients, biphasic (an initial spike followed by a plateau), or monophasic (either the spike or the plateau). In a few chicken osteoclasts, the Ca2+]i increase occurring after Ca2+]o addition consisted of multiple, irregular fluctuations, similar to those observed in 20% of these cells under resting conditions. In individual osteoclasts subsequently exposed to multiple Ca2+]o increase pulses, the type of the Ca2+]i transient (mono- or biphasic) was maintained, and the size was dependent on the magnitude of the Ca2+]o additions. Effects similar to those of Ca2+]o were induced by the addition of Cd2+ or Ba2+ (but not La3+ or Mg2+) into the medium. The Cd2+ effect was maintained in part even in a Ca2+-free medium. Of various hormones and factors, parathormone, 1,25-dihydroxyvitamin D3, and prostaglandin E2 were inactive. In contrast, calcitonin was active in rat osteoclasts (which express numerous receptors). Ca2+]i increases were small (19 +/- 17.9 nM; n = 21) when the hormone was administered alone; they were synergistic (severalfold potentiation) when the hormone was administered before or after Ca2+]o. The Ca2+]i effects of calcitonin were mimicked by 8Br-cAMP (31 +/- 26 nM; n = 12) when the nucleotide was administered alone; marked synergism when it was administered in combination with Ca2+]o. This paper demonstrates for the first time that changes of Ca2+]i are induced in osteoclasts by treatments with Ca2+]o and calcitonin and can therefore be involved in intracellular mediation of the physiological effects of these two extracellular signals.