Affiliations: Universidad Tecnológica de Pereira, Departamento de Ciencias Básicas, Facultad de Ciencias de la Salud, A.A. 97, La Julita, Pereira, Risaralda, Colombia | University Laboratory of Physiology, Parks Road, Oxford, OX1 3PT, United Kingdom
Note: [] Address for correspondence: Dr. R.J. Wilkins, University Laboratory of Physiology, Parks Road, Oxford OX1 3PT, United Kingdom. Tel.: +44 1865 285829; Fax: +44 1865 272488; E-mail: [email protected].
Abstract: Altered fluxes of Ca2+ across the chondrocyte membrane have been proposed as one pathway by which mechanical load can modulate cartilage turnover. In many cells, Na+/Ca2+ exchange (NCX) plays a key role in Ca2+ homeostasis, and recent studies have suggested it is operative in articular chondrocytes. In this study, an electrophysiological characterisation of NCX in articular bovine chondrocytes has been performed, using the whole-cell patch clamp technique, and the effects of inhibitors and the transmembrane electrochemical gradients of Na+ and Ca2+ on NCX function have been assessed. A Ni2+-sensitive current (INCX) which exhibited outward rectification, was elicited by a voltage ramp protocol. The current was also attenuated by the NCX inhibitors benzamil and KBR7943, without significant differences between the effect of these two compounds upon outward and inward currents. The Ni2+-sensitive current was modulated by changes in extracellular and pipette Na+ and Ca2+ in a manner characteristic of \[$I\tsub{NCX}$. Measured values for the reversal potential differed significantly from those predicted for an exchanger stoichiometry of 3Na+ : 1Ca2+, implying that accumulation of intracellular Ca2+ (from influx or release from stores) or more than one transport mode is occurring. These results demonstrate the operation of NCX in articular chondrocytes and suggest that changes in its turnover rate, as might occur in response to mechanical load, may modify cell composition and thereby dictate cartilage turnover.
