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Abstract

The selective increase of net K⁺ permeability in human red cells brought about by either Ca²⁺ or lead was studied using a light scattering technique to measure net K⁺ fluxes in cell suspensions and the patch-clamp technique to study K⁺ transport in individual K⁺-selective channels of the red cell membrane. Using ultrapure solutions it was demonstrated that the effect of lead is neither the indirect consequence of a lead-induced increase of the accessibility of the receptor sites of the K⁺-selective channels to traces of Ca²⁺ that are present as contamination in analytical grade reagents nor to the release of Ca²⁺ from intracellular Ca²⁺ stores. It is further shown that in cell-free membrane patches low concentrations of lead (10 μM) in Suprapur solutions evoke the same single-channel events as added Ca²⁺ and that this activity can be inhibited by high concentrations of lead (100 μM), similar to the net KCl efflux measured by means of the light scattering technique. It is concluded, therefore, that both Ca²⁺ and lead independently activate the same K⁺-selective channels in the red cell membrane.