In mineralising tissues such as growth plate cartilage extracellular organelles derived from the chondrocyte membrane are present. These matrix vesicles (MV) possess membrane transporters that accumulate Ca2+ and inorganic phosphate (P-i), and initiate the formation of hydroxyapatite crystals. MV are also present in articular cartilage, and hydroxyapatite crystals are believed to promote cartilage degradation in osteoarthritic joints. In the present study, P-i transport pathways in isolated bovine articular chondrocytes have been characterised. P-i uptake was temperature-sensitive and could be resolved into Na+-dependent and Na+-independent components. The Na+-dependent component saturated at high concentrations of extracellular P-i, with a K-m for P-i of 0.17mM. In solutions lacking Na+, uptake did not fully saturate, implying that under these conditions carrier-mediated uptake is supplemented by a diffusive pathway. Both Na+-dependent and Na+-independent components were sensitive to the P-i transport inhibitors phosphonoacetate and arsenate, although a fraction of Na+-independent P-i uptake was resistant to these anions. Total P-i uptake was optimal at pH 7.4, and reduced as pH was made more acidic or more alkaline, an effect that represented reduced Na+-dependent influx. RT-PCR analysis confirmed that two members of the NaPi III family, Pit-1 and Pit-2, are expressed, but that NaPi II transporters are not.