Abstract

Rb + influx was used to assess NaKCl cotransport and Na,K-ATPase activities in cultured monkey retinal pigment epithelium. Bumetanide-sensitive (NaKCl cotransport-mediated) Rb + influx exceeds ouabain-sensitive (Na,K-ATPase-mediated) Rb + influx, with these two transporters accounting for ∼ 95% of total Rb + uptake. Half-maximal inhibition of Rb + influx by bumetanide is attained at 75 n m bumetanide. The bumetanide-sensitive Rb + influx depends on both extracellular Na + and Cl −, and is activated by extracellular Rb + with a relatively high affinity. NaKCl cotransport activity is stimulated (2·5-fold) by increased extracellular osmolarity. Elevated cAMP content and glycolytic inhibition both depress cotransport activity. Cyanide application, however, had very little effect on NaKCl cotransport activity. Monkey retinal pigment epithelial cells, maintained in culture, provide a system in which the activity and regulation of cation transport mechanisms can be examined.

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