CYTOSOLIC FREE CALCIUM CONCENTRATIONS IN AVIAN GROWTH PLATE CHONDROCYTES

Isolated avian growth plate chondrocytes convert the acetoxymethyl ester (AM) form of Fura-2 quickly and efficiently to the Ca2+-sensitive pentacarboxylic acid (FA) form. Control experiments indicate that the Kd for intracellular Fura-2 FA is very close to that of extracellular Fura-2 FA at the same ionic strength and pH and that the Fura-2 FA fluorescence from indicator converted by intracellular organelles is quite small. Correcting for the effects of extracellular Fura-2 FA and partial hydrolysis products has improved the accuracy of determination of intracellular [Ca2+] over earlier measurements in chondrocytes. Cytosolic [Ca2+] in isolated growth plate chondrocytes (containing cells from each maturational stage) is found to require approximately 9 hours to recover from the isolation process. After this recovery period, cytosolic [Ca2+] in these cells converges to approximately 70 nM regardless of the [Ca2+] of the recovery medium, suggesting regulation of cytosolic [Ca2+] to a set point. Chondrocytes that are separated into maturationally distinct fractions using countercurrent centrifugal elutriation show an increase in cytosolic [Ca2+] with cellular maturation. The least mature resting cells have a [Ca2+] near 57 nM, while the most mature hypertrophic cells are around 95 nM. © 1990.