MODULATION OF SEROTONIN UPTAKE KINETICS BY IONS AND ION GRADIENTS IN HUMAN PLACENTAL BRUSH-BORDER MEMBRANE-VESICLES

The modulation of serotonin uptake kinetics by Na+, Cl−, H+, and K+ was investigated in brush-border membrane vesicles prepared from normal human term placentas. The presence of Na+ and Cl− in the external medium was mandatory for the function of the serotonin transporter. In both cases, the initial uptake rate of serotonin was a hyperbolic function of the ion concentration, indicating involvement of one Na+ and one Cl− per transport of one serotonin molecule. The apparent dissociation constant for Na+ and Cl− was 145 and 79 mM, respectively. The external Na+ increased the Vmax of the transporter and also increased the affinity of the transporter for serotonin. The external Cl− also showed similar effects on the Vmax and the Kt, but its effect on the Kt was small compared to that of Na+. The presence of an inside-acidic pH, with or without a transmembrane pH gradient, stimulated the NaCl-dependent serotonin uptake. The effect of internal [H+] on the transport function was to increase the Vmax and decrease the affinity of the transporter for serotonin. The presence of K+ inside the vesicles also greatly stimulated the initial rates of serotonin uptake, and the stimulation was greater at pH 7.5 than at pH 6.5. This stimulation was a hyperbolic function of the internal K+ concentration at both pH values, indicating involvement of one K+ per transport of one serotonin molecule. The apparent dissociation constant for K+ was 5.6 mM at pH 6.5 and 4.0 mM at pH 7.5. The effects of internal [K+] on the uptake kinetics were similar to those of internal [H+]. It increased the Vmax but decreased the affinity for the transporter for serotonin. In addition, the effects of internal [H+] on the kinetic parameters were masked by the presence of K+ inside the vesicles, indicating competition between internal K+ and internal H+. © 1990, American Chemical Society. All rights reserved.